Psychological therapies for the management of chronic pain (excluding headache) in adults
Open accessAbstract
BACKGROUND: Chronic non-cancer pain, a disabling and distressing condition, is common in adults. It is a global public health problem and economic burden on health and social care systems and on people with chronic pain. Psychological treatments aim to reduce pain, disability and distress. This review updates and extends its previous version, published in 2012. OBJECTIVES: To determine the clinical efficacy and safety of psychological interventions for chronic pain in adults (age > 18 years) compared with active controls, or waiting list/treatment as usual (TAU). SEARCH METHODS: We identified randomised controlled trials (RCTs) of psychological therapies by searching CENTRAL, MEDLINE, Embase and PsycINFO to 16 April 2020. We also examined reference lists and trial registries, and searched for studies citing retrieved trials. SELECTION CRITERIA: RCTs of psychological treatments compared with active control or TAU of face-to-face therapies for adults with chronic pain. We excluded studies of headache or malignant disease, and those with fewer than 20 participants in any arm at treatment end. DATA COLLECTION AND ANALYSIS: Two or more authors rated risk of bias, extracted data, and judged quality of evidence (GRADE). We compared cognitive behavioural therapy (CBT), behavioural therapy (BT), and acceptance and commitment therapy (ACT) with active control or TAU at treatment end, and at six month to 12 month follow-up. We did not analyse the few trials of other psychological treatments. We assessed treatment effectiveness for pain intensity, disability, and distress. We extracted data on adverse events (AEs) associated with treatment. MAIN RESULTS: We added 41 studies (6255 participants) to 34 of the previous review's 42 studies, and now have 75 studies in total (9401 participants at treatment end). Most participants had fibromyalgia, chronic low back pain, rheumatoid arthritis, or mixed chronic pain. Most risk of bias domains were at high or unclear risk of bias, with selective reporting and treatment expectations mostly at unclear risk of bias. AEs were inadequately recorded and/or reported across studies. CBT The largest evidence base was for CBT (59 studies). CBT versus active control showed very small benefit at treatment end for pain (standardised mean difference (SMD) -0.09, 95% confidence interval (CI) -0.17 to -0.01; 3235 participants; 23 studies; moderate-quality evidence), disability (SMD -0.12, 95% CI -0.20 to -0.04; 2543 participants; 19 studies; moderate-quality evidence), and distress (SMD -0.09, 95% CI -0.18 to -0.00; 3297 participants; 24 studies; moderate-quality evidence). We found small benefits for CBT over TAU at treatment end for pain (SMD -0.22, 95% CI -0.33 to -0.10; 2572 participants; 29 studies; moderate-quality evidence), disability (SMD -0.32, 95% CI -0.45 to -0.19; 2524 participants; 28 studies; low-quality evidence), and distress (SMD -0.34, 95% CI -0.44 to -0.24; 2559 participants; 27 studies; moderate-quality evidence). Effects were largely maintained at follow-up for CBT versus TAU, but not for CBT versus active control. Evidence quality for CBT outcomes ranged from moderate to low. We rated evidence for AEs as very low quality for both comparisons. BT We analysed eight studies (647 participants). We found no evidence of difference between BT and active control at treatment end (pain SMD -0.67, 95% CI -2.54 to 1.20, very low-quality evidence; disability SMD -0.65, 95% CI -1.85 to 0.54, very low-quality evidence; or distress SMD -0.73, 95% CI -1.47 to 0.01, very low-quality evidence). At follow-up, effects were similar. We found no evidence of difference between BT and TAU (pain SMD -0.08, 95% CI -0.33 to 0.17, low-quality evidence; disability SMD -0.02, 95% CI -0.24 to 0.19, moderate-quality evidence; distress SMD 0.22, 95% CI -0.10 to 0.54, low-quality evidence) at treatment end. At follow-up, we found one to three studies with no evidence of difference between BT and TAU. We rated evidence for all BT versus active control outcomes as very low quality; for BT versus TAU. Evidence quality ranged from moderate to very low. We rated evidence for AEs as very low quality for BT versus active control. No studies of BT versus TAU reported AEs. ACT We analysed five studies (443 participants). There was no evidence of difference between ACT and active control for pain (SMD -0.54, 95% CI -1.20 to 0.11, very low-quality evidence), disability (SMD -1.51, 95% CI -3.05 to 0.03, very low-quality evidence) or distress (SMD -0.61, 95% CI -1.30 to 0.07, very low-quality evidence) at treatment end. At follow-up, there was no evidence of effect for pain or distress (both very low-quality evidence), but two studies showed a large benefit for reducing disability (SMD -2.56, 95% CI -4.22 to -0.89, very low-quality evidence). Two studies compared ACT to TAU at treatment end. Results should be interpreted with caution. We found large benefits of ACT for pain (SMD -0.83, 95% CI -1.57 to -0.09, very low-q
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TL;DR
This Cochrane review found that cognitive behavioural therapy (CBT) has small-to-moderate benefits for chronic pain in adults, especially compared with treatment as usual or waiting list, while evidence for behaviour therapy is weak and sparse. Effects were strongest for mood and catastrophic thinking, with smaller effects on disability and pain.
Key findings
- The review included 42 trials; 35 provided usable data, with 4788 treated participants providing post-treatment data from 5424 starting treatment. Mean study quality was 21.2/35 overall, 15.8/26 for design, and 5.4/9 for treatment quality.
- CBT versus active control: disability improved post-treatment (SMD -0.19, 95% CI -0.33 to -0.05; 12 studies, 1130 participants) and at follow-up (SMD -0.15, 95% CI -0.28 to -0.02; 12 studies, 1295 participants); catastrophising improved post-treatment (SMD -0.18, 95% CI -0.36 to 0.00; 6 studies, 735 participants). Pain and mood were not significant.
- CBT versus treatment as usual/waiting list: significant post-treatment effects were found for pain (SMD -0.21, 95% CI -0.37 to -0.05; 16 studies, 1148 participants), disability (SMD -0.26, 95% CI -0.47 to -0.04; 15 studies, 1105 participants), mood (SMD -0.38, 95% CI -0.57 to -0.18; 12 studies, 899 participants), and catastrophising (SMD -0.53, 95% CI -0.76 to -0.31; 5 studies, 308 participants). At follow-up, only mood was just significant (SMD -0.26, 95% CI -0.51 to 0.00; 7 studies, 637 participants).
- Behaviour therapy versus treatment as usual showed no significant post-treatment effects on pain, disability, or mood; catastrophising was just significant (SMD -0.72, 95% CI -1.43 to -0.01; 3 studies, 269 participants) but with high heterogeneity (I² = 84%). There were insufficient studies for meta-analysis of behaviour therapy versus active control.
Methods
- Systematic review and meta-analysis of RCTs in adults aged 18 years or older with non-malignant chronic pain of at least three months’ duration, excluding headache or migraine. Trials compared a credible psychological treatment with placebo, active treatment, treatment as usual, or waiting list control, and required at least 20 participants per treatment arm at post-treatment assessment.
- Searches covered CENTRAL, MEDLINE, EMBASE, and Psychlit from inception to September 2011, with no language restrictions. Two treatment classes were analysed: CBT and behavioural therapy; comparators were active control and treatment as usual/waiting list.
- Outcomes were pain, disability, mood, and catastrophic thinking at post-treatment and follow-up (at least six months and not more than 12 months after treatment). Treatment effects were estimated using standardised mean differences, with heterogeneity assessed by Chi² and I²; risk of bias and the Yates quality scale were applied.
Limitations
- The paper states that no data were available on adverse events, withdrawal and escape, or emergency analgesia; no dichotomous outcomes were reported, so no numbers needed to treat were calculated; no adjustment for reliability of measures was made; and planned subgroup analyses on doses and different conditions were not undertaken due to lack of data.
- The review reports high heterogeneity in many analyses, especially for behaviour therapy, and notes that most high risk-of-bias judgements were due to inadequate reporting. Treatment quality did not improve over time, and average effects may mask larger changes in some patients and little or none in others.
- Evident from the text: behaviour therapy comparisons were often based on only one or two studies, limiting power; control classification of treatment as usual/waiting list was described as not entirely satisfactory; and the review could not resolve whether the psychotherapeutic content of existing trials was adequate.
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- Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at post-treatment significantly improved disability (12 studies, 1130 participants; SMD -0.19, 95% CI -0.33 to -0.05; Z=2.66, P<0.01; I2=25%).
“We entered 12 studies with 1130 participants into an analysis of the effects of CBT on disability. The overall effect was significant (Z = 2.66, P < 0.01) with a small effect size: standardised mean difference (SMD) -0.19 (95% confidence interval (CI) -0.33 to -0.05) (Analysis 1.2); the I value was 25%.”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at follow-up significantly improved disability (12 studies, 1295 participants; SMD -0.15, 95% CI -0.28 to -0.02; Z=2.28, P<0.05; I2=23%).
“We entered 12 studies with 1295 participants into an analysis of the effects of CBT on disability at follow-up.The overall effect of CBT at followup was significant (Z = 2.28, P < 0.05) with a small effect size of SMD -0.15 (95% CI -0.28 to -0.02) (Analysis 2.2); the I value was 23%.”
Quote in the paperSubstantial claim - Findingown data
The mean overall quality of the 42 included studies was 21.2 (SD 5.9).
“For the 42 studies which met the inclusion criteria, the mean overall quality of the studies was 21.2 (SD 5.9, range 10 to 32).”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at post-treatment had no significant overall effect on mood (13 studies, 1256 participants; Z=0.72, P>0.05).
“We entered 13 studies with 1256 participants into an analysis of the effects of CBT on mood; the overall effect was not significant (Z = 0.72, P > 0.05) (Analysis 1.3).”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at follow-up had no significant overall effect on pain (11 studies, 1261 participants; Z=1.12, P>0.05).
“We entered 11 studies with 1261 participants into an analysis of the effects of CBT on pain at follow-up.The overall effect of CBT was not significant (Z = 1.12,P > 0.05) (Analysis 2.1).”
Quote in the paperSubstantial claim
- Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at post-treatment had no significant overall effect on pain (13 studies, 1258 participants; Z=1.43, P>0.05).
“We entered 13 studies with 1258 participants into an analysis of the effects of cognitive behavioural therapy (CBT) on pain compared to active control.The overall effect of CBT on pain was not significant (Z = 1.43,P > 0.05) (Analysis 1.1).”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at post-treatment had a just significant effect on catastrophising (6 studies, 735 participants; SMD -0.18, 95% CI -0.36 to 0.00; Z=1.92, P=0.05; I2=31%).
“We entered six studies with 735 participants into an analysis of the effects of CBT on catastrophising; the overall effect of CBT was just significant: Z = 1.92,P = 0.05 (Analysis 1.4).The effect size was SMD -0.18 (95% CI -0.36 to 0.00) and the I value was 31%.”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural therapy compared with active control at post-treatment had a just significant effect on mood (1 study, 71 participants; SMD -0.47, 95% CI -0.94 to 0.00; Z=1.94, P=0.05).
“There was only one study, with 71 participants, in the analysis of the effects of behaviour therapy on mood (Analysis 5.3), with an effect of behaviour therapy that was just significant (Z = 1.94,P = 0.05).The effect size was SMD -0.47 (95% CI -0.94 to 0.00).”
Quote in the paperNot a substantial claim - Findingown data
CBT has a small effect on mood at follow-up compared with doing nothing.
“and a small one at follow-up.”
Quote in the paperSubstantial claim - Findingown data
CBT has a small effect on pain measured immediately post-treatment compared with doing nothing (treatment as usual or waiting list).
“CBT appears to have a small effect on pain measured immediately post-treatment when compared with doing nothing (treatment as usual or waiting list)”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual at post-treatment significantly improved pain (16 studies, 1148 participants; SMD -0.21, 95% CI -0.37 to -0.05; Z=2.59, P<0.05; I2=45%).
“We entered 16 studies with 1148 participants into an analysis of the effects of CBT on pain.The overall effect of CBT was significant (Z = 2.59, P < 0.05) with an effect size of SMD -0.21 (95% CI -0.37 to -0.05) (Analysis 3.1); the I value was 45%.”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural therapy compared with active control at post-treatment had no significant overall effect on disability (2 studies, 110 participants; Z=1.46, P>0.05).
“We entered two studies of 110 participants into an analysis of the effects of behaviour therapy on disability.The overall effect was not significant (Z = 1.46,P > 0.05) (Analysis 5.2).”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual at follow-up had a just significant effect on mood (7 studies, 637 participants; SMD -0.26, 95% CI -0.51 to 0.00; Z=1.99, P=0.05; I2=58%).
“We entered seven studies with 637 patients into an analysis of the effects of CBT on mood at follow-up.The overall effect of CBT was just significant (Z = 1.99,P = 0.05) with a small effect size of SMD -0.26 (95% CI -0.51 to 0.00) (Analysis 4.3); the I value was 58%.”
Quote in the paperSubstantial claim - Findingown data
In the analysis of behaviour therapy versus treatment as usual at follow-up, the overall effect of behaviour therapy on pain was not significant (Z = 0.21, P > 0.05; two studies, 182 participants; Analysis 8.1).
“The overall effect of behaviour therapy was not significant (Z = 0.21, P > 0.05) (Analysis 8.1).”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual at post-treatment significantly improved mood (12 studies, 899 participants; SMD -0.38, 95% CI -0.57 to -0.18; Z=3.84, P<0.01; I2=49%).
“We entered 12 studies with 899 participants into an analysis of the effects of CBT on mood.The overall effect of CBT was significant (Z = 3.84, P < 0.01) (Analysis 3.3).The effect size was SMD -0.38 (95% CI -0.57 to -0.18); the I value was 49%.”
Quote in the paperSubstantial claim - Findingown data
In the analysis of behaviour therapy versus treatment as usual post-treatment, the overall effect of behaviour therapy on pain was not significant (Z = 1.05, P > 0.05; five studies, 484 participants; Analysis 7.1).
“The overall effect of behaviour therapy was not significant (Z = 1.05,P > 0.05) (Analysis 7.1).”
Quote in the paperNot a substantial claim - Findingown data
There were no effects on behaviour therapy effect sizes where there were sufficient data to analyse.
“There were no effects on behaviour therapy effect sizes where there were sufficient data to analyse.”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), there are insufficient studies to meta-analyse behavioural therapy versus active control post-treatment.
“There are insufficient studies in this comparison for meta-analysis.”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual at post-treatment significantly improved catastrophising (5 studies, 308 participants; SMD -0.53, 95% CI -0.76 to -0.31; Z=4.58, P<0.01; I2=0%).
“We entered five studies with 308 participants into an analysis of the effects of CBT on catastrophising.The overall effect of CBT was significant: Z = 4.58, P < 0.01 (Analysis 3.4).The effect size was SMD -0.53 (95% CI -0.76 to -0.31) and the I value was 0%.”
Quote in the paperSubstantial claim - Findingown data
Only one study compared behaviour therapy with active control for mood.
“Behaviour therapy had only one study in which it was compared with active control”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at follow-up had no significant overall effect on catastrophising (2 studies, 282 participants; Z=0.49, P>0.05).
“We entered two studies with 282 participants into an analysis of the effects of CBT on catastrophising.The overall effect of CBT was not significant: Z = 0.49, P > 0.05 (Analysis 2.4).”
Quote in the paperNot a substantial claim - Findingown data
In the analysis of behaviour therapy versus treatment as usual post-treatment, the overall effect of behaviour therapy on catastrophising was just significant (Z = 1.99, P = 0.05; three studies, 269 participants; Analysis 7.4).
“The overall effect was just significant: Z = 1.99,P = 0.05 (Analysis 7.4).”
Quote in the paperNot a substantial claim - Findingown data
CBT has no effect on catastrophising at follow-up compared with active control.
“lost at follow-up”
Quote in the paperNot a substantial claim - Findingown data
Study numbers were too small for behaviour therapy versus active control on catastrophising.
“For behaviour therapy, study numbers were too small in the active control comparison”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at follow-up had no significant overall effect on mood (11 studies, 1261 participants; Z=1.15, P>0.05).
“We entered 11 studies with 1261 participants into an analysis of the effects of CBT on mood at follow-up.The overall effect of CBT was not significant (Z = 1.15,P > 0.05) (Analysis 2.3).”
Quote in the paperNot a substantial claim - Findingown data
Only two studies compared behaviour therapy with an active control for disability.
“although there were only two studies comparing behaviour therapy with an active control.”
Quote in the paperSubstantial claim - Findingown data
In the analysis of behaviour therapy versus treatment as usual post-treatment, the overall effect of behaviour therapy on mood was not significant (Z = 1.18, P > 0.05; three studies, 278 participants; Analysis 7.3).
“The overall effect of behaviour therapy was not significant (Z = 1.18,P > 0.05) (Analysis 7.3).”
Quote in the paperNot a substantial claim - Findingown data
CBT has a moderate effect on catastrophising post-treatment compared with doing nothing.
“but in comparison with doing nothing it had a moderate effect post-treatment”
Quote in the paperSubstantial claim - Findingown data
CBT has no effect on pain immediately post-treatment compared with an active control.
“but not when compared with an active control”
Quote in the paperSubstantial claim - Findingown data
CBT has a small effect on disability at follow-up compared with an active control.
“CBT has a small effect on disability post-treatment and at followup, compared with an active control”
Quote in the paperSubstantial claim - Findingown data
In the analysis of behaviour therapy versus active control at follow-up, the overall effect of behaviour therapy on catastrophising was not significant (Z = 0.25, P > 0.05; one study, 73 participants; Analysis 6.4).
“The overall effect was not significant: Z = 0.25, P > 0.05 (Analysis 6.4).”
Quote in the paperNot a substantial claim - Findingown data
Excluding high risk treatment quality studies raised a small effect size to a moderate one only for mood change for CBT compared to treatment as usual, post-treatment.
“but only in one case did it raise a small effect size to a moderate one: mood change for CBT compared to treatment as usual, post-treatment.”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual at follow-up had no significant overall effect on disability (6 studies, 450 participants; Z=0.66, P>0.05).
“We entered six studies with 450 patients into an analysis of the effects of CBT on disability at follow-up.The overall effect of CBT was not significant (Z = 0.66, P > 0.05) (Analysis 4.2).”
Quote in the paperSubstantial claim - Findingown data
Only one study compared behaviour therapy with an active control for pain.
“there was only one study in the comparison with an active control”
Quote in the paperNot a substantial claim - Findingown data
In the analysis of behaviour therapy versus treatment as usual post-treatment on catastrophising, the effect size was SMD -0.72 (95% CI -1.43 to -0.01).
“The effect size was SMD -0.72 (95% CI -1.43 to -0.01), but the I value was 84%.”
Quote in the paperSubstantial claim - Findingown data
In the analysis of behaviour therapy versus treatment as usual post-treatment, the overall effect of behaviour therapy on disability was not significant (Z = 1.40, P > 0.05; five studies, 504 participants; Analysis 7.2).
“The overall effect was not significant (Z = 1.40,P > 0.05) (Analysis 7.2).”
Quote in the paperNot a substantial claim - Findingown data
In the analysis of behaviour therapy versus treatment as usual at follow-up, the overall effect of behaviour therapy on disability was not significant (Z = 1.08, P > 0.05; three studies, 336 participants; Analysis 8.2).
“the overall effect of behaviour therapy was not significant (Z = 1.08,P > 0.05) (Analysis 8.2).”
Quote in the paperNot a substantial claim - Findingcitation
The size of effects (small to moderate) is similar to other systematic reviews in this field: of mixed chronic pain, low back pain, fibromyalgia and arthritis.
“The size of effects -small to moderate -is similar to other systematic reviews in this field: of mixed chronic pain (Scascighini 2008), low back pain (Henschke 2010a; Hoffman 2007), fibromyalgia (Bernady 2010;Glombiewski 2010;Häuser 2009) and arthritis (Dixon 2007).”
Quote in the paperNot a substantial claim0 of 3 sources checked - Findingown data
No studies provided data on catastrophising at follow-up for the comparison of behaviour therapy versus treatment as usual.
“No studies provided data on catastrophising at follow-up for this comparison.”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural therapy compared with active control at post-treatment had no significant overall effect on pain (1 study, 39 participants; Z=0.77, P>0.05).
“One study of 39 participants was analysed for the effects of behaviour therapy on pain.The overall effect of behaviour therapy was not significant (Z = 0.77, P > 0.05) (Analysis 5.1).”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural therapy compared with active control at post-treatment had no significant overall effect on catastrophising (2 studies, 146 participants; Z=1.67, P>0.05).
“We entered two studies with 146 participants into the analysis of the effects of behaviour therapy on catastrophising.The overall effect was not significant: Z = 1.67,P > 0.05 (Analysis 5.4).”
Quote in the paperNot a substantial claim - Findingown data
Behaviour therapy has no effect on pain compared to doing nothing at either post-treatment or follow-up.
“Behaviour therapy had no effect on pain compared to doing nothing, at either time point”
Quote in the paperSubstantial claim - Findingnone given
Studies of higher quality were already well represented in effect sizes.
“studies of higher quality were already well represented in effect sizes”
Quote in the paperNot a substantial claim - Findingown data
That one study showed no benefit of behaviour therapy for pain post-treatment or at follow-up.
“and that showed no benefit post-treatment or at follow-up.”
Quote in the paperNot a substantial claim - Findingown data
CBT has a small effect on disability post-treatment compared with an active control.
“CBT has a small effect on disability post-treatment and at followup, compared with an active control”
Quote in the paperSubstantial claim - Findingcitation
An analysis of quality scores, as measured by the Yates et al scale, showed that the quality of the design and reporting of trials has clearly improved over the years.
“An analysis of quality scores, as measured by the Yates et al scale (Yates 2005), showed that the quality of the design and reporting of trials has clearly improved over the years”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Yates 2005 source
Not checked in the free run.
- Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual at follow-up had no significant overall effect on catastrophising (1 study, 59 participants; Z=0.84, P>0.05).
“There was only one study of 59 participants in the analysis of the effects of CBT on catastrophising.The overall effect of CBT was not significant: Z = 0.84, P > 0.05 (Analysis 4.4).”
Quote in the paperNot a substantial claim - Findingown data
Behaviour therapy has no effect on disability compared to doing nothing post-treatment or at follow-up.
“Behaviour therapy had no effect on disability compared to active control or to doing nothing, post-treatment or at follow-up”
Quote in the paperSubstantial claim - Findingown data
Behaviour therapy has no effect on disability compared to active control post-treatment or at follow-up.
“Behaviour therapy had no effect on disability compared to active control or to doing nothing, post-treatment or at follow-up”
Quote in the paperSubstantial claim - Findingown data
CBT has a small effect on catastrophising immediately post-treatment compared with active control.
“CBT had a small effect compared to active control immediately post-treatment”
Quote in the paperSubstantial claim - Findingown data
Behaviour therapy showed no effect on mood at follow-up compared with doing nothing.
“behaviour therapy showed no effect either post-treatment or at follow-up compared with doing nothing (treatment as usual or waiting list).”
Quote in the paperNot a substantial claim - Findingown data
Behaviour therapy showed no effect on mood post-treatment compared with doing nothing.
“behaviour therapy showed no effect either post-treatment or at follow-up compared with doing nothing (treatment as usual or waiting list).”
Quote in the paperNot a substantial claim - Findingown data
In the analysis of behaviour therapy versus treatment as usual post-treatment on catastrophising, heterogeneity was high (I = 84%).
“but the I value was 84%.”
Quote in the paperNot a substantial claim - Findingown data
There were no follow-up data for behaviour therapy versus doing nothing on catastrophising.
“there were no follow-up data.”
Quote in the paperNot a substantial claim - Findingnone given
CBT has no effect on mood immediately post-treatment compared with active control.
“CBT has no effect on mood immediately post-treatment compared with active control”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual at follow-up had no significant overall effect on pain (7 studies, 635 participants; Z=0.99, P>0.05).
“We entered seven studies with 635 participants into an analysis of the effects of CBT on pain at follow-up.The overall effect of CBT was not significant (Z = 0.99, P > 0.05) (Analysis 4.1).”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual at post-treatment significantly improved disability (15 studies, 1105 participants; SMD -0.26, 95% CI -0.47 to -0.04; Z=2.35, P<0.05; I2=67%).
“We entered 15 studies with 1105 participants into an analysis of the effects of CBT on disability.The overall effect was significant (Z = 2.35, P < 0.05) (Analysis 3.2).The effect size was SMD -0.26 (95% CI -0.47 to -0.04); the I value was 67%.”
Quote in the paperSubstantial claim - Findingreasoning
CBT has no effect on disability at follow-up compared with doing nothing.
“but this effect disappeared at follow-up.”
Quote in the paperNot a substantial claim - Findingown data
CBT has a moderate effect on mood immediately post-treatment compared with doing nothing (treatment as usual or waiting list).
“when compared with doing nothing (treatment as usual or waiting list), it has a moderate effect size immediately post-treatment”
Quote in the paperSubstantial claim - Findingown data
There are insufficient studies in the comparison of behaviour therapy versus active control at follow-up for meta-analysis.
“There are insufficient studies in this comparison for meta-analysis.”
Quote in the paperSubstantial claim - Findingown data
Treatment quality was not associated with post-treatment N (rho = 0.17, P > 0.1).
“although treatment quality was not associated with post-treatment N (rho = 0.17, P > 0.1)”
Quote in the paperNot a substantial claim - Findingown data
CBT has no effect on pain at follow-up.
“and there is no effect at follow-up.”
Quote in the paperSubstantial claim - Findingown data
CBT has a small effect on disability post-treatment compared with doing nothing.
“and post-treatment compared with doing nothing”
Quote in the paperSubstantial claim - Findingown data
In the analysis of behaviour therapy versus active control at follow-up, the overall effect of behaviour therapy on disability was not significant (Z = 1.01, P > 0.05; two studies, 144 participants; Analysis 6.2).
“The overall effect of behaviour therapy was not significant (Z = 1.01,P > 0.05) (Analysis 6.2).”
Quote in the paperNot a substantial claim - Findingown data
Data from 35 randomised controlled trials (4788 treated participants) of specific behavioural or cognitive behavioural therapy were used.
“we were able to use data from 35 randomised controlled trials (RCTs) (4788 treated participants) of specific behavioural or cognitive behavioural therapy.”
Quote in the paperSubstantial claim - Findingown data
There is a large evidence base for estimating the effectiveness of psychological treatments in chronic pain.
“There is a large evidence base for estimating the effectiveness of psychological treatments in chronic pain.”
Quote in the paperSubstantial claim - Findingown data
Behaviour therapy has a small effect on catastrophising immediately post-treatment compared with doing nothing.
“in comparison with doing nothing, behaviour therapy had a small effect immediately post-treatment”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural treatment compared with treatment as usual at follow-up showed no statistically significant difference in pain (SMD -0.03, 95% CI -0.32 to 0.26).
“Total *** 94 88 100% -0.03[-0.32,0.26]Heterogeneity: Tau =0; Chi =0.02, df=1(P=0.89);I =0% Test for overall effect: Z=0.21(P=0.83)”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), cognitive behavioural therapy compared with treatment as usual or waitlist at follow-up showed no statistically significant difference in disability (SMD -0.13, 95% CI -0.51 to 0.25).
“Total *** 218 232 100% -0.13[-0.51,0.25]Heterogeneity: Tau =0.16; Chi =19.43, df=5(P=0); I =74.27%Test for overall effect: Z=0.66(P=0.51)”
Quote in the paperSubstantial claim - Findingnone given
The evidence for behaviour therapy is weak or lacking.
“The evidence for behaviour therapy is weak or lacking.”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural treatment compared with treatment as usual at follow-up showed no statistically significant difference in disability (SMD -0.54, 95% CI -1.51 to 0.44).
“Total *** 172 164 100% -0.54[-1.51,0.44]Heterogeneity: Tau =0.69; Chi =33.37, df=2(P<0.0001);I =94.01%Test for overall effect: Z=1.08(P=0.28)”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), cognitive behavioural therapy compared with treatment as usual or waitlist at follow-up showed no statistically significant difference in pain (SMD -0.09, 95% CI -0.25 to 0.08).
“Total *** 310 325 100% -0.09[-0.25,0.08]Heterogeneity: Tau =0.01; Chi =6.71, df=6(P=0.35);I =10.61%Test for overall effect: Z=0.99(P=0.32)”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at post-treatment reduces disability (SMD -0.19, 95% CI -0.33 to -0.05; 12 studies, 1130 participants).
“2 Disability 12 1130 Std.Mean Difference (IV, Random, 95% CI) -0.19 [-0.33, -0.05]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), cognitive behavioural therapy (CBT) compared with active control at post-treatment does not significantly reduce pain (SMD -0.10, 95% CI -0.24 to 0.04; 13 studies, 1258 participants).
“1 Pain 13 1258 Std.Mean Difference (IV, Random, 95% CI) -0.10 [-0.24, 0.04]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural treatment compared with treatment as usual post-treatment showed no statistically significant difference in disability (SMD -0.41, 95% CI -0.98 to 0.16).
“Total *** 266 238 100% -0.41[-0.98,0.16]Heterogeneity: Tau =0.36; Chi =36.39, df=4(P<0.0001);I =89.01%Test for overall effect: Z=1.4(P=0.16)”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural treatment compared with treatment as usual post-treatment showed a statistically significant reduction in catastrophising (SMD -0.72, 95% CI -1.43 to -0.01).
“Total *** 146 123 100% -0.72[-1.43,-0.01]Heterogeneity: Tau =0.33; Chi =12.73, df=2(P=0); I =84.29%Test for overall effect: Z=1.99(P=0.05)”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural treatment compared with treatment as usual at follow-up showed no statistically significant difference in mood (SMD -0.65, 95% CI -2.07 to 0.77).
“Total *** 83 77 100% -0.65[-2.07,0.77]Heterogeneity: Tau =0.99; Chi =16.68, df=1(P<0.0001);I =94% Test for overall effect: Z=0.9(P=0.37)”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual reduces mood symptoms (SMD -0.38, 95% CI -0.57 to -0.18; 12 studies, 899 participants).
“3 Mood 12 899 Std.Mean Difference (IV, Random, 95% CI) -0.38 [-0.57, -0.18]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at follow-up does not significantly reduce pain (SMD -0.08, 95% CI -0.23 to 0.06; 11 studies, 1261 participants).
“1 Pain 11 1261 Std.Mean Difference (IV, Random, 95% CI) -0.08 [-0.23, 0.06]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural treatment compared with active control post-treatment showed no statistically significant difference in disability (SMD -0.26, 95% CI -0.58 to 0.07).
“Total *** 77 71 100% -0.26[-0.58,0.07]Heterogeneity: Tau =0; Chi =0, df=1(P=0.95);I =0% Test for overall effect: Z=1.56(P=0.12)”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual reduces pain (SMD -0.21, 95% CI -0.37 to -0.05; 16 studies, 1148 participants).
“1 Pain 16 1148 Std.Mean Difference (IV, Random, 95% CI) -0.21 [-0.37, -0.05]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at post-treatment does not significantly reduce mood symptoms (SMD -0.05, 95% CI -0.19 to 0.09; 13 studies, 1256 participants).
“3 Mood 13 1256 Std.Mean Difference (IV, Random, 95% CI) -0.05 [-0.19, 0.09]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual at follow-up reduces mood symptoms (SMD -0.26, 95% CI -0.51 to -0.00; 7 studies, 637 participants).
“3 Mood 7 637 Std.Mean Difference (IV, Random, 95% CI) -0.26 [-0.51, -0.00]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at follow-up does not significantly reduce mood symptoms (SMD -0.07, 95% CI -0.18 to 0.05; 11 studies, 1261 participants).
“3 Mood 11 1261 Std.Mean Difference (IV, Random, 95% CI) -0.07 [-0.18, 0.05]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual at follow-up does not significantly reduce disability (SMD -0.13, 95% CI -0.51 to 0.25; 6 studies, 450 participants).
“2 Disability 6 450 Std.Mean Difference (IV, Random, 95% CI) -0.13 [-0.51, 0.25]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual reduces disability (SMD -0.26, 95% CI -0.47 to -0.04; 15 studies, 1105 participants).
“2 Disability 15 1105 Std.Mean Difference (IV, Random, 95% CI) -0.26 [-0.47, -0.04]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual at follow-up does not significantly reduce pain (SMD -0.09, 95% CI -0.25 to 0.08; 7 studies, 635 participants).
“1 Pain 7 635 Std.Mean Difference (IV, Random, 95% CI) -0.09 [-0.25, 0.08]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at post-treatment does not significantly reduce catastrophising (SMD -0.18, 95% CI -0.36 to 0.00; 6 studies, 735 participants).
“4 Catastrophising 6 735 Std.Mean Difference (IV, Random, 95% CI) -0.18 [-0.36, 0.00]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with treatment as usual reduces catastrophising (SMD -0.53, 95% CI -0.76 to -0.31; 5 studies, 308 participants).
“4 Catastrophising 5 308 Std.Mean Difference (IV, Random, 95% CI) -0.53 [-0.76, -0.31]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural treatment compared with treatment as usual post-treatment showed no statistically significant difference in mood (SMD -0.53, 95% CI -1.42 to 0.35).
“Total *** 150 128 100% -0.53[-1.42,0.35]Heterogeneity: Tau =0.55; Chi =24.13, df=2(P<0.0001);I =91.71%”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at follow-up reduces disability (SMD -0.15, 95% CI -0.28 to -0.02; 12 studies, 1295 participants).
“2 Disability 12 1295 Std.Mean Difference (IV, Random, 95% CI) -0.15 [-0.28, -0.02]”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), CBT compared with active control at follow-up does not significantly reduce catastrophising (SMD 0.06, 95% CI -0.18 to 0.29; 2 studies, 282 participants).
“4 Catastrophising 2 282 Std.Mean Difference (IV, Random, 95% CI) 0.06 [-0.18, 0.29]”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural treatment compared with active control post-treatment showed no statistically significant difference in catastrophising (SMD -0.28, 95% CI -0.60 to 0.05).
“Total *** 76 70 100% -0.28[-0.6,0.05]Heterogeneity: Tau =0; Chi =0.14, df=1(P=0.71);I =0% Test for overall effect: Z=1.67(P=0.1)”
Quote in the paperNot a substantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural treatment compared with active control at follow-up showed no statistically significant difference in disability (SMD -0.17, 95% CI -0.50 to 0.16).
“Total *** 74 70 100% -0.17[-0.5,0.16]Heterogeneity: Tau =0; Chi =0.03, df=1(P=0.87);I =0% Test for overall effect: Z=1.01(P=0.31)”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), behavioural treatment compared with treatment as usual post-treatment showed no statistically significant difference in pain (SMD -0.27, 95% CI -0.79 to 0.24).
“Total *** 254 230 100% -0.27[-0.79,0.24]Heterogeneity: Tau =0.29; Chi =29.36, df=4(P<0.0001);I =86.38%Test for overall effect: Z=1.05(P=0.29)”
Quote in the paperSubstantial claim - Findingown data
In adults with chronic pain (excluding headache), cognitive behavioural therapy compared with treatment as usual or waitlist at follow-up showed a statistically significant reduction in mood symptoms (SMD -0.26, 95% CI -0.51 to 0.00).
“Total *** 312 325 100% -0.26[-0.51,-0]Heterogeneity: Tau =0.07; Chi =14.26, df=6(P=0.03);I =57.92%Test for overall effect: Z=1.99(P=0.05)”
Quote in the paperSubstantial claim - Interpretationreasoning
Most judgements of high risk of bias were because of inadequate reporting.
“Thus most judgements of high risk of bias were because of inadequate reporting: we recognise that this is a conservative position and that some studies may have exercised proper precautions in some or all of these areas.”
Quote in the paperNot a substantial claim - Interpretationnone given
The results cannot be extrapolated to CBT delivered by untrained staff.
“The results cannot be extrapolated to CBT delivered by untrained staff.”
Quote in the paperSubstantial claim - Study design and conductown data
In the Basler 1997 trial, random sequence generation was at high risk of bias.
““Through assignment of random numbers, patients were allocated to an experimental treatment or a control group.””
Quote in the paperNot a substantial claim - Interpretationnone given
CBT is effective when delivered by experienced staff, those trained and supervised in the trial protocol, or both.
“CBT is effective when delivered by experienced staff, those trained and supervised in the trial protocol, or both.”
Quote in the paperSubstantial claim - Study design and conductown data
In the Alaranta 1994 trial, incomplete outcome data was at high risk of bias.
“Attrition implied not reported; no reporting of differences”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Buckelew 1998 trial, incomplete outcome data was at unclear risk of bias.
“Attrition partially reported and did not differ across groups; no test for differences”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Bliokas 2007 trial, blinding of outcome assessment was at high risk of bias.
“Examination by physiotherapist and self report: no blinding reported”
Quote in the paperNot a substantial claim - Study design and conductown data
In the De Souza 2008 trial, incomplete outcome data was at high risk of bias.
“Attrition partially reported; no test for differences”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Basler 1997 trial, incomplete outcome data was at low risk of bias.
“Attrition reported; 1 difference found between dropouts and completers”
Quote in the paperNot a substantial claim - Study design and conductreasoning
In the Alaranta 1994 trial, allocation concealment was at high risk of bias.
“No information but post-randomisation exclusion of patients “not fit” for intervention group”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Buckelew 1998 trial, blinding of outcome assessment was at low risk of bias.
“Subjects examined by physician unaware of treatment conditions and with no other contact with subjects”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Alaranta 1994 trial, selective reporting was at high risk of bias.
“Many outcomes not reported”
Quote in the paperNot a substantial claim - Interpretationnone given
Average effects mask larger changes on the part of some patients and little or none for others.
“Average effects mask larger changes on the part of some patients and little or none for others.”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Altmaier 1992 trial, random sequence generation was at high risk of bias.
“Abstract: “Forty-five low back pain patients were randomly assigned”; no details in Methods”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Altmaier 1992 trial, incomplete outcome data was at high risk of bias.
“Inadequately reported”
Quote in the paperNot a substantial claim - Study design and conductreasoning
In the Buckelew 1998 trial, random sequence generation was at high risk of bias.
““randomly assigned””
Quote in the paperNot a substantial claim - Study design and conductreasoning
In the Alaranta 1994 trial, random sequence generation was at high risk of bias.
“patients stratified according to age … and sex and randomly divided into intervention and control groups”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Alaranta 1994 trial, blinding of outcome assessment was at high risk of bias.
“Self report and examination by physiatrist and physiotherapist at baseline and follow-up.No statement about blinding.”
Quote in the paperNot a substantial claim - Premisecitation
Poorer quality trials tend to produce more positive results.
“the overall tendency for poorer quality trials to produce more positive results (Furlan 2001;Ioannidis 2005;Nuesch 2009).”
Quote in the paperSubstantial claim0 of 3 sources checked - Study design and conductown data
In the Greco 2004 trial, blinding of outcome assessment was at low risk of bias.
“Rheumatologist and researcher assessors masked to treatment assignment”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Geraets 2005 trial, incomplete outcome data was at low risk of bias.
“Attrition fully reported; dropouts different in pain characteristics but not outcome measures at baseline”
Quote in the paperNot a substantial claim - Study design and conductreasoning
In the Greco 2004 trial, allocation concealment was at high risk of bias.
“Not reported, but equal credibility of treatments rated by participants”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Haldorsen 1998 trial, selective reporting was at high risk of bias.
“Not fully reported”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Haldorsen 1998 trial, incomplete outcome data was at high risk of bias.
“Attrition partially reported; no test for differences”
Quote in the paperNot a substantial claim - Study design and conductown data
In the Geraets 2005 trial, allocation concealment was at low risk of bias.
“Random number table generated by person not involved in study; opaque sealed envelopes; “Blinding for patients .... of allocated treatment was not possible” but treatment preferences elicited and shown to have no effect on outcome”
Quote in the paperNot a substantial claim - Study design and conductreasoning
In the Haldorsen 1998 trial, allocation concealment was at low risk of bias.
“Allocation sequence by someone not involved in study”
Quote in the paperNot a substantial claim - Premisecitation
Small numbers are associated with bias.
“given the demonstrated association between small numbers and bias (Ioannidis 2005; Moore 2010; Nuesch 2009).”
Quote in the paperSubstantial claim0 of 3 sources checked
- May combine two claims. 47
- Classified as probably not a substantial claim. 168
- The quote only partly states this claim. 4
May combine two claims.
Findingown dataThe mean quality of treatment was 5.4/9 (SD 2.3) and was unrelated to year of publication.
“The mean quality of treatment was 5. 4/9 (SD 2.3, range 1 to 9) and was unrelated to year of publication (Spearman's rho = 0.20, nonsignificant).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataOf the 24 analyses reported, 10 showed low heterogeneity, six showed modest heterogeneity, and eight showed large heterogeneity.
“Of the 24 analyses reported (CBT or behaviour therapy versus active control or treatment as usual, post-treatment and follow-up, for 'pain', 'disability', 'mood' and 'catastrophic thinking'), 10 showed low heterogeneity (I < 25%), six showed modest heterogeneity (I > 25% to < 50%) and eight, almost all analyses of behaviour therapy, showed large heterogeneity (I > = 50%).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe mean quality of trial design was 15.8/26 (SD 4.3) and increased with year of publication (Spearman's rho = 0.41, P < 0.01).
“As in the 2009 systematic review, we scored the quality of trial design and found a mean 15.8/26 (standard deviation (SD) 4.3, range 9 to 24/26) which increased with year of publication (Spearman's rho = 0.41, P < 0.01); this represented an improvement of about two points per decade.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataN at the end of treatment was associated with design quality score and with total quality score.
“N at the end of treatment was associated with design quality score and with total quality score (rho = 0.41 (P < 0.01) and 0.38 respectively (P < 0.05)).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenTreatment quality was not associated with year of study.
“Treatment quality was not associated with year of study: see Included studies.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThis review includes 22 trials from the previous systematic review and 20 new or re-entered trials; seven trials provided no useable data.
“This review includes 22 trials from the previous systematic review and 20 new or re-entered trials; seven trials provided no useable”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataOf the eight comparisons of CBT versus active control, three were positive: disability immediately post-treatment and at follow-up, and catastrophic thinking post-treatment.
“Of the eight comparisons of CBT versus active control (four outcomes: pain, disability, mood, catastrophic thinking, at two time points, immediately post-treatment and six to 12 months followup), three were positive: disability immediately post-treatment and at follow-up, and catastrophic thinking post-treatment.”
Quote in the paperSubstantial claimThe quote only partly states this claim.
Findingown dataIn the analysis of behaviour therapy versus treatment as usual at follow-up, the overall effect of behaviour therapy on mood was not significant (Z = 0.90, P > 0.05; two studies, 160 participants; Analysis 8.3).
“The overall effect of behaviour therapy was not significant (Z = 0.90, P > 0.05) (Analysis 8.3).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataBefore applying the new sample size criterion, 65 eligible trials were found.
“Before applying our new sample size criterion, we found 65 eligible trials”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataCBT and behaviour therapy dominate the evidence base; there were no trials of other psychological treatments such as psychodynamic or interpersonal psychotherapy, or dialectical behaviour therapy.
“Cognitive behavioural therapy (CBT) and behaviour therapy dominate the evidence base; there were no trials of other psychological treatments such as psychodynamic or interpersonal psychotherapy, or dialectical behaviour therapy.”
Quote in the paperSubstantial claimThe quote only partly states this claim.
Findingown dataIn the analysis of behaviour therapy versus active control at follow-up, the overall effect of behaviour therapy on pain was not significant (Z = 0.13, P > 0.05; one study, 73 participants; Analysis 6.1).
“The overall effect of behaviour therapy was not significant (Z = 0.13, P > 0.05) (Analysis 6.1).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataIn Analysis 4.3, removal of Van Koulil 2010 reduced heterogeneity to 9% but produced a non-significant result in place of the just significant one (Z = 1.57, P > 0.05).
“and reduced it to 9% (Analysis 4.3) but also produced a non-significant result in place of the just significant one: Z was 1.57, P > 0.05.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Van Koulil 2010 source
Not checked in the free run.
May combine two claims.
Findingnone givenThe remainder allowed for reasonable power in the analyses, with the largest analysis being of 1258 participants (CBT versus active control post-treatment) and the smallest of 144 participants (behaviour therapy versus active control at follow-up).
“The remainder allowed for reasonable power in the analyses, with the largest analysis being of 1258 participants (CBT versus active control post-treatment) and the smallest of 144 participants (behaviour therapy versus active control at follow-up).”
Quote in the paperNot a substantial claimMay combine two claims.
FindingreasoningFor behaviour therapy, the evidence is much weaker and, with more stringent criteria, rather sparse.
“For behaviour therapy the evidence is much weaker and, with our more stringent criteria, rather sparse.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingnone givenThe majority of studies were of CBT, reflecting its dominance in chronic pain management and in psychological treatment more widely.
“The majority of studies were of CBT, reflecting its dominance in chronic pain management and in psychological treatment more widely.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataIn Analysis 3.2, heterogeneity was reduced to 55% by removal of one positive outlier (Williams 1996), without affecting the overall significant result.
“In Analysis 3.2, heterogeneity was reduced to 55% by the removal of one positive outlier (Williams 1996), without affecting the overall significant result.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Williams 1996 source
Not checked in the free run.
May combine two claims.
Findingown dataThe quality of treatments, of their reporting, or both, does not appear to have improved over time.
“However, the quality of treatments, of their reporting, or both, does not appear to have improved over time”
Quote in the paperNot a substantial claimThe quote only partly states this claim.
Findingown dataCBT has a moderate effect on catastrophising at follow-up compared with doing nothing (sustained).
“which was sustained at follow-up.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataIn Analysis 7.4, removal of Thieme 2003 reduced heterogeneity to 0% and strengthened the result (Z = 2.41, P < 0.05; SMD -0.34, 95% CI -0.62 to -0.06), now based on two studies.
“In Analysis 7.4, again removal of a single study (Thieme 2003) reduced heterogeneity to 0% and strengthened the result, although this was now only produced by two studies: Z = 2.41 P < 0.05; the effect size was SMD -0.34 (95% CI -0.62 to -0.06).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Thieme 2003 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
FindingcitationThe Yates 2005 treatment subscale is restricted to five items and may be relatively insensitive.
“but the Yates 2005 treatment subscale is restricted to five items so may be relatively insensitive.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Yates 2005 source
Not checked in the free run.
May combine two claims.
Findingown dataExcluding studies classified as 'high risk' for treatment quality largely increased CBT effect sizes and reduced heterogeneity.
“This largely had the effect of increasing CBT effect sizes and reducing heterogeneity”
Quote in the paperNot a substantial claimThe quote only partly states this claim.
Findingown dataIn the analysis of behaviour therapy versus active control at follow-up, the overall effect of behaviour therapy on mood was not significant (Z = 1.55, P > 0.05; one study, 71 participants; Analysis 6.3).
“The overall effect of behaviour therapy was not significant (Z = 1.55,P > 0.05) (Analysis 6.3).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataIn Analysis 4.2, removal of a single study (Van Koulil 2010) reduced heterogeneity to 0% without changing the non-significant result.
“In Analysis 4.2 and Analysis 4.3, removal of a single study (Van Koulil 2010) reduced heterogeneity to 0% but without changing the non-significant result (Analysis 4.2)”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Van Koulil 2010 source
Not checked in the free run.
May combine two claims.
Findingown dataOf the four outcome domains, effects on mood (mostly depression) were strongest, followed by catastrophic thinking, disability and, lastly, pain.
“Of our four outcome domains, effects on mood (mostly depression) were strongest, followed by catastrophic thinking, disability and, lastly, pain.”
Quote in the paperSubstantial claimMay combine two claims.
Findingnone givenCompared to the 2009 review, the effect sizes for CBT are largely sustained and extended with the addition of catastrophic thinking as an outcome, while those for behaviour therapy are diminished.
“Compared to our 2009 review (Eccleston 2009a), the effect sizes for CBT are largely sustained and extended with the addition of catastrophic thinking as an outcome, while those for behaviour therapy are diminished.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Eccleston 2009a
Not checked in the free run.
May combine two claims.
Findingnone givenNumbers in trials have steadily increased over time, but in some cases this appears to be at the cost of treatment intensity.
“Numbers in trials have steadily increased over time, but in some cases this appears to be at the cost of treatment intensity”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationThe effect sizes are comparable with effect sizes of CBT for pain problems in children and for major psychological disorders.
“It is also comparable with effect sizes of CBT for pain problems in children (Eccleston 2009b) and for major psychological disorders (Butler 2006).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Eccleston 2009b
Not checked in the free run.
- cites Butler 2006 source
Not checked in the free run.
May combine two claims.
FindingcitationTreatment gains are of the same order as those of other available treatments, as shown by head-to-head trials of surgery versus psychologically based rehabilitation.
“Treatment gains are of the same order as those of other available treatments (Glombiewski 2010), as shown by head-to-head trials of surgery versus psychologically based rehabilitation (Fairbank 2005;Hellum 2011).”
Quote in the paperSubstantial claim0 of 3 sources checkedMay combine two claims.
FindingcitationThe average effects are small, as they are for all treatments of chronic pain.
“The average effects are small, as they are for all treatments of chronic pain (Moore 2010).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Moore 2010 source
Not checked in the free run.
May combine two claims.
Findingnone givenNo data were available in the trials on adverse events, withdrawal and escape or emergency analgesia.
“No data were available in the trials on adverse events, withdrawal and escape or emergency analgesia.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingnone givenThe evidence for CBT is stronger, particularly when compared with treatment as usual/waiting list, and for mood and catastrophic thinking.
“The evidence for CBT is stronger, particularly when compared with treatment as usual/waiting list, and for mood and catastrophic thinking.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing). May combine two claims.
PremisecitationOther developments in psychological science have led to new forms of treatments being promoted, and the quality of trials and trial reporting is thought to be improving.
“Other developments in psychological science have led to new forms of treatments being promoted, and the quality of trials and trial reporting is thought to be improving (Morley 2006).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Morley 2006 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationWe applied a quality rating scale specifically designed for psychological interventions in pain.
“As in the previous review (Eccleston 2009a), we applied a quality rating scale specifically designed for psychological interventions in pain (Yates 2005).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Yates 2005 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationBehavioural and cognitive treatments designed to ameliorate pain, distress and disability were first introduced over 40 years ago and are now well established.
“Behavioural and cognitive treatments designed to ameliorate pain, distress and disability were first introduced over 40 years ago and are now well established (Fordyce 1968; Keefe Rumble 2004).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Fordyce 1968 source
Not checked in the free run.
- cites Keefe Rumble 2004
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataTwo of the three review authors scored all studies and reached a consensus after initial comparison of ratings.
“Two of the three review authors scored all studies and they reached a consensus a er initial comparison or ratings.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown data14 studies had adequate allocation concealment, one uncertain, and 27 high risk.
“We judged 14 studies to have adequate allocation concealment, one uncertain and 27 high risk, again mainly because there was no description of any procedure designed to do so.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationThe Eccleston 2009a review found 52 trials, of which 40 had data that could be entered into a meta-analysis.
“The Eccleston 2009a review found 52 trials, of which 40 had data that could be entered into a meta-analysis.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Eccleston 2009a
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductreasoningWe excluded the option of 'blinding participants and personnel' because neither therapists nor patients can be blinded to whether they deliver or receive treatment.
“We excluded the option of 'blinding participants and personnel' because neither therapists nor patients can be blinded to whether they deliver or receive treatment.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductown dataFifteen studies described a convincing method of randomisation and were judged low risk of bias; 11 provided an inadequate description and were judged unclear.
“Fi een studies described a convincing method of randomisation so we judged them to have a low risk of bias, and a further 11 provide an inadequate description so we judged them to be unclear.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable). May combine two claims.
PremisecitationThis analysis is now out of date and in need of updating.
“This analysis is now out of date and in need of updating (Shojania 2007).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Shojania 2007 source
Not checked in the free run.
May combine two claims.
Study design and conductown data13 studies were judged low risk of bias for outcome assessment (blinded assessors); two unclear; 27 high risk.
“Finally, we judged 13 studies at low risk of bias for outcome assessment since they used blinded assessors; two were unclear; and we judged 27 at high risk of bias since they gave no details of outcome assessment procedures.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductcitationWe required N > 20 per treatment arm at post-treatment assessment because of the recognised risk of bias of small numbers.
“This last criterion of N > 20 at post-treatment assessment is an improvement from the Eccleston 2009a review in which we used an entry of N > 10.We made this change because of the recognised risk of bias of small numbers (Ioannidis 2005;Nuesch 2009); raising the required N further would be desirable but would exclude too many studies.”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
Study design and conductown data34 studies were judged low risk of bias for selective reporting; one uncertain; seven high risk.
“We judged 34 studies at low risk of bias for selective reporting of outcome since they reported all outcomes, or in one case accounted for those they did not report; we judged one study uncertain because outcomes were combined in factor scores, and seven studies did not report all outcomes which they described in assessment sections of their Methods, and we judged them at high risk of bias.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationCompared with doing nothing, behaviour therapy improved pain post-treatment, but showed no other benefits, and there were too few trials of behaviour therapy against active control for analysis.
“Compared with doing nothing, behaviour therapy improved pain post-treatment, but showed no other benefits, and there were too few trials of behaviour therapy against active control for analysis.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Eccleston 2009a
Not checked in the free run.
May combine two claims.
PremisecitationAgainst doing nothing (treatment as usual or waiting list control), there was only significant improvement for pain post-treatment and mood at follow-up.
“Surprisingly, against doing nothing (treatment as usual or waiting list control), there was only significant improvement for pain post-treatment and mood at follow-up.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Eccleston 2009a
Not checked in the free run.
May combine two claims.
Study design and conductown data16 studies were judged high risk of bias for randomisation, mainly because the method of randomisation was not described.
“We judged 16 to have high risk of bias, mainly because the method of randomisation was not described; these were mainly earlier studies.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationAgainst active control, CBT improved disability post-treatment, and pain, disability and mood at follow-up, although effect sizes were small.
“Against active control, CBT improved disability post-treatment, and pain, disability and mood at follow-up, although effect sizes were small.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Eccleston 2009a
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataMean study completion rate from entry to post-treatment assessment was 87.6% (SD 9.5%).
“Mean study completion rate from entry to posttreatment assessment was 87.6% (SD 9.5%) and ranged from 65% to 100%.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductcitationWe assessed risk of bias using the recommended Cochrane guidance.
“We assessed risk of bias using the recommended Cochrane guidance (Higgins 2011).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Higgins 2011
Not checked in the free run.
May combine two claims.
InterpretationreasoningTrials of behaviour therapy tended to be small and methodologically weak and have been largely superseded by procedures that claim to be cognitive behavioural.
“As a consequence, trials tended to be small and methodologically weak and have been largely superseded by procedures that claim to be cognitive behavioural.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationBehaviour therapy was developed in the 1960s and 1970s and evaluated as part of the first wave of psychological treatment for pain.
“Behaviour therapy was developed in the 1960s and 1970s and evaluated as part of the first wave of psychological treatment for pain (Morley 2011).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Morley 2011 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn the Evers 2002 trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Ersek 2008 trial, random sequence generation was at low risk of bias.
“Randomisation by (retirement) facility, by statistician using random number generator”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn the Ehrenborg 2010 trial, blinding of outcome assessment was at high risk of bias.
“Therapists conducted assessments: statement that study not blinded”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataThe evidence of weak to moderate effects across a range of outcomes is clear from our systematic reviews and from the others cited above, and is very unlikely to change as a result of further similar RCTs and systematic reviews.
“The evidence of weak to moderate effects across a range of outcomes is clear from our systematic reviews and from the others cited above, and is very unlikely to change as a result of further similar RCTs and systematic reviews.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductnone givenIn the Evers 2002 trial, blinding of outcome assessment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
Interpretationnone givenIt is no longer believed possible to design a 'pure' trial of a single component of intervention (such as relaxation, operant reinforcement or acceptance).
“We no longer believe that it is possible to design a 'pure' trial of a single component of intervention (such as relaxation, operant reinforcement or acceptance)”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn the Evers 2002 trial, allocation concealment was at low risk of bias.
““previously determined””
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductnone givenIn the Bliokas 2007 trial, allocation concealment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductnone givenIn the Altmaier 1992 trial, blinding of outcome assessment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductreasoningIn the De Souza 2008 trial, allocation concealment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn the Evers 2002 trial, incomplete outcome data was at low risk of bias.
“Attrition fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Ersek 2008 trial, allocation concealment was at low risk of bias.
“By independent statistician”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductreasoningIn the Altmaier 1992 trial, allocation concealment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationAlthough trials do not tend to report adverse effects or deterioration, such effects should be small, so the treatment can be considered to be safe, with the reservation that reasons for discontinuing treatment are rarely given and may be due to hidden adverse effects.
“Although trials do not tend to report adverse effects or deterioration (such as worsening of depression to a level of clinical concern), we know that such effects should be small (Fairbank 2005;Hellum 2011;Morley 2008), so the treatment can be considered to be safe, with the reservation that the reasons for discontinuing treatment are rarely given and may be due to hidden adverse effects.”
Quote in the paperSubstantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn the Evers 2002 trial, random sequence generation was at unclear risk of bias.
“Random numbers”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationnone givenPsychological interventions can reduce pain, disability, psychological distress and catastrophic ways of thinking about pain.
“Psychological interventions can reduce pain, disability, psychological distress and catastrophic ways of thinking about pain.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn the Ersek 2008 trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn the Falcao 2008 trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Altmaier 1992 trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Falcao 2008 trial, incomplete outcome data was at unclear risk of bias.
“Attrition partially reported; statement that dropouts were not different”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn the Buckelew 1998 trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Bliokas 2007 trial, incomplete outcome data was at low risk of bias.
“Attrition fully reported; no differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductreasoningIn the Buckelew 1998 trial, allocation concealment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Falcao 2008 trial, random sequence generation was at unclear risk of bias.
““Patients were randomized by drawing lots””
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductreasoningIn the Falcao 2008 trial, allocation concealment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn the Ersek 2008 trial, blinding of outcome assessment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Ehrenborg 2010 trial, incomplete outcome data was at low risk of bias.
“Attrition fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductreasoningIn the Ehrenborg 2010 trial, allocation concealment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningThere is no clear benefit of adding further components to multicomponent CBT; it is unlikely that the extra component, such as two sessions on 'mindfulness', will make any measurable difference.
“There is no clear benefit of adding further components to multicomponent CBT: it is unlikely that the extra component, such as two sessions on 'mindfulness', will make any measurable difference.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn the Bliokas 2007 trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn the Basler 1997 trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Ehrenborg 2010 trial, random sequence generation was at unclear risk of bias.
““Randomization was performed by casting a die after the participant's acceptance: odd numbers for treatment group ....””
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductnone givenIn the De Souza 2008 trial, blinding of outcome assessment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn the De Souza 2008 trial, random sequence generation was at high risk of bias.
““randomly assigned””
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductreasoningIn the Basler 1997 trial, allocation concealment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn the Ehrenborg 2010 trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Bliokas 2007 trial, random sequence generation was at low risk of bias.
“Random numbers generation”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn the De Souza 2008 trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Ersek 2008 trial, incomplete outcome data was at low risk of bias.
“Fully reported attrition”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn the Basler 1997 trial, blinding of outcome assessment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Keefe 1990, incomplete outcome data was judged at low risk of attrition bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Glombiewski 2010b trial, allocation concealment was at unclear risk of bias.
““coordinated by the first author” before study”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Mishra 2000, selective reporting was judged at high risk of reporting bias.
“Partially reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Leeuw 2008, incomplete outcome data was judged at low risk of attrition bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Greco 2004 trial, incomplete outcome data was at unclear risk of bias.
“Attrition fully reported; no test for differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Kole-Snijders 1999, random sequence generation was judged at unclear risk of selection bias.
“independent researcher blindly drew [numbers assigned randomly to patients] and assigned to one of three conditions”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Keefe 1996, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Kaapa 2006, incomplete outcome data was judged at unclear risk of attrition bias.
“Fully reported; no test for differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Lindell 2008, blinding of outcome assessment was judged at high risk of detection bias.
“Assessors not blind to treatment condition, except for sick listing outcome”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn the Greco 2004 trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Keefe 1996, allocation concealment was judged at high risk of selection bias.
“Not reported (but equal credibility of treatments rated by participants)”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Study design and conductown dataIn the Glombiewski 2010b trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Haldorsen 1998 trial, blinding of outcome assessment was at unclear risk of bias.
“Assessment by physiotherapists who tried to remain blind to treatment”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Lindell 2008, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Keefe 1996, incomplete outcome data was judged at unclear risk of attrition bias.
“Fully reported; no differential attrition but no test for differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Kole-Snijders 1999, allocation concealment was judged at low risk of selection bias.
“independent researcher”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Parker 1988, random sequence generation was judged at high risk of selection bias.
“using a table of random numbers, subjects were assigned”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn McCarberg 1999, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn McCarberg 1999, random sequence generation was judged at unclear risk of selection bias.
“Patients were randomized using a computer-generated random number list”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Litt 2009, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Lindell 2008, incomplete outcome data was judged at unclear risk of attrition bias.
“Fully reported; no test for differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Greco 2004 trial, random sequence generation was at low risk of bias.
““assigned randomly, based on a software-generated randomization plan””
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Litt 2009, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Leeuw 2008, allocation concealment was judged at low risk of selection bias.
“Sealed envelope; research assistant only could access randomization schedule”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Litt 2009, incomplete outcome data was judged at high risk of attrition bias.
“Attrition not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn the Geraets 2005 trial, blinding of outcome assessment was at low risk of bias.
“Researchers not involved in randomisation collect data”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Lindell 2008, allocation concealment was judged at low risk of selection bias.
“Randomisation generated by independent statistician; in opaque envelopes”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn McCarberg 1999, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Nicassio 1997, incomplete outcome data was judged at low risk of attrition bias.
“Attrition fully reported; differential attrition across groups; no differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Mishra 2000, incomplete outcome data was judged at high risk of attrition bias.
“Attrition not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Litt 2009, random sequence generation was judged at low risk of selection bias.
“Computerised urn randomisation”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Kaapa 2006, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Keefe 1996, random sequence generation was judged at high risk of selection bias.
“randomly assigned”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Parker 1988, selective reporting was judged at high risk of reporting bias.
“Partially reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Kole-Snijders 1999, selective reporting was judged at unclear risk of reporting bias.
“Reported as factor scores”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Mishra 2000, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Kraaimaat 1995, allocation concealment was judged at high risk of selection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Haldorsen 1998, incomplete outcome data was judged at high risk of attrition bias.
“Partially reported; differential attrition; no test of differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Nicassio 1997, allocation concealment was judged at high risk of selection bias.
“Not reported, though credibility ratings equal across treatments”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Mishra 2000, allocation concealment was judged at high risk of selection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Falcao 2008 trial, blinding of outcome assessment was at low risk of bias.
“Evaluation by clinician blind to treatment allocation”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Nicassio 1997, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Kole-Snijders 1999, incomplete outcome data was judged at low risk of attrition bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Haldorsen 1998, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Kaapa 2006, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Keefe 1996, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Mishra 2000, random sequence generation was judged at high risk of selection bias.
“patients were assigned to group in a semi-random fashion using the urn method of random assignment”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Parker 1988, incomplete outcome data was judged at high risk of attrition bias.
“Attrition not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Haldorsen 1998, blinding of outcome assessment was judged at unclear risk of detection bias.
“Data gathered by research team”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn McCarberg 1999, incomplete outcome data was judged at unclear risk of attrition bias.
“No attrition during treatment, only at follow-up; no test for differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Leeuw 2008, blinding of outcome assessment was judged at low risk of detection bias.
“Electronic administration of assessments”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Keefe 1990, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Keefe 1990, random sequence generation was judged at unclear risk of selection bias.
“randomly assigned (using a random number table)”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Keefe 1990, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Litt 2009, allocation concealment was judged at high risk of selection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Leeuw 2008, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Kaapa 2006, random sequence generation was judged at low risk of selection bias.
“Random numbers”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Geraets 2005 trial, random sequence generation was at low risk of bias.
“Block randomisation according to random number table”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Kraaimaat 1995, random sequence generation was judged at high risk of selection bias.
“randomly assigned”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Leeuw 2008, random sequence generation was judged at low risk of selection bias.
“predetermined and computer-generated randomization schedule”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Glombiewski 2010b trial, random sequence generation was at low risk of bias.
“Randomisation by random number generation”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Haldorsen 1998, random sequence generation was judged at unclear risk of selection bias.
“Shuffled sealed envelopes”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Lindell 2008, random sequence generation was judged at low risk of selection bias.
“Computerised block randomisation procedure”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Haldorsen 1998, allocation concealment was judged at low risk of selection bias.
“Sealed envelopes; procedure by researchers blind to participant screening”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Parker 1988, allocation concealment was judged at high risk of selection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Haldorsen 1998 trial, random sequence generation was at low risk of bias.
“Allocated at random by cards in sealed envelopes”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Kraaimaat 1995, incomplete outcome data was judged at unclear risk of attrition bias.
“Fully reported; several differences between dropouts and completers”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Kraaimaat 1995, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn the Glombiewski 2010b trial, blinding of outcome assessment was at high risk of bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn the Geraets 2005 trial, selective reporting was at low risk of bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Kole-Snijders 1999, blinding of outcome assessment was judged at low risk of detection bias.
“Assessor unaware of treatment condition”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Kaapa 2006, allocation concealment was judged at low risk of selection bias.
“Opaque sealed envelopes; numbers generated by independent statistician”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Nicassio 1997, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Kraaimaat 1995, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Keefe 1990, allocation concealment was judged at high risk of selection bias.
“Not reported (but equal credibility of treatments rated by participants)”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn McCarberg 1999, allocation concealment was judged at high risk of selection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn the Glombiewski 2010b trial, incomplete outcome data was at unclear risk of bias.
“Attrition fully reported; statement that dropout data will be reported elsewhere”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataNo dichotomous outcomes were reported so no numbers needed to treat (NNTs) were calculated.
“No dichotomous outcomes were reported so no numbers needed to treat (NNTs) were calculated.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Strauss 1986, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenAssessment of risk of bias in included studies has been expanded to include a fuller description, using the Cochrane Handbook recommendations.
“Assessment of risk of bias in included studies: this has been expanded to include a fuller description, using the Cochrane Handbook recommendations.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Strauss 1986, incomplete outcome data was judged at high risk of attrition bias.
“Attrition not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Hammond 2001, allocation concealment was judged to be at low risk of bias because sealed envelopes were prepared in advance.
“Allocation concealment (selection bias) Low risk Sealed envelopes prepared in advance”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Thorsell 2011, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Thieme 2003, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenWe added 'Risk of bias' ratings for all included studies.
“We added 'Risk of bias' ratings for all included studies.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Parker 1988, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Smeets 2006, incomplete outcome data was judged at unclear risk of attrition bias.
“Attrition fully reported; no test for differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Schmidt 2011, random sequence generation was judged at low risk of selection bias.
“randomized in blocks by a computer algorithm”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Smeets 2006, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenIn Schmidt 2011, allocation concealment was judged at low risk of selection bias.
“Patients and personnel blinded to treatment allocation”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn Thorsell 2011, allocation concealment was judged at high risk of selection bias.
“Not reported, but treatment credibility equal”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Thieme 2003, allocation concealment was judged at high risk of selection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Thorsell 2011, random sequence generation was judged at unclear risk of selection bias.
“randomized by drawing pieces of paper with type of intervention”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Thieme 2003, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Strauss 1986, allocation concealment was judged at high risk of selection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Schmidt 2011, selective reporting was judged at low risk of reporting bias.
“Fully reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Thieme 2003, random sequence generation was judged at high risk of selection bias.
“randomly assigned”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataPlanned subgroup analyses on doses and on different conditions were not undertaken due to lack of data.
“Planned subgroup analyses on doses and on different conditions were not undertaken due to lack of data.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Hammond 2001, incomplete outcome data was judged to be at high risk of bias because attrition was only partially reported and no test for differences was performed.
“Incomplete outcome data (attrition bias) All outcomes High risk Attrition partially reported; no test for differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Puder 1988, random sequence generation was judged at high risk of selection bias.
“randomly assigned”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Hammond 2001, blinding of outcome assessment was judged to be at low risk of bias because an independent assessor was used.
“Blinding of outcome assessment (detection bias) All outcomes Low risk Independent assessor”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductown dataIn Thieme 2003, incomplete outcome data was judged at unclear risk of attrition bias.
“Attrition reported; no test for differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Thorsell 2011, incomplete outcome data was judged at unclear risk of attrition bias.
“Attrition fully reported; no test for differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Hammond 2001, random sequence generation was judged to be at high risk of bias because allocation was described only as 'allocated randomly'.
“Random sequence generation (selection bias) High risk”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Puder 1988, allocation concealment was judged at high risk of selection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenNo adjustment for reliability of measures was made.
“No adjustment for reliability of measures was made.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Puder 1988, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Puder 1988, selective reporting was judged at high risk of reporting bias.
“Partially reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Schmidt 2011, incomplete outcome data was judged at unclear risk of attrition bias.
“Attrition fully reported; no test for differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Strauss 1986, random sequence generation was judged at high risk of selection bias.
“randomly assigned”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Strauss 1986, selective reporting was judged at high risk of reporting bias.
“Partially reported”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Smeets 2006, random sequence generation was judged at low risk of selection bias.
“Randomised in blocks by computer-generated algorithm”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Smeets 2006, allocation concealment was judged at low risk of selection bias.
“Generated by independent statistician; sealed envelopes”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Schmidt 2011, blinding of outcome assessment was judged at low risk of detection bias.
“Assessors blinded”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataData extraction for 46 of the 60 trials in our penultimate selection (77%) was done independently by two authors, and the remainder by one.
“Data extraction for 46 of the 60 trials in our penultimate selection (77%) was done independently by two authors, and the remainder by one.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataIn Puder 1988, incomplete outcome data was judged at unclear risk of attrition bias.
“Attrition reported; no test for differences”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).
Study design and conductnone givenIn Thorsell 2011, blinding of outcome assessment was judged at high risk of detection bias.
“Not reported”
Quote in the paperNot a substantial claim
The paper relies on this without support.
Chronic pain is a common problem causing significant distress and disability.
“Chronic pain is a common problem causing significant distress and disability.”
The paper relies on this without support.
The evidence base for psychological therapies is dominated by studies of programmatic and protocolised treatments from a behavioural or cognitive behavioural tradition of clinical psychology.
“The evidence base for psychological therapies is dominated by studies of programmatic and protocolised treatments from a behavioural or cognitive behavioural tradition of clinical psychology.”
The paper relies on this without support.
Patients in waiting list or treatment as usual conditions receive variable and usually unrecorded treatment.
“Thus patients in these conditions receive variable and usually unrecorded treatment.”
The paper relies on this without support.
Catastrophic thinking has emerged as a predictor of behavioural and emotional outcomes in the longer term, and is a widely used target of cognitive treatment.
“This has emerged as a predictor of behavioural and emotional outcomes in the longer term, and is a widely (if not universally) used target of cognitive treatment.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Only the effect size of mood was maintained at follow-up in Williams et al.'s meta-analysis.
“However, only the effect size of mood was maintained at follow-up (Williams et al., 2012).”
From Acceptance- and mindfulness-based interventions for the treatment of chronic pain: a meta-analytic review (2016) · cites this paper as Williams et al., 2012
The Summary of results says that, for CBT versus treatment as usual or waiting list, the mood effect was maintained at follow-up while pain and disability effects were not. But the unqualified claim overlooks a different comparison: the Cognitive behavioural versus active control at follow-up section reports a significant disability effect and no significant mood effect. (LLM, conf=0.87)
Experimental — accuracy not yet measuredCBT and ACT present the strongest evidence for decreasing depression, pain-related anxiety, and catastrophizing and for increasing self-efficacy.
“From a wide range of psychological therapies, Cognitive Behavioral Therapy (CBT) and Acceptance and Commitment Therapy (ACT) present the strongest evidence for decreasing depression, pain-related anxiety, and catastrophizing and for increasing self-efficacy (Williams et al., 2012; Veehof et al., 2016).”
From The Development of Mindful-Based Dance Movement Therapy Intervention for Chronic Pain: A Pilot Study With Chronic Headache Patients (2021) · cites this paper as Williams et al., 2012
The Summary of results and CBT-versus-treatment-as-usual sections report improvements in mood and catastrophising, supporting part of the claim. The included-studies description lists an ACT-versus-CBT trial and its anxiety measure, but the review does not identify ACT alongside CBT as having the strongest evidence for all four outcomes; it also does not report an overall improvement in pain-related anxiety or self-efficacy. (LLM, conf=0.88)
Experimental — accuracy not yet measuredCBT is effective in reducing disability and catastrophic reaction, whereas its effects on pain intensity are negligible.
“CBT, the most common and successful psychological approach in treating pain, is effective in reducing disability and catastrophic reaction, whereas the effects on pain intensity are negligible.30”
From <p>Pain and Evil: From Local Nociception to Misery Following Social Harm</p> (2020) · cites this paper as [30]
The Disability outcomes and Catastrophising outcomes sections report reductions with CBT, although their size and persistence depend on the comparator and follow-up time. The Pain outcomes section reports no benefit over an active control or at follow-up, but does report a small post-treatment benefit over doing nothing; calling its effect on pain intensity negligible without that qualification understates this finding. (LLM, conf=0.84)
Experimental — accuracy not yet measuredThe effect of MBIs in patients with chronic pain is comparable to that of cognitive behavioural therapy programmes with moderate effect sizes for pain intensity, anxiety, depression, and physical health.
“Regarding effect sizes, the effect of MBIs in patients with chronic pain is comparable to that of cognitive behavioural therapy programmes with moderate effect sizes reported in relation to pain intensity, anxiety, depression, and physical health [10-13].”
From A 13-weeks mindfulness based pain management program improves psychological distress in patients with chronic pain compared with waiting list controls (2016) · cites this paper as [13]
The Pain outcomes and Mood outcomes sections report that CBT had a small effect on pain and a moderate immediate effect on mood compared with doing nothing; effects differed against active controls and at follow-up (page numbers unavailable). The review does not establish moderate effects for each listed outcome—anxiety and physical health are not reported as separate summary outcomes—or directly compare CBT with MBIs. (LLM, conf=0.88)
Experimental — accuracy not yet measuredCBT for chronic pain produces only small to medium effect sizes for pain and related disability, although it is superior to no treatment or treatment as usual.
“While superior in comparison to no treatment or treatment as usual, CBT produces only small to medium effect sizes for pain and related disability. 54”
From The Mediating Role of Acceptance in Multidisciplinary Cognitive-Behavioral Therapy for Chronic Pain (2015) · cites this paper as [54]
The Summary of results and the treatment-as-usual post-treatment analysis report small, significant benefits of CBT for pain and disability immediately after treatment. The claim omits the time limit: the treatment-as-usual follow-up analysis found no significant benefit for either outcome. (LLM, conf=0.86)
Experimental — accuracy not yet measured
Controlled effect sizes for CBT for chronic pain patients usually fall in the small (d=0.2) to moderate range (d=0.5).
“Controlled effect sizes for CBT for chronic pain patients usually fall in the small (d=0.2) to moderate range (d=0.5). 54”
From The Mediating Role of Acceptance in Multidisciplinary Cognitive-Behavioral Therapy for Chronic Pain (2015) · cites this paper as [54]
In “Cognitive behavioural versus treatment as usual posttreatment” (page unavailable), pooled CBT effects range from SMD −0.21 for pain to −0.53 for catastrophising, broadly matching small-to-moderate effects. But “Cognitive behavioural versus active control post-treatment” reports smaller effects, including no significant effect on pain or mood. The claim omits this comparator-dependent qualification. (LLM, conf=0.84)
Experimental — accuracy not yet measuredExercise interventions and psychological therapies such as cognitive behavioural therapy are known to be effective for patients with chronic pain.
“Exercise interventions and psychological therapies, such as cognitive behavioural therapy (CBT), are examples of conservative treatments that are known to be effective for patients with chronic pain [5, 6, 9–12].”
From Exercise combined with Acceptance and Commitment Therapy (ExACT) compared to a supervised exercise programme for adults with chronic pain: study protocol for a randomised controlled trial. (2018) · cites this paper as [6]
The Summary of results (page unavailable) reports small benefits of CBT for some chronic-pain outcomes, supporting the psychological-therapy part of the claim. The review does not establish that exercise interventions are effective, and its CBT findings vary by outcome, comparator and follow-up time. (LLM, conf=0.88)
Experimental — accuracy not yet measuredEffect sizes of cognitive behavioral treatments are modest.
“However, as is the case for biomedical treatment solutions, effect sizes of CBTs are modest (Williams, Eccleston, & Morley, 2012).”
From Acceptance- and mindfulness-based interventions for the treatment of chronic pain: a meta-analytic review (2016) · cites this paper as Williams, Eccleston, & Morley, 2012
Overall, the effect sizes found in this study were at least comparable to those found in a recent meta-analysis of CBT for chronic pain patients (Williams et al., 2012).
“Overall, the effect sizes found in this study were at least comparable to those found in a recent meta-analysis of CBT for chronic pain patients (Williams et al., 2012).”
From Acceptance- and mindfulness-based interventions for the treatment of chronic pain: a meta-analytic review (2016) · cites this paper as Williams et al., 2012
Williams and co-workers found small post treatment effect sizes on pain intensity, disability and mood in their meta-analysis of sixteen RCTs, in which CBT was compared to TAU or a waiting list.
“Williams and co-workers found small post treatment effect sizes on pain intensity, disability and mood in their meta-analysis of sixteen RCTs, in which CBT was compared to TAU or a waiting list.”
From Acceptance- and mindfulness-based interventions for the treatment of chronic pain: a meta-analytic review (2016) · cites this paper as Williams et al., 2012
Blinding of participants and personnel was not assessed because therapists and patients cannot be blinded to treatment delivery or receipt.
“We excluded the option of 'blinding participants and personnel' because neither therapists nor patients can be blinded to whether they deliver or receive treatment (Williams et al., 2012).”
From Efficacy, acceptability and safety of cognitive behavioural therapies in fibromyalgia syndrome – A systematic review and meta-analysis of randomized controlled trials (2018) · cites this paper as Williams et al., 2012
The evidence to support psychological therapies has been questioned, with improvements found to be modest compared with other active treatments.
“Similarly, the evidence to support psychological therapies has been questioned, with improvements found to be modest when compared to other active treatments (Williams et al., 2012).”
From Exercise combined with Acceptance and Commitment Therapy for chronic pain: One-year follow-up from a randomized controlled trial (2024) · cites this paper as Williams et al., 2012
The effect sizes observed in this study were in line with existing literature on in-person PMP effectiveness.
“These effect sizes were in line with existing literature on in-person PMP effectiveness. 1,2”
Cognitive behavioural pain management programmes are effective in reducing co-morbid psychological distress.
“Cognitive behavioural pain management programmes (PMPs) are effective in reducing co‐morbid psychological distress (Williams et al., 2012), but are costly and not widely available (Ehde et al., 2014).”
From Five-year observational study of Internet-delivered cognitive behavioural pain management when offered as routine care by an online therapy clinic (2022) · cites this paper as Williams et al., 2012
CBT interventions for chronic pain have demonstrated beneficial effects on pain, disability, HRQoL, and mood in multiple populations.
“In other chronic pain conditions, cognitive-behavioral therapy (CBT) has demonstrated efficacy in improving patient outcomes (e.g., pain-related disability and depression).”
From Internet Cognitive-Behavioral Therapy for Painful Chronic Pancreatitis: A Pilot Feasibility Randomized Controlled Trial (2021) · cites this paper as [9]
Our findings extend the evidence base of CBT, which has been extensively studied in other chronic pain conditions.
“Our findings extend the evidence base of CBT, which has been extensively studied in other chronic pain conditions (9).”
From Internet Cognitive-Behavioral Therapy for Painful Chronic Pancreatitis: A Pilot Feasibility Randomized Controlled Trial (2021) · cites this paper as [9]
Cognitive Behavioral Therapy (on which PMPs are based) is an effective intervention in the management of chronic pain.
“An early systematic review in 1999 [28], which was subsequently updated in 2012 as a Cochrane review [29], concluded that Cognitive Behavioral Therapy (CBT) (on which PMPs are based) is an effective intervention in the armoury of the management of chronic pain.”
Mostly small to moderate effect sizes on disability, mood, catastrophizing, and pain have been reported for CBT; long-term effects are unclear; and the diversity of CBT interventions has made it hard to identify treatment mechanisms.
“Mostly small to moderate effect sizes on disability, mood, catastrophizing and pain have been reported, longterm effects are unclear, and the diversity of CBT interventions has made it hard to identify treatment mechanisms (Eccleston et al., 2009;Morley et al., 2013;Williams et al., 2012).”
From Internet-delivered acceptance and commitment therapy as microlearning for chronic pain: A randomized controlled trial with 1-year follow-up (2021) · cites this paper as Williams et al., 2012
The effect sizes in this study were mostly larger than seen previously, both compared to Internet-ACT studies and benchmark effect sizes from the most recent Cochrane reviews for Internet-CBT and face-to-face CBT compared to WLC.
“The effect sizes in this study were mostly larger than seen previously, both compared to Internet-ACT studies (see below), and benchmark effect sizes from the most recent Cochrane reviews for Internet-CBT (pooled disability/ interference 0.50, pain intensity 0.37) and face-to-face CBT (pooled disability/interference 0.26, pain intensity 0.21) compared to WLC (Eccleston et al., 2014;Williams et al.”
From Internet-delivered acceptance and commitment therapy as microlearning for chronic pain: A randomized controlled trial with 1-year follow-up (2021) · cites this paper as Williams et al., 2012
The long-term effects of cognitive behavioural therapy for chronic pain are quite modest.
“In comparison, the long-term effects of cognitive behavioural therapy for chronic pain are quite modest [13].”
From A 13-weeks mindfulness based pain management program improves psychological distress in patients with chronic pain compared with waiting list controls (2016) · cites this paper as [13]
Cognitive Behavioral Therapy (CBT) is the most widely used psychological treatment for adults with chronic pain and is considered a standard treatment.
“At present Cognitive Behavioral Therapy (CBT) is the most widely used psychological treatment for adults with chronic pain and is considered a standard treatment. 54”
From The Mediating Role of Acceptance in Multidisciplinary Cognitive-Behavioral Therapy for Chronic Pain (2015) · cites this paper as [54]
A recent Cochrane review concludes that CBT is useful for chronic pain and that there is no need for further RCTs focusing on the reporting of group mean values.
“A recent Cochrane review concludes that CBT is useful for chronic pain and that there is no need for further RCTs focusing on the reporting of group mean values [17].”
From Acceptance as a Mediator for Change in Acceptance and Commitment Therapy for Persons with Chronic Pain? (2016) · cites this paper as [17]
Cognitive behavioural therapy has small to moderate effects on pain, disability, mood and catastrophising in chronic pain.
“A Cochrane review concluded that CBT has small to moderate effects on pain, disability, mood and catastrophising [6].”
The effects of available chronic pain interventions on pain and disability are modest and improvements are typically short term.
“There is a plethora of treatment options available but the effects of these interventions on pain and disability are modest and improvements are typically short term [5, 6].”
The authors kept the minimum criterion of 20 participants per arm at the end of treatment assessment, as in the 2012 update.
“We kept the minimum criterion of 20 participants per arm at the end of treatment assessment, as in the 2012 update (Williams 2012).”
From Psychological therapies for the management of chronic pain (excluding headache) in adults (2020) · cites this paper as Williams 2012
The conclusions of this update are broadly in line with the conclusions of the previous version (Williams 2012), although over 50% of the studies in this update are new.
“The conclusions of this update are broadly in line with the conclusions of the previous version (Williams 2012), although over 50% of the studies in this update are new.”
From Psychological therapies for the management of chronic pain (excluding headache) in adults (2020) · cites this paper as Williams 2012
Our results in relation to the active control comparator are in concordance with a previous meta-analysis on traditional psychological therapies for chronic pain, which concluded that there was no evidence of efficacy of CBT and behavioral therapy on pain.
“Our results in relation to the active control comparator are in concordance with a previous meta-analysis on traditional psychological therapies for chronic pain, which concluded that there was no evidence of efficacy of CBT and behavioral therapy on pain [65].”
From Tailored web-based interventions for pain: Systematic review and meta-analysis (2017) · cites this paper as [65]
Other systematic reviews and meta-analyses on Web-based CBT, as well as traditional CBT, also reported small effects in the reduction of pain posttreatment compared with standard care or waiting list.
“Other systematic reviews and meta-analyses on Web-based CBT [15,18,19], as well as traditional CBT [65], also reported small effects in the reduction of pain posttreatment compared with standard care or waiting list.”
From Tailored web-based interventions for pain: Systematic review and meta-analysis (2017) · cites this paper as [65]
Cognitive behavioral therapy is recognized and recommended as an effective treatment for managing chronic pain.
“Cognitive behavioral therapy is known to improve the management of chronic pain.”
A previous review had shown small-to-moderate effect size of catastrophic thinking and mood.
“We expected improvement of cognition-related pain-related catastrophic thoughts, anxiety, and depressive symptoms, because a previous review had shown small-to-moderate effect size of catastrophic thinking and mood [9].”
The latest systematic review of 75 RCTs about the effectiveness of face-to-face CBT showed that CBT versus TAU at the treatment end for pain, disability, and distress showed a small effect size, and versus active treatment showed few effects (n=9401).
“The latest systematic review of 75 RCTs about the effectiveness of face-to-face CBT has shown that CBT versus TAU at the treatment end for pain, disability, and distress showed a small effect size, and versus active treatment showed few effects (n=9401) [9].”
There is a consensus in the literature that future improvements in outcomes from CBT for chronic pain will require research to identify patient and treatment variables that help explain outcomes.
“There is now a consensus in the literature that future improvements in outcomes obtained from cognitive behavioral therapy (CBT) for chronic pain will require research to identify patient and treatment variables that help explain outcomes.”
From Predictors and mediators of outcome in cognitive behavioral therapy for chronic pain: The contributions of psychological flexibility (2021) · cites this paper as Williams et al., 2012
Effect sizes for pain and related disability in CBT for chronic pain tend to fall in the small to moderate range.
“Effect sizes for pain and related disability tend to fall in the small to moderate range, and little is known about who is most likely to benefit from this treatment, the appropriate dose, the format (group versus individual), or the necessary treatment components (Turner, Holtzman, & Mancl, 2007; Williams et al., 2012).”
From Predictors and mediators of outcome in cognitive behavioral therapy for chronic pain: The contributions of psychological flexibility (2021) · cites this paper as Williams et al., 2012
Little is known about who is most likely to benefit from CBT for chronic pain, the appropriate dose, the format (group versus individual), or the necessary treatment components.
“Effect sizes for pain and related disability tend to fall in the small to moderate range, and little is known about who is most likely to benefit from this treatment, the appropriate dose, the format (group versus individual), or the necessary treatment components (Turner, Holtzman, & Mancl, 2007; Williams et al., 2012).”
From Predictors and mediators of outcome in cognitive behavioral therapy for chronic pain: The contributions of psychological flexibility (2021) · cites this paper as Williams et al., 2012
The sample size of 232 was sufficient to detect a pre-treatment to 12-month follow-up effect size of d = .2, with 80% power, and p = .05.
“Using a conservative approach our power analysis indicated that the sample size of 232 was sufficient to detect a pre-treatment to 12-month follow-up effect size of d = .2, with 80% power, and p = .05 (Williams et al., 2012).”
From Predictors and mediators of outcome in cognitive behavioral therapy for chronic pain: The contributions of psychological flexibility (2021) · cites this paper as Williams et al., 2012
Multicomponent cognitive behavioral therapy (CBT) is superior to treatment as usual and no treatment (but not other active treatments) for adults with chronic pain arising from various conditions (excluding headaches).
“Systematic and meta-analytic reviews find that multicomponent cognitive behavioral therapy (CBT) is superior to treatment as usual and no treatment (but not other active treatments) for adults with chronic pain arising from various conditions (excluding headaches) (Ehde, Dillworth, & Turner, 2014; Williams, Eccleston, & Morley, 2012).”
From Predictors and mediators of outcome in cognitive behavioral therapy for chronic pain: The contributions of psychological flexibility (2021) · cites this paper as Williams, Eccleston, & Morley, 2012
Studies of multicomponent CBT programs for chronic pain have not yet revealed which individual treatment components are necessary, and for whom, to achieve improved outcomes.
“Studies of multicomponent CBT programs for chronic pain have not yet revealed which individual treatment components are necessary, and for whom, to achieve improved outcomes (Vowles et al., 2009; Williams et al., 2012).”
From Predictors and mediators of outcome in cognitive behavioral therapy for chronic pain: The contributions of psychological flexibility (2021) · cites this paper as Williams et al., 2012
The findings correspond with earlier studies from this clinic and with the treatment outcome literature more broadly, which finds that such programs are empirically-supported and moderately effective forms of psychosocial treatment for chronic pain.
“These findings correspond with earlier studies from this clinic (Åkerblom et al., 2015) and with the treatment outcome literature more broadly, finding that such programs are empirically-supported and moderately effective forms of psychosocial treatment for chronic pain (Williams et al., 2012).”
From Predictors and mediators of outcome in cognitive behavioral therapy for chronic pain: The contributions of psychological flexibility (2021) · cites this paper as Williams et al., 2012
The results of the current study are in line with the general finding that it is difficult to demonstrate reduction in pain levels in well-controlled studies.
“The results of the current study are in line with the general finding that it is difficult to demonstrate reduction in pain levels in well-controlled studies [22, 23].”
From Psychological interventions improve quality of life despite persistent pain in endometriosis: results of a 3-armed randomized controlled trial (2023) · cites this paper as [22]
A carefully matched non-specific control condition has not been used in previous studies.
“Importantly, it appears that a carefully matched non-specific control condition has not been used in previous studies [22, 23, 28, 51, 55]”
From Psychological interventions improve quality of life despite persistent pain in endometriosis: results of a 3-armed randomized controlled trial (2023) · cites this paper as [22]
Statistics recomputed
Every reported test result, recomputed from its test statistic and degrees of freedom. A result shows as not adding up only once an independent check has confirmed it.
- Consistentz = 1.43reported p > .05 · recomputed p = .153
“(Z = 1.43,p > .05”
- Consistentz = 2.66reported p < .01 · recomputed p = .008
“(Z = 2.66, p < .01”
- Consistentz = 0.72reported p > .05 · recomputed p = .472
“(Z = 0.72, p > .05”
- Consistentz = 1.92reported p = .05 · recomputed p = .055
“Z = 1.92,p = .05”
- Consistentz = 1.12reported p > .05 · recomputed p = .263
“(Z = 1.12,p > .05”
- Consistentz = 2.28reported p < .05 · recomputed p = .023
“(Z = 2.28, p < .05”
- Consistentz = 1.15reported p > .05 · recomputed p = .250
“(Z = 1.15,p > .05”
- Consistentz = 0.49reported p > .05 · recomputed p = .624
“Z = 0.49, p > .05”
- Consistentz = 2.59reported p < .05 · recomputed p = .010
“(Z = 2.59, p < .05”
- Consistentz = 2.35reported p < .05 · recomputed p = .019
“(Z = 2.35, p < .05”
- Consistentz = 3.84reported p < .01 · recomputed p < .001
“(Z = 3.84, p < .01”
- Consistentz = 4.58reported p < .01 · recomputed p < .001
“Z = 4.58, p < .01”
- Consistentz = 0.99reported p > .05 · recomputed p = .322
“(Z = 0.99, p > .05”
- Consistentz = 0.66reported p > .05 · recomputed p = .509
“(Z = 0.66, p > .05”
- Consistentz = 1.99reported p = .05 · recomputed p = .047
“(Z = 1.99,p = .05”
- Consistentz = 0.84reported p > .05 · recomputed p = .401
“Z = 0.84, p > .05”
- Consistentz = 0.77reported p > .05 · recomputed p = .441
“(Z = 0.77, p > .05”
- Consistentz = 1.46reported p > .05 · recomputed p = .144
“(Z = 1.46,p > .05”
- Consistentz = 1.94reported p = .05 · recomputed p = .052
“(Z = 1.94,p = .05”
- Consistentz = 1.67reported p > .05 · recomputed p = .095
“Z = 1.67,p > .05”
- Consistentz = 0.13reported p > .05 · recomputed p = .897
“(Z = 0.13, p > .05”
- Consistentz = 1.01reported p > .05 · recomputed p = .312
“(Z = 1.01,p > .05”
- Consistentz = 1.55reported p > .05 · recomputed p = .121
“(Z = 1.55,p > .05”
- Consistentz = 0.25reported p > .05 · recomputed p = .803
“Z = 0.25, p > .05”
- Consistentz = 1.05reported p > .05 · recomputed p = .294
“(Z = 1.05,p > .05”
- Consistentz = 1.4reported p > .05 · recomputed p = .162
“(Z = 1.40,p > .05”
- Consistentz = 1.18reported p > .05 · recomputed p = .238
“(Z = 1.18,p > .05”
- Consistentz = 1.99reported p = .05 · recomputed p = .047
“Z = 1.99,p = .05”
- Consistentz = 0.21reported p > .05 · recomputed p = .834
“(Z = 0.21, p > .05”
- Consistentz = 1.08reported p > .05 · recomputed p = .280
“(Z = 1.08,p > .05”
- Consistentz = 0.9reported p > .05 · recomputed p = .368
“(Z = 0.90, p > .05”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Catastrophising benefit at follow-up is claimed despite a nonsignificant result
MajorThe summary says CBT's benefit for catastrophising versus doing nothing was sustained at follow-up. The follow-up analysis reports only one study and a nonsignificant effect.
“in comparison with doing nothing it had a moderate effect post-treatment which was sustained at follow-up.”
“There was only one study of 59 participants in the analysis of the effects of CBT on catastrophising.The overall effect of CBT was not significant: Z = 0.84, P > 0.05 (Analysis 4.4).”
Nonsignificant Analysis 4.2 is described as showing an effect
MinorThe heterogeneity discussion groups Analysis 4.2 among four analyses showing an intervention effect, but the results section explicitly calls its overall effect nonsignificant.
“In the four analyses showing an effect of intervention over control but with high heterogeneity (I > 50%), we undertook further exploratory analyses.”
“The overall effect of CBT was not significant (Z = 0.66, P > 0.05) (Analysis 4.2).”
Sex counts exceed the stated starting sample in Geraets 2005
MinorThe stated numbers of women and men at the start of treatment total 192, exceeding the stated starting sample of 176.
Reported 176 · recomputed 192
“Participants End of treatment n = 158 Start of treatment n = 176 Sex: 109 F, 83 M (at start of treatment)”
Disability analysis has two different Z statistics
MinorThe narrative reports Z = 1.46 for behavioural therapy versus active control post-treatment, while the corresponding Analysis 5.2 reports Z = 1.56.
“The overall effect was not significant (Z = 1.46,P > 0.05) (Analysis 5.2).”
“Test for overall effect: Z=1.56(P=0.12)”
Treatment-quality scale has inconsistent denominators
MinorThe methods define the Yates treatment-quality subscale as ranging from 0 to 9, but the Lindell 2008 entry reports its treatment-quality score out of 6.
“Yates quality scale: total quality = 18/35, design quality = 16/26, treatment quality = 2/6”
“a treatment quality scale (0 to 9) covering stated rationale for treatment, manualisation, therapist training and patient engagement”
The post-treatment arm-size threshold is stated two ways
MinorThe inclusion criteria allow 20 participants in each arm, whereas the subsequent description requires more than 20. A study with exactly 20 in an arm would be treated differently under the two rules.
“had 20 or more participants in each treatment arm at the end of the treatment assessment.”
“This last criterion of N > 20 at post-treatment assessment is an improvement from the Eccleston 2009a review”
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- Authors
- Williams, A. C. D. C., Eccleston, C., & Morley, S.
- Affiliations
- University College London (GB)
- University of Bath (GB)
- University of Leeds (GB)
- Venue
- Cochrane Database of Systematic Reviews
- Publisher
- Wiley
- Published
- 2012-11-14
- Volume
- 11
- Pages
- CD007407-CD007407
- ISSN
- 1361-6137 (ISSN-L)
- 1465-1858
- PMC
- PMC6483325
- OpenAlex
- W1955446149
- Semantic Scholar
- 8018a1d7b6374a784decc549b0fb6bb0de863f57
- Cited by
- 1,634
- References
- 293
- Citations by year
- 2026: 12 · 2025: 94 · 2024: 126 · 2023: 114 · 2022: 144 · 2021: 160 · 2020: 106 · 2019: 133 · 2018: 111 · 2017: 115 · 2016: 117 · 2015: 104 · 2014: 102 · 2013: 82 · 2012: 40
- FWCI
- 11.78
- Type
- journal article
- Language
- en
- Update notices
- new_version (2020-08-14)
- Open access
- bronze
- doi.org
- Locations
- Cochrane Database of Systematic Reviews (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- American Heart Association
- Pfizer
- Deutsches Krebsforschungszentrum
- National Institute for Health and Care Research
- ZonMw
- National Institutes of Health (5-R01-)
- National Center for Research Resources (-00056)
- Topics
- Health Sciences › Medicine › Pharmacology › Musculoskeletal pain and rehabilitation
- Health Sciences › Medicine › Anesthesiology and Pain Medicine › Pain Management and Treatment
- Social Sciences › Psychology › Clinical Psychology › Mindfulness and Compassion Interventions
- Keywords
- chronic non-cancer pain, psychotherapy, cognitive behavioral therapy, behavior therapy, acceptance and commitment therapy, fibromyalgia, chronic low back pain, rheumatoid arthritis, pain intensity, disability, psychological distress, adverse events, treatment safety, treatment efficacy, adults, risk of bias, quality of evidence, economic burden, health care costs, treatment expectations, selective reporting
- MeSH terms
- Adult, Affect, Behavior Therapy, Humans, Cognitive Behavioral Therapy, Randomized Controlled Trials as Topic, Chronic Pain
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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