Cited by 1,634Musculoskeletal pain and rehabilitationPain Management and TreatmentMindfulness and Compassion Interventions

Psychological therapies for the management of chronic pain (excluding headache) in adults

Open access
Williams, Amanda C de C, Eccleston, Christopher, Morley, Stephen·2012·Cochrane Database of Systematic Reviews

Abstract

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

AI snapshot

Written from the paper’s full text.

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.

Model-written summary. Check it against the paper before relying on it.

Integrity signals

Registry

Crossref · 10.1002/14651858.cd007407.pub3

Cites

300 of 300 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

0 of 38 cited sources checked · 0 supported · 0 flagged

  • 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
  • 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 data

    The 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 claim
  • May combine two claims.

    Findingown data

    Of 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 claim
  • May combine two claims.

    Findingown data

    The 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 claim
  • May combine two claims.

    Findingown data

    N 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingnone given

    Treatment 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 claim
  • May combine two claims.

    Findingown data

    This 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 claim
  • May combine two claims.

    Findingown data

    Of 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 claim
  • The quote only partly states this claim.

    Findingown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingown data

    Before 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 claim
  • May combine two claims.

    Findingown data

    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.

    “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 claim
  • The quote only partly states this claim.

    Findingown data

    In 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 claim
  • May combine two claims.

    Findingown data

    In 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 given

    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).

    “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 claim
  • May combine two claims.

    Findingreasoning

    For 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Findingnone given

    The 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 claim
  • May combine two claims.

    Findingown data

    In 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 data

    The 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 claim
  • The quote only partly states this claim.

    Findingown data

    CBT has a moderate effect on catastrophising at follow-up compared with doing nothing (sustained).

    “which was sustained at follow-up.”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Findingown data

    In 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

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  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Findingcitation

    The 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 data

    Excluding 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 claim
  • The quote only partly states this claim.

    Findingown data

    In 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 claim
  • May combine two claims.

    Findingown data

    In 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 data

    Of 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 claim
  • May combine two claims.

    Findingnone given

    Compared 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 given

    Numbers 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 claim
  • May combine two claims.

    Findingcitation

    The 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

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    • cites Butler 2006 source

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  • May combine two claims.

    Findingcitation

    Treatment 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 checked
    • cites Glombiewski 2010

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    • cites Fairbank 2005 source

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    • cites Hellum 2011 source

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  • May combine two claims.

    Findingcitation

    The 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

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  • May combine two claims.

    Findingnone given

    No 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 claim
  • May combine two claims.

    Findingnone given

    The 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 claim
  • Probably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing). May combine two claims.

    Premisecitation

    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.

    “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

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  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductcitation

    We 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

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  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Premisecitation

    Behavioural 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

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    • cites Keefe Rumble 2004

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  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Study design and conductown data

    Two 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 claim
  • May combine two claims.

    Study design and conductown data

    14 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Premisecitation

    The 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

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  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Study design and conductreasoning

    We 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 claim
  • May combine two claims.

    Study design and conductown data

    Fifteen 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 claim
  • Probably not a substantial claim: may not pass S2 (checkable). May combine two claims.

    Premisecitation

    This 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

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  • May combine two claims.

    Study design and conductown data

    13 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 claim
  • Classified as probably not a substantial claim.

    Study design and conductcitation

    We 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 checked
    • cites Ioannidis 2005 source

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    • cites Nuesch 2009 source

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    Study design and conductown data

    34 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 claim
  • May combine two claims.

    Premisecitation

    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.

    “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

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  • May combine two claims.

    Premisecitation

    Against 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

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  • May combine two claims.

    Study design and conductown data

    16 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 claim
  • May combine two claims.

    Premisecitation

    Against 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 data

    Mean 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 claim
  • Classified as probably not a substantial claim.

    Study design and conductcitation

    We 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.

    Interpretationreasoning

    Trials 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Premisecitation

    Behaviour 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 data

    In the Evers 2002 trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductreasoning

    In 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 claim
  • May combine two claims.

    Interpretationown data

    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.

    “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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In the Evers 2002 trial, blinding of outcome assessment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S2 (checkable).

    Interpretationnone given

    It 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductreasoning

    In the Evers 2002 trial, allocation concealment was at low risk of bias.

    ““previously determined””
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In the Bliokas 2007 trial, allocation concealment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In the Altmaier 1992 trial, blinding of outcome assessment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductreasoning

    In the De Souza 2008 trial, allocation concealment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductown data

    In the Evers 2002 trial, incomplete outcome data was at low risk of bias.

    “Attrition fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In the Ersek 2008 trial, allocation concealment was at low risk of bias.

    “By independent statistician”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductreasoning

    In the Altmaier 1992 trial, allocation concealment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Interpretationcitation

    Although 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 checked
    • cites Fairbank 2005 source

      Not checked in the free run.

    • cites Hellum 2011 source

      Not checked in the free run.

    • cites Morley 2008 source

      Not checked in the free run.

  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In the Evers 2002 trial, random sequence generation was at unclear risk of bias.

    “Random numbers”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Interpretationnone given

    Psychological 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In the Ersek 2008 trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductown data

    In the Falcao 2008 trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In the Altmaier 1992 trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In the Buckelew 1998 trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In the Bliokas 2007 trial, incomplete outcome data was at low risk of bias.

    “Attrition fully reported; no differences”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductreasoning

    In the Buckelew 1998 trial, allocation concealment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductreasoning

    In the Falcao 2008 trial, allocation concealment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In the Ersek 2008 trial, blinding of outcome assessment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In the Ehrenborg 2010 trial, incomplete outcome data was at low risk of bias.

    “Attrition fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductreasoning

    In the Ehrenborg 2010 trial, allocation concealment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Interpretationreasoning

    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.

    “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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In the Bliokas 2007 trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductown data

    In the Basler 1997 trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In the De Souza 2008 trial, blinding of outcome assessment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductreasoning

    In the De Souza 2008 trial, random sequence generation was at high risk of bias.

    ““randomly assigned””
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductreasoning

    In the Basler 1997 trial, allocation concealment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In the Ehrenborg 2010 trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In the Bliokas 2007 trial, random sequence generation was at low risk of bias.

    “Random numbers generation”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In the De Souza 2008 trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In the Ersek 2008 trial, incomplete outcome data was at low risk of bias.

    “Fully reported attrition”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In the Basler 1997 trial, blinding of outcome assessment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Keefe 1990, incomplete outcome data was judged at low risk of attrition bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Mishra 2000, selective reporting was judged at high risk of reporting bias.

    “Partially reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Leeuw 2008, incomplete outcome data was judged at low risk of attrition bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Keefe 1996, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductown data

    In the Greco 2004 trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).

    Study design and conductown data

    In the Glombiewski 2010b trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Lindell 2008, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductreasoning

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Kole-Snijders 1999, allocation concealment was judged at low risk of selection bias.

    “independent researcher”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In McCarberg 1999, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Litt 2009, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In Litt 2009, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Litt 2009, incomplete outcome data was judged at high risk of attrition bias.

    “Attrition not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductreasoning

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In McCarberg 1999, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Mishra 2000, incomplete outcome data was judged at high risk of attrition bias.

    “Attrition not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Litt 2009, random sequence generation was judged at low risk of selection bias.

    “Computerised urn randomisation”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Kaapa 2006, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Keefe 1996, random sequence generation was judged at high risk of selection bias.

    “randomly assigned”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Parker 1988, selective reporting was judged at high risk of reporting bias.

    “Partially reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Kole-Snijders 1999, selective reporting was judged at unclear risk of reporting bias.

    “Reported as factor scores”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Mishra 2000, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Kraaimaat 1995, allocation concealment was judged at high risk of selection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Mishra 2000, allocation concealment was judged at high risk of selection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Nicassio 1997, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Kole-Snijders 1999, incomplete outcome data was judged at low risk of attrition bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Haldorsen 1998, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In Kaapa 2006, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In Keefe 1996, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In Parker 1988, incomplete outcome data was judged at high risk of attrition bias.

    “Attrition not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductreasoning

    In Leeuw 2008, blinding of outcome assessment was judged at low risk of detection bias.

    “Electronic administration of assessments”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Keefe 1990, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In Keefe 1990, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Litt 2009, allocation concealment was judged at high risk of selection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Leeuw 2008, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Kaapa 2006, random sequence generation was judged at low risk of selection bias.

    “Random numbers”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Kraaimaat 1995, random sequence generation was judged at high risk of selection bias.

    “randomly assigned”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In the Glombiewski 2010b trial, random sequence generation was at low risk of bias.

    “Randomisation by random number generation”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Haldorsen 1998, random sequence generation was judged at unclear risk of selection bias.

    “Shuffled sealed envelopes”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Lindell 2008, random sequence generation was judged at low risk of selection bias.

    “Computerised block randomisation procedure”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Parker 1988, allocation concealment was judged at high risk of selection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Kraaimaat 1995, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In the Glombiewski 2010b trial, blinding of outcome assessment was at high risk of bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In the Geraets 2005 trial, selective reporting was at low risk of bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In Nicassio 1997, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In Kraaimaat 1995, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductreasoning

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In McCarberg 1999, allocation concealment was judged at high risk of selection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Study design and conductown data

    No 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Strauss 1986, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    Assessment 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In Strauss 1986, incomplete outcome data was judged at high risk of attrition bias.

    “Attrition not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In Thorsell 2011, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In Thieme 2003, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    We 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Parker 1988, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Smeets 2006, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductreasoning

    In Thorsell 2011, allocation concealment was judged at high risk of selection bias.

    “Not reported, but treatment credibility equal”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Thieme 2003, allocation concealment was judged at high risk of selection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Thieme 2003, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Strauss 1986, allocation concealment was judged at high risk of selection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In Schmidt 2011, selective reporting was judged at low risk of reporting bias.

    “Fully reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Thieme 2003, random sequence generation was judged at high risk of selection bias.

    “randomly assigned”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Study design and conductown data

    Planned 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Puder 1988, random sequence generation was judged at high risk of selection bias.

    “randomly assigned”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Puder 1988, allocation concealment was judged at high risk of selection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    No adjustment for reliability of measures was made.

    “No adjustment for reliability of measures was made.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Puder 1988, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Puder 1988, selective reporting was judged at high risk of reporting bias.

    “Partially reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Strauss 1986, random sequence generation was judged at high risk of selection bias.

    “randomly assigned”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Strauss 1986, selective reporting was judged at high risk of reporting bias.

    “Partially reported”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Smeets 2006, allocation concealment was judged at low risk of selection bias.

    “Generated by independent statistician; sealed envelopes”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Schmidt 2011, blinding of outcome assessment was judged at low risk of detection bias.

    “Assessors blinded”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    Data 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 claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In 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 claim
  • Probably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing), S4 (based).

    Study design and conductnone given

    In Thorsell 2011, blinding of outcome assessment was judged at high risk of detection bias.

    “Not reported”
    Quote in the paperNot a substantial claim
208 of 208
  • 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.”
4 of 4

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 measured
  • CBT 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 measured
  • CBT 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 &lt;p&gt;Pain and Evil: From Local Nociception to Misery Following Social Harm&lt;/p&gt; (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 measured
  • The 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 measured
  • CBT 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

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”

31 of 31

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

    Major

    The 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.

  • Nonsignificant Analysis 4.2 is described as showing an effect

    Minor

    The heterogeneity discussion groups Analysis 4.2 among four analyses showing an intervention effect, but the results section explicitly calls its overall effect nonsignificant.

  • Sex counts exceed the stated starting sample in Geraets 2005

    Minor

    The stated numbers of women and men at the start of treatment total 192, exceeding the stated starting sample of 176.

    Reported 176 · recomputed 192

  • Disability analysis has two different Z statistics

    Minor

    The narrative reports Z = 1.46 for behavioural therapy versus active control post-treatment, while the corresponding Analysis 5.2 reports Z = 1.56.

  • Treatment-quality scale has inconsistent denominators

    Minor

    The 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.

  • The post-treatment arm-size threshold is stated two ways

    Minor

    The 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.

6 of 6

Cites

2 retracted

Flagged first, then by citations

Research works printed but not linked: 6

  1. Jensen, 2005, A 3-year follow-up of a multidisciplinary rehabilitation programme for back and neck pain, Pain, 115, 273, 10.1016/j.pain.2005.03.005 · DOI · Paper page
  2. Corrado, 2003, The effect of biofeedback and relaxation training on anxiety and somatic complaints in chronic pain patients, American Journal of Pain Management, 13, 133
  3. Ferrari, 2006, Individual characteristics and results of biofeedback training and operant treatment in patients with chronic pain, Psicoterapia Cognitiva e Comportmentale, 12, 161
  4. Schulze, 2008, Conception and evaluation of a group therapy intervention for patients with chronic pain disorders and applications for early retirement pensions, Rehabilitation, 47, 211
  5. Bowling, 1997, Measuring Health
  6. Garratt, 2008, Patient reported outcomes in trial, BMJ, 337, a1190

Cited by

Sorted by citations

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
OpenAlex
W1955446149
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
Open access
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

About these checks

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.

Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-09.

Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-09.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

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