Cited by 72Chronic Obstructive Pulmonary Disease (COPD) ResearchAnxiety, Depression, Psychometrics, Treatment, Cognitive ProcessesCardiac Health and Mental Health

Psychological therapies for the treatment of anxiety disorders in chronic obstructive pulmonary disease

Open access
Usmani, Zafar A, Carson, Kristin V, Heslop, Karen, Esterman, Adrian J, De Soyza, Anthony, Smith, Brian J·2017·Cochrane Database of Systematic Reviews

Abstract

Background: Chronic obstructive pulmonary disease (COPD) (commonly referred to as chronic bronchitis and emphysema) is a chronic lung condition characterised by the inflammation of airways and irreversible destruction of pulmonary tissue leading to progressively worsening dyspnoea. It is a leading international cause of disability and death in adults. Evidence suggests that there is an increased prevalence of anxiety disorders in people with COPD. The severity of anxiety has been shown to correlate with the severity of COPD, however anxiety can occur with all stages of COPD severity. Coexisting anxiety and COPD contribute to poor health outcomes in terms of exercise tolerance, quality of life and COPD exacerbations. The evidence for treatment of anxiety disorders in this population is limited, with a paucity of evidence to support the efficacy of medication-only treatments. It is therefore important to evaluate psychological therapies for the alleviation of these symptoms in people with COPD. Objectives: To assess the effects of psychological therapies for the treatment of anxiety disorders in people with chronic obstructive pulmonary disease. Search methods: We searched the specialised registers of two Cochrane Review Groups: Cochrane Common Mental Disorders (CCMD) and Cochrane Airways (CAG) (to 14 August 2015). The specialised registers include reports of relevant randomised controlled trials from The Cochrane Library, MEDLINE, Embase, and PsycINFO. We carried out complementary searches on PsycINFO and CENTRAL to ensure no studies had been missed. We applied no date or language restrictions. Selection criteria: We considered all randomised controlled trials (RCTs), cluster-randomised trials and cross-over trials of psychological therapies for people (aged over 40 years) with COPD and coexisting anxiety disorders (as confirmed by recognised diagnostic criteria or a validated measurement scale), where this was compared with either no intervention or education only. We included studies in which the psychological therapy was delivered in combination with another intervention (co-intervention) only if there was a comparison group that received the co-intervention alone. Data collection and analysis: Two review authors independently screened citations to identify studies for inclusion and extracted data into a pilot-tested standardised template. We resolved any conflicts that arose through discussion. We contacted authors of included studies to obtain missing or raw data. We performed meta-analyses using the fixed-effect model and, if we found substantial heterogeneity, we reanalysed the data using the random-effects model. Main results: We identified three prospective RCTs for inclusion in this review (319 participants available to assess the primary outcome of anxiety). The studies included people from the outpatient setting, with the majority of participants being male. All three studies assessed psychological therapy (cognitive behavioural therapy) plus co-intervention versus co-intervention alone. We assessed the quality of evidence contributing to all outcomes as low due to small sample sizes and substantial heterogeneity in the analyses. Two of the three studies had prespecified protocols available for comparison between prespecified methodology and outcomes reported within the final publications. We observed some evidence of improvement in anxiety over 3 to 12 months, as measured by the Beck Anxiety Inventory (range from 0 to 63 points), with psychological therapies performing better than the co-intervention comparator arm (mean difference (MD) -4.41 points, 95% confidence interval (CI) -8.28 to -0.53; P = 0.03). There was however, substantial heterogeneity between the studies (I2 = 62%), which limited the ability to draw reliable conclusions. No adverse events were reported. Authors' conclusions: We found only low-quality evidence for the efficacy of psychological therapies among people with COPD with anxiety. Based on the small number of included studies identified and the low quality of the evidence, it is difficult to draw any meaningful and reliable conclusions. No adverse events or harms of psychotherapy intervention were reported. A limitation of this review is that all three included studies recruited participants with both anxiety and depression, not just anxiety, which may confound the results. We downgraded the quality of evidence in the 'Summary of findings' table primarily due to the small sample size of included trials. Larger RCTs evaluating psychological interventions with a minimum 12-month follow-up period are needed to assess long-term efficacy. © 2017 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

Integrity signals

Registry

Crossref · 10.1002/14651858.cd010673.pub2

Cites

91 of 91 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Claims the paper makes

11 of 82 cited sources checked · 7 supported · 1 flagged · accuracy not yet measured

  • Premisecitation

    There is an increased prevalence of anxiety disorders in people with COPD.

    “Evidence suggests that there is an increased prevalence of anxiety disorders in people with COPD (Maurer 2008).”
    Quote in the paperSubstantial claim1 of 1 sources checked
    • cites Maurer 2008 source
  • Findingown data

    The mean quality of life - emotional composite in the intervention groups was 0.30 standard deviations lower (1.03 lower to 0.44 higher).

    “The mean quality of life -emotional composite in the intervention groups was 0.30 standard deviations lower (1.03 lower to 0.44 higher)”
    Quote in the paperNot a substantial claim
  • Findingown data

    The mean exercise capacity in the intervention groups was 2.78 lower (58.49 lower to 52.94 higher).

    “The mean exercise capacity in the intervention groups was 2.78 lower (58.49lower to 52.94 higher)”
    Quote in the paperNot a substantial claim
  • Findingown data

    For quality of life - physical composite, the short-term follow-up SMD was -0.22 (95% CI -0.45 to 0.01; P = 0.06).

    “short-term (0 to 3 months; SMD -0.22, 95% CI -0.45 to 0.01; P = 0.06)”
    Quote in the paperNot a substantial claim
  • Findingown data

    Beneficial findings were observed in favour of the psychological therapy group for anxiety (p = 0.03).

    “Beneficial findings were observed in favour of the psychological therapy group (p= 0.03)”
    Quote in the paperSubstantial claim
  • Classified as probably not a substantial claim. 57
  • May combine two claims. 45
  • The quote only partly states this claim. 3
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    Another systematic review and meta-analysis of complex interventions for depression and anxiety in COPD identified 28 studies for inclusion.

    “Another systematic review and metaanalysis of complex interventions for depression and anxiety in COPD identified 28 studies for inclusion (Coventry 2013).”
    Quote in the paperNot a substantial claim1 of 1 sources checked
    • cites Coventry 2013 source

      The paper is a systematic review and meta-analysis of complex interventions for depression and anxiety in COPD, but its Characteristics of Populations section says 32 studies met the inclusion criteria, not 28. The Abstract reports that 29 trials were included in the meta-analysis. (LLM, conf=0.91)

      Checked by a reasoning model — may be wrong.

      Experimental — accuracy not yet measured
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    Prevalence rates for anxiety disorders in people with COPD are 28%-36%.

    “Studies have suggested prevalence rates for anxiety disorders of 28%-36% in people with COPD (Di Marco 2006;Yohannnes 2006).”
    Quote in the paperNot a substantial claim1 of 2 sources checked
    • cites Di Marco 2006 source
    • cites Yohannnes 2006

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

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

    Premisecitation

    The severity of anxiety correlates with the severity of COPD and the presence of lower PaO.

    “Moreover, the severity of anxiety has been shown to correlate with the severity of COPD and the presence of lower PaO (partial pressure of oxygen in the blood, an indicator of severity of COPD) (Elassal 2014).”
    Quote in the paperNot a substantial claim1 of 1 sources checked
    • cites Elassal 2014 source
  • May combine two claims.

    Premisecitation

    COPD is associated with a higher risk of anxiety, and co-morbid COPD and anxiety is related to poor health outcomes in terms of exercise tolerance, quality of life, COPD exacerbations, inappropriate use of medications and persistence of smoking as a coping strategy for anxiety management.

    “COPD is associated with a higher risk of anxiety, and co morbid COPD and anxiety is related to poor health outcomes in terms of exercise tolerance, quality of life, COPD exacerbations (Eisner 2010), inappropriate use of medications and persistence of smoking as a coping strategy for anxiety management (Royal College of Physcians).”
    Quote in the paperSubstantial claim1 of 2 sources checked
    • cites Eisner 2010 source
    • cites Royal College of Physcians

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

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

    Premisecitation

    By compromising health status, mood disorders lead to increased risk of hospitalisation and re-hospitalisation and hence also increase direct and indirect costs to the health system.

    “By compromising health status, mood disorders lead to increased risk of hospitalisation and re-hospitalisation (Gudmundsson 2005) and hence also increase direct and indirect costs to the health system.”
    Quote in the paperNot a substantial claim1 of 1 sources checked
    • cites Gudmundsson 2005 source

      The Abstract and Discussion report an increased risk of rehospitalisation among COPD patients with anxiety and low health status. They do not establish that mood disorders cause poor health status or increased hospitalisation generally; the Discussion explicitly reports no association between depression and readmission. The cost statement follows the citation as the citing authors’ inference, rather than a finding attributed to this source. (LLM, conf=0.89)

      Experimental — accuracy not yet measured
  • May combine two claims.

    Premisecitation

    Co-morbid depression is a strong predictor of anxiety, which confounds anxiety symptoms making treatment more difficult.

    “Indeed, co-morbid depression is known to be a strong predictor of anxiety (DiNicola 2013), which confounds anxiety symptoms making treatment more difficult (Atlantis 2013).”
    Quote in the paperNot a substantial claim1 of 2 sources checked
    • cites DiNicola 2013 source
    • cites Atlantis 2013 source
  • May combine two claims.

    Premisecitation

    Among people with COPD, anxiety is related to poorer health outcomes including worse submaximal exercise performance, greater risk of self-reported functional limitations and a higher longitudinal risk of COPD exacerbations.

    “A recent study has shown that among people with COPD, anxiety is related to poorer health outcomes including worse submaximal exercise performance, greater risk of self-reported functional limitations and a higher longitudinal risk of COPD exacerbations (Eisner 2010).”
    Quote in the paperSubstantial claim1 of 1 sources checked
    • cites Eisner 2010 source
  • Classified as probably not a substantial claim.

    Study design and conductcitation

    We used the Chi2 and I2 statistics to quantify inconsistency across studies in combination with visual inspection of the data.

    “We used the Chi 2 (Deeks 2011) and I 2 statistics (Higgins 2003) to quantify inconsistency across studies in combination with visual inspection of the data for differences between studies (e.g.types of interventions, participants etc.).”
    Quote in the paperSubstantial claim1 of 2 sources checked
    • cites Deeks 2011

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

    • cites Higgins 2003 source
  • May combine two claims.

    Premisecitation

    In Coventry 2013, subgroup analyses identified small but non-significant effects on self-reported anxiety symptoms post-treatment for cognitive and behavioural interventions (SMD -0.17; 95% CI -0.35 to 0.01; 7 studies) and relaxation (SMD -0.18; 95% CI -0.67 to 0.30; 3 studies), but no evidence of any effect for self-management education (SMD -0.00; 95% CI -0.17 to 0.16; 5 studies).

    “Subgroup analyses identified small but non-significant effects on self-reported anxiety symptoms post-treatment for cognitive and behavioural interventions (SMD -0.17; 95% CI -0.35 to 0.01; 7 studies) and relaxation (SMD -0.18; 95% CI -0.67 to 0.30; 3 studies), but observed no evidence of any effect for selfmanagement education (SMD -0.00; 95% CI -0.17 to 0.16; 5 studies).”
    Quote in the paperSubstantial claim1 of 1 sources checked
    • cites Coventry 2013 source

      Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.

      Experimental — accuracy not yet measured
  • May combine two claims.

    Premisecitation

    Coventry 2013 observed an improvement with the intervention for multi-component exercise training, though the sample included substantial heterogeneity (SMD -0.47; 95% CI -0.66 to -0.28; P = 0.002; 14 studies; I2 = 63.3%).

    “This review observed an improvement with the intervention for multi-component exercise training, though the sample included substantial heterogeneity (SMD -0.47; 95% CI -0.66 to -0.28; P = 0.002; 14 studies; I 2 = 63.3%;Coventry 2013).”
    Quote in the paperNot a substantial claim1 of 1 sources checked
    • cites Coventry 2013 source

      Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.

      Experimental — accuracy not yet measured
  • The quote only partly states this claim.

    Findingown data

    For quality of life - physical composite, the long-term follow-up SMD was -0.30 (95% CI -0.53 to -0.06; P = 0.01).

    “long-term follow-up (6 to 12 months; SMD -0.30, 95% CI -0.53 to -0.06; P = 0.01)”
    Quote in the paperSubstantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). The quote only partly states this claim.

    Findingown data

    The quality of life - physical composite analysis included 289 participants from 2 studies.

    “289 (2 studies)”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingown data

    The mean quality of life - emotional composite in the control groups was 52.3.

    “The mean quality of life -emotional composite in the control groups was 52. 3”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingnone given

    The mean exercise capacity in the control groups was 839.

    “The mean exercise capacity in the control groups was 839”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Findingcitation

    The Kunik 2008 study examined 6MWD at 8 weeks (post-intervention) and again at 12 months' follow-up with a difference in favour of the control arm at 12 months (P = 0.05).

    “The Kunik 2008 study which examined 6MWD at 8 weeks (post-intervention) and again at 12 months' follow-up with a difference in favour of the control arm at 12 months (P = 0.05).”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Kunik 2008 source
  • May combine two claims.

    Findingcitation

    Authors reported that group means at beginning of the follow-up period were not equal (P < 0.01), contributing to the spurious finding.

    “However, authors reported that group means at beginning of the follow-up period were not equal (P < 0.01), contributing to the spurious finding.”
    Quote in the paperSubstantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). The quote only partly states this claim.

    Findingown data

    The quality of life - emotional composite analysis included 289 participants from 2 studies.

    “289 (2 studies)”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Findingown data

    Two studies reported on quality of life, with one study (Kunik 2008) reporting both SF36 and CRQ.

    “Two studies reported on quality of life with one study (Kunik 2008) reporting both SF36 and CRQ.”
    • Also stated in: § Quality of life -emotional composite SGRQ and SF36 Follow-up: 6-12 months · plain
      “Two studies reported on quality of life with one study (Kunik 2008) reporting both SF36 and CRQ.”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Kunik 2008 source
  • May combine two claims.

    Findingown data

    Only one study (Kunik 2008) reported dyspnoea via CRQ, with an improvement in the CBT group over control at eight-week end-of-treatment follow-up (intervention mean 3.36 + 1.64; control mean 3.51 + 1.59; P = 0.02).

    “Only one study (Kunik 2008) reported dyspnoea via CRQ, with an improvement in the CBT group over that of control at eight-week end-of-treatment follow-up (intervention group mean 3.36 + 1.64; control group mean 3.51 + 1.59; P = 0.02).”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Findingown data

    Substantial heterogeneity was identified in all meta-analyses across studies, suggesting the possibility of true differences in the underlying treatment effect.

    “Substantial heterogeneity was identified in all meta-analyses across studies, suggesting the possibility of these being true differences in the underlying treatment effect.”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Findingown data

    There was substantial heterogeneity (I2 = 62%) in the anxiety meta-analysis, which limits the reliability of the findings.

    “However, there was substantial heterogeneity (I 2 = 62%), which limits the reliability of the findings.”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Findingown data

    Each included study reported difficulties with sample size, with two unable to meet target recruitment and the third not reporting a prespecified sample size calculation.

    “Each study reported difficulties with sample size, two being unable to meet the target recruitment number (Kunik 2008;Hynninen 2010) and the third (de Godoy 2003) not reporting a prespecified sample size calculation.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Findingown data

    Sample sizes ranged from n = 30 in de Godoy 2003, n = 51 in Hynninen 2010, and n = 238 in Kunik 2008.

    “Samples sizes ranged from n = 30 in de Godoy 2003, n = 51 in Hynninen 2010 and the largest being n = 238 in Kunik 2008.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingnone given

    The majority of participants in this review were men.

    “Also important to note is that the majority of the participants of this review were men.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Findingcitation

    No studies provided data specifically on length of stay or hospital readmission rates; the Kunik 2008 study indirectly examined this and found no differences between groups in the ratio of pre-treatment to post-treatment outpatient visits, hospital admissions, mental health visits and emergency visits per month per participant.

    “No studies provided data specifically on length of stay or hospital readmission rates.However the Kunik 2008 study did indirectly examine this by tracking the number of treatment visits pre and post study.No differences were observed for the ratio of pre treatment to post treatment between groups for outpatient visits, hospital admissions, mental health visits and emergency visits per month, per”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Findingown data

    Seven studies were awaiting classification and two were ongoing at the time of review completion.

    “Seven studies are awaiting classification and two were ongoing at the time of review completion (Figure 1).”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Findingown data

    For anxiety, short-term (0 to 3 month follow-up) benefits favoured the intervention arm (MD -3.86; 95% CI -6.63 to -1.10; P = 0.006; I2 = 19%), while these findings were not maintained long-term (6 to 12 months; MD -4.30; 95% CI -10.57 to 1.97; P = 0.18; I2 = 80%).

    “In the case of anxiety, short-term (0 to 3 month follow-up) benefits were seen in favour of the intervention arm with a MD of -3.86; 95% CI of -6.63 to -1.10 and P = 0.006 (I 2 = 19%), whilst these findings were not maintained long-term (6 to 12 months; MD -4.30 with 95% CI of -10.57 to 1.97 and P = 0.18; I 2 = 80%; Analysis 2.1).”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Findingown data

    The quality of evidence in this review overall was low, with two of the three studies having prespecified protocols available for comparison to methods and outcomes reported in the final publications.

    “The quality of evidence in this review overall was low, with two of the three studies having prespecified protocols available for comparison to methods, and outcomes reported on within the final publications.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingown data

    Thirteen potentially eligible studies (15 full-text articles) were excluded from the review.

    “We excluded 13 of the potentially eligible studies (15 full-text articles) from the review due to no diagnosis of anxiety at baseline”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Findingnone given

    All three included studies measured anxiety using the Beck Anxiety Inventory (BAI).

    “All three studies measured anxiety using the Beck Anxiety Inventory (BAI).”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Findingnone given

    All three included studies were single-centre, parallel RCTs from Brazil, Norway and the USA.

    “All three studies were single-centre, parallel RCTs coming from Brazil (de Godoy 2003), Norway (Hynninen 2010) and the USA (Kunik 2008).”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Findingown data

    In the Kunik 2008 study, of 256 eligible participants, 238 were randomised but only 181 attended their first session, a 24% attrition before the intervention commenced.

    “Of the 256 eligible participants for the Kunik 2008 study, 238 were randomised but only 181 attended their first session (24% attrition before the intervention commenced).”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Findingnone given

    All three included studies recruited participants with both anxiety and depression, not just anxiety, and compared psychotherapy with co-intervention versus co-intervention alone.

    “All three included studies recruited participants with both anxiety and depression, not just anxiety (which may confound the results) and compared psychotherapy with co-intervention versus co-intervention alone.”
    Quote in the paperSubstantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    Anxiety can occur at any stage of COPD.

    “Other studies suggest that anxiety can occur at any stage of COPD (Kim 2000;Heslop-Marshall 2014.”
    Quote in the paperNot a substantial claim0 of 2 sources checked
    • cites Kim 2000 source
    • cites Heslop-Marshall 2014

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

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

    Premisecitation

    The lifetime prevalence of GAD amongst people with COPD is estimated at between 10% and 15.8%.

    “The lifetime prevalence of GAD in particular amongst people with COPD is estimated at between 10% and 15.8% (Brenes 2003).”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Brenes 2003 source
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Premisecitation

    Rates of anxiety symptoms in people with COPD range from 13% to 51% and are higher than the rates in people with heart failure, cancer, and other medical conditions.

    “Rates of anxiety symptoms in people with COPD range from 13% to 51% and are higher than the rates in people with heart failure, cancer, and other medical conditions (Brenes 2003).”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Brenes 2003 source
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    The prevalence of panic disorder in the COPD population is estimated to be ten times higher than the general population.

    “The prevalence of panic disorder in the COPD population is estimated to be ten times higher than the general population (Smoller 1996;Smoler 1999).”
    Quote in the paperNot a substantial claim0 of 2 sources checked
    • cites Smoller 1996 source
    • cites Smoler 1999

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

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

    Premisecitation

    One model explains increased levels of anxiety and panic in people with COPD as catastrophic misinterpretations of ambiguous bodily sensations (such as shortness of breath, rapid heart rate) which increase arousal, creating a positive feedback loop that results in a panic attack.

    “One model explains this relationship as catastrophic misinterpretations of ambiguous bodily sensations (such as shortness of breath, rapid heart rate) which increase arousal, creating a positive feedback loop that results in a panic attack (Clark 1986).”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Clark 1986 source
  • May combine two claims.

    Premisecitation

    Current evidence examining quality of life suggests a reduction in satisfaction above and beyond what should be expected by COPD disease severity or co-morbid medical illnesses, indicating that psychological status plays an intrinsic role in overall well-being.

    “Current evidence examining quality of life suggests a reduction in satisfaction above and beyond what should be expected by COPD disease severity or co-morbid medical illnesses (Coventry 2007), indicating that psychological status plays an intrinsic role in overall well-being.”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites Coventry 2007 source
  • May combine two claims.

    Premisecitation

    Dyspnoea is an ambiguous sensation open to catastrophic interpretation, leading to increased levels of anxiety and panic in people with COPD.

    “Dyspnoea (shortness of breath) can be an unpleasant and potentially frightening experience at any time, and, as the key symptom of an eventually fatal illness like COPD, it is an ambiguous sensation open to catastrophic interpretation, leading to increased levels of anxiety and panic in people with COPD (Livermore 2010b).”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites Livermore 2010b

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

  • May combine two claims.

    Premisecitation

    A recent study found that people with COPD and anxiety felt isolated and would avoid social occasions and usual daily activities.

    “A recent study examining the impact of anxiety on the lives of people with COPD found that they felt isolated and would avoid social occasions and usual daily activities (Willgoss 2011).”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites Willgoss 2011

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

  • May combine two claims.

    Premisecitation

    The evidence for treatment of anxiety disorders in COPD is limited, and there are limited data to support the efficacy of medication-only treatments.

    “The evidence for treatment of anxiety disorders in COPD is limited, and there are limited data to support the efficacy of medicationonly treatments (Borson 1998).”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites Borson 1998

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

  • May combine two claims.

    Premisecitation

    Anxiety is common in COPD and is not correlated with COPD severity.

    “Screening data from a large randomised controlled trial in the UK showed anxiety was common in COPD and was not correlated with COPD severity (Heslop-Marshall 2014).”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites Heslop-Marshall 2014

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

  • May combine two claims.

    Premisecitation

    Anxiety disorders in people with COPD increase disability and impair functional status, resulting in an overall reduction in their quality of life.

    “Anxiety disorders in people with COPD have been shown to increase disability and impair functional status, resulting in an overall reduction in their quality of life (Beck 1988;Weaver 1997).”
    Quote in the paperSubstantial claim0 of 2 sources checked
    • cites Beck 1988 source
    • cites Weaver 1997 source
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    Two of three review authors retrieved and independently examined the full texts of studies identified as potentially relevant for final inclusion.

    “Two of three review authors, as above, retrieved and independently examined the full texts of studies identified as potentially relevant for final inclusion.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    Two independent review authors extracted data using a standardised and piloted data extraction form.

    “Two independent review authors (a combination of ZU, KC and KHM) extracted the following data using a standardised and piloted data extraction form, for each included study.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    Two of three review authors independently assessed all citations generated from the search strategies to determine whether they satisfied the inclusion criteria.

    “Two of three review authors (either KC, ZU or KHM) independently assessed all citations generated from the search strategies to determine whether they satisfied the Criteria for considering studies for this review, through screening of the title, abstract and descriptors.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductcitation

    Two review authors independently assessed the risk of bias for all included studies using the Cochrane tool for assessing risk of bias.

    “Two review authors independently assessed the risk of bias for all the included studies using the Cochrane tool for assessing risk of bias, which is a domain-based evaluation (Higgins 2011a).”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Higgins 2011a

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

  • May combine two claims.

    Interpretationown data

    Some evidence of improvement in anxiety was observed favouring the psychological therapy arm, but substantial heterogeneity and low quality of evidence limit the reliability of these findings.

    “Some evidence of improvement in anxiety was observed with a benefit in favour of the psychological therapy arm, however, the presence of substantial heterogeneity and low quality of the evidence limits the reliability of these findings.”
    Quote in the paperSubstantial claim
  • Classified as probably not a substantial claim.

    Study design and conductreasoning

    We extracted data from cross-over studies for the first phase only (pre-cross-over), due to the potential for a significant carry-over effect for psychological therapies.

    “We extracted data from cross-over studies for the first phase only (pre-cross-over), due to the potential for a significant carry-over effect for psychological therapies.”
    Quote in the paperSubstantial claim
  • Classified as probably not a substantial claim.

    Study design and conductcitation

    For cluster-randomised studies, we performed analyses at the level of individuals, whilst accounting for the clustering in the data using a random-effects model for pooled meta-analysis.

    “For cluster-randomised studies, we performed analyses at the level of individuals, whilst accounting for the clustering in the data using a random-effects model for pooled meta-analysis, as recommended in the Cochrane Handbook for Systematic Reviews of Interventions (chapter 16.3.3) (Higgins 2011b) (checked by a statistician (AE)).”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites Higgins 2011b

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

  • May combine two claims.

    Study design and conductown data

    Two included studies sufficiently reported allocation concealment, using an external statistician (Kunik 2008) and numbered identical containers (Hynninen 2010).

    “Two studies sufficiently reported allocation concealment using an external statistician to provide treatment codes to the study coordinator once sufficient numbers of participants for two classes had been recruited (Kunik 2008) and by using numbered containers that were identical in appearance for the two groups (Hynninen 2010).”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductnone given

    The de Godoy 2003 study did not report any details of allocation concealment.

    “The de Godoy 2003 study did not report any details of allocation concealment.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Study design and conductown data

    The two remaining included studies reported randomisation as occurring but did not describe their methods in detail.

    “The two remaining studies reported randomisation as occurring, however, they did not describe their methods in detail.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Study design and conductown data

    Selective reporting was a low risk in two included studies due to available prespecified protocols, while de Godoy 2003 had unclear risk because no prespecified protocol could be reviewed.

    “Selective reporting was a low risk in two studies due to the availability of prespecified published protocols, allowing adequate comparison of prespecified outcomes and those reported in the publications.We assessed the de Godoy 2003 study as having an unclear risk of bias due to the inability to review a prespecified protocol.”
    Quote in the paperNot a substantial claim
  • Classified as probably not a substantial claim.

    Study design and conductcitation

    For studies that did not adjust for clustering, we replaced the actual sample size with the effective sample size (ESS), calculated using a rho = 0.02.

    “For those studies that did not adjust for clustering, we replaced the actual sample size with the effective sample size (ESS), calculated using a rho = 0.02 (as per Campbell 2000).”
    Quote in the paperSubstantial claim0 of 1 sources checked
    • cites Campbell 2000

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

  • May combine two claims.

    Interpretationreasoning

    The identification of six ongoing studies and one awaiting classification is reassuring, but there is a possibility of negative studies being missed before publication of protocols became mandatory.

    “The identification of six ongoing studies and one awaiting classification is reassuring, however, there is the possibility of negative studies being missed before publication of protocols became mandatory.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Study design and conductown data

    Outcome assessor blinding was unclear in two included studies and was assessed as low risk of bias in Kunik 2008.

    “Outcome assessor blinding was unclear in two studies and assessed to be a low risk of bias in the Kunik 2008 study as authors reported that study personnel performing assessments were blinded to treatment condition.”
    Quote in the paperNot a substantial claim
  • Classified as probably not a substantial claim.

    Study design and conductnone given

    For participants who dropped out after the second week or with unclear dropout time, we used the last observation carried forward (LOCF) as presented in the publications.

    “For participants who dropped out a er the second week or with unclear dropout time, we used the last observation carried forward (LOCF) as presented in the publications, or had the data been missing we would have obtained raw data.”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Study design and conductown data

    Two included studies did not blind participants or personnel to treatment allocation, while de Godoy 2003 reported that group 1 was blinded in relation to the activities of group 2 and vice versa.

    “Two studies did not blind participants or personnel to the treatment allocation, whilst the third study (de Godoy 2003) reported that group 1 was blinded in relation to the activities of group 2 and vice versa.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductcitation

    We evaluated missing information regarding participants on an available case-analysis basis.

    “We evaluated missing information regarding participants on an available case-analysis basis as described in chapter 16.2.2 of the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011b).”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Higgins 2011b

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

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

    Interpretationreasoning

    Findings from this review should be interpreted with caution and the questions posed in this review remain unanswered.

    “As such, findings from this review should be interpreted with caution and the questions posed in this review remain unanswered.”
    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 conductnone given

    We performed a sensitivity analysis for studies which were at an unclear or high risk of bias for sequence generation and allocation concealment, and for studies involving participants who had significant co-morbidities.

    “We assessed all the included studies for inclusion in the primary analyses, and performed a sensitivity analysis for studies which were at an unclear or high risk of bias for sequence generation and allocation concealment, and for studies involving participants who had significant co-morbidities, for example, dementia or severe heart failure.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Interpretationreasoning

    Because only three studies were included, it is difficult to examine consistency effectively, and the quality of results was downgraded due to inconsistency.

    “However, as we only included three studies, it is difficult effectively to examine consistency.As such, the quality of results was downgraded due to inconsistency.”
    Quote in the paperSubstantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.

    Interpretationnone given

    Screening of online clinical trial registries allows identification of studies regardless of a positive or negative effect, which may reduce the possibility of publication bias.

    “Screening of online clinical trial registries allows identification of studies regardless of a positive or negative effect for the treatment, which may reduce the possibility of publication bias.”
    Quote in the paperNot a substantial claim
  • May combine two claims.

    Study design and conductreasoning

    All three included studies had a low risk of bias for incomplete outcome data because they used intention-to-treat analyses.

    “All three studies had a low risk of bias for incomplete outcome data as they used intention-to-treat analyses.”
    Quote in the paperNot a substantial claim
  • Classified as probably not a substantial claim.

    Study design and conductreasoning

    We pooled the extracted data in meta-analyses using the random-effects model to allow for expected heterogeneity.

    “We pooled the extracted data in meta-analyses using the randomeffects model to allow for expected heterogeneity (due to expected differences in the interventions and populations).”
    Quote in the paperSubstantial claim
  • May combine two claims.

    Premisecitation

    Meta-analyses attempting to examine the impact of psychological interventions for anxiety in people with COPD have consistently identified a lack of methodologically rigorous evidence to support treatment efficacy, resulting in the inability to draw reliable conclusions.

    “Meta-analyses attempting to examine the impact of psychological interventions for anxiety in people with COPD have consistently identified a lack of methodologically rigorous evidence to support treatment efficacy (Rose 2002;Mikkelsen 2004;Baraniak 2011), resulting in the inability to draw reliable conclusions.”
    Quote in the paperSubstantial claim0 of 3 sources checked
    • cites Rose 2002 source
    • cites Mikkelsen 2004 source
    • cites Baraniak 2011 source
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Premisecitation

    A 2014 overview examining the prevalence, impact and management of depression and anxiety in COPD found that the quality of evidence underpinning treatment varied considerably.

    “A 2014 overview examining the prevalence, impact and management of depression and anxiety in COPD also found that the quality of evidence underpinning treatment varied considerably (Panagioti 2014).”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Panagioti 2014

      Couldn’t be matched to a paper in Crossref, so it can’t be checked.

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

    Study design and conductreasoning

    An additional limitation is that risk of bias categories were deemed unclear by review authors because individual study authors were not contacted for clarification or further information.

    “An additional limitation relates to risk of bias categories deemed to be unclear by review authors, as we did not contact individual study authors for clarification or to obtain further information.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductcitation

    In Hynninen 2010, random sequence generation was at unclear risk of selection bias because randomisation was reported but methods were not described.

    “Random sequence generation (selection bias) Unclear risk Randomisation reported however methods not described”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Hynninen 2010 source
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductcitation

    In Hynninen 2010, allocation concealment was at low risk of selection bias because numbered containers identical in appearance were used.

    “Allocation concealment (selection bias) Low risk Allocation concealment was implemented using numbered containers that were identical in appearance for the two groups”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Hynninen 2010 source
  • May combine two claims.

    Interpretationown data

    Some evidence of improvement in anxiety was observed in the psychological therapy arm, but the low quality of evidence and substantial heterogeneity limit the ability to draw conclusions from these findings.

    “Some evidence of improvement in anxiety was observed in the psychological therapy arm, however, the low quality of the evidence and presence of substantial heterogeneity limits our ability to draw any conclusions from these findings.”
    Quote in the paperSubstantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    For Kunik 2008, allocation concealment was at low risk of selection bias.

    “Allocation concealment (selection bias) Low risk The statistician provided randomisation numbers and treatment codes to the study co-ordinator when sufficient participants for two classes had completed the baseline assessment and consented to participate; the instructor assigned the treatment to the code initially by flipping a coin”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductreasoning

    For Kunik 2008, selective reporting was at low risk of reporting bias.

    “Selective reporting (reporting bias) Low risk Pre-specified protocol available and no selective reporting identified”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    For de Godoy 2003, incomplete outcome data was at low risk of attrition bias.

    “Incomplete outcome data (attrition bias) All outcomes Low risk Reasons for choosing not to participate prior to randomisation (n = 6 participants) and attrition post recruitment (n = 3 intervention participants) were reported for all participants”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    Sensitivity analyses were not conducted because the number of included studies in each meta-analysis was small.

    “We did not conduct sensitivity analyses due to the small number of included studies reported within each meta-analysis.”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    For de Godoy 2003, blinding of outcome assessment was at unclear risk of detection bias.

    “Blinding of outcome assessment (detection bias) All outcomes Unclear risk No mention of blinding for outcome assessors”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    For de Godoy 2003, blinding of participants and personnel was at unclear risk of performance bias.

    “Blinding of participants and personnel (performance bias) All outcomes Unclear risk Group 1 was blinded in relation to the activities of Group 2 and vice versa”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    For Hynninen 2010, outcome measures were validated, with the exception of service use outcomes.

    “Outcome measures validated?: yes, with the exception of service use outcomes”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    For de Godoy 2003, selective reporting was at unclear risk of reporting bias.

    “Selective reporting (reporting bias) Unclear risk Insuffient information due to lack of prespecified study protocol”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductcitation

    In Hynninen 2010, the target sample size from the power analysis (33 per arm) was not reached (25 in the intervention arm and 26 in the control arm).

    “the target sample size identified as being necessary in the power analysis (33 in each arm) was not reached by the end of the study period (25 in the intervention arm and 26 in the control arm)”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Hynninen 2010 source
  • Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.

    Study design and conductown data

    For Kunik 2008, the sample size calculation required 120 participants per group, but this number was not met.

    “Also, the sample size calculation in the statistical analysis section stated that 120 participants per group would be required yet this n-value was not met”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    For Kunik 2008, blinding of participants and personnel was at high risk of performance bias.

    “Blinding of participants and personnel (performance bias) All outcomes High risk Participants and staff performing the intervention were not 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 conductown data

    For de Godoy 2003, other bias was at low risk.

    “Other bias Low risk No other biases identified”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    For Kunik 2008, other bias was at low risk.

    “Other bias Low risk No other biases identified”
    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

    For Hynninen 2010, missing data were addressed using intention-to-treat analysis, and missing data at one measurement point did not prevent including the individual in the analysis.

    “Missing data addressed?: Yes, ITT analysis used and authors reported that missing data at one measurement point did not prevent including the individual in the analysis”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    In Hynninen 2010, blinding of outcome assessment was at unclear risk of detection bias because there was no mention of blinding for outcome assessors.

    “Blinding of outcome assessment (detection bias) All outcomes Unclear risk No mention of blinding for outcome assessors”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Hynninen 2010 source
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    For Kunik 2008, random sequence generation was at low risk of selection bias.

    “Random sequence generation (selection bias) Low risk Randomisation list occurred via computer program (SAS) with blocks to provide appropriately equal numbers per class of COPD; instructor assigned treatment to the code initially by flip of coin”
    Quote in the paperNot a substantial claim
  • Probably not a substantial claim: may not pass S3 (load-bearing).

    Study design and conductown data

    For Kunik 2008, blinding of outcome assessment was at low risk of detection bias.

    “Blinding of outcome assessment (detection bias) All outcomes Low risk Study personnel performing assessments were blinded to 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 Hynninen 2010, there was low risk of other bias because no other biases were identified.

    “Other bias Low risk No other biases identified”
    Quote in the paperNot a substantial claim0 of 1 sources checked
    • cites Hynninen 2010 source
91 of 91

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?

  • Subject headings and free-text words were identified for use from previous systematic reviews (Hooper 2018; Uphoff 2020; Usmani 2017), the Information Specialist, and the project team members.

    “Subject headings and free-text words were identified for use from previous systematic reviews (Hooper 2018; Uphoff 2020; Usmani 2017), the Information Specialist, and the project team members.”

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.

  • Physical quality-of-life confidence interval changes sign

    Major

    The results text gives an upper confidence limit of −0.08, which would exclude no effect. The analysis table instead gives +0.08, consistent with the reported P = 0.10.

  • Walking-distance analysis uses a different model than stated

    Minor

    The methods say pooled meta-analyses used a random-effects model, but the main six-minute walking-distance analysis is labelled fixed-effect.

  • Emotional quality-of-life subgroup estimates differ

    Minor

    The summary gives short- and long-term estimates of 0.05 and −0.09; the corresponding duration analysis gives −0.17 and −0.30.

  • Physical quality-of-life subgroup estimates differ

    Minor

    The summary reports short- and long-term estimates of −0.22 and −0.30, but the corresponding duration analysis reports −0.30 and −0.40.

  • Listed dropout reasons exceed the dropout count

    Minor

    The five stated reason counts total 109, whereas the passage says 69 participants dropped out.

    Reported 69 · recomputed 109

  • Ongoing and awaiting-study counts are reversed

    Minor

    The search results assign seven studies to awaiting classification and two to ongoing status. The dedicated sections give the opposite counts.

6 of 6

Cites

Flagged first, then by citations

6 of the 97 references couldn’t be matched to a known paper.

Research works printed but not linked: 7

  1. Aubuchon, 1990, The effects of positive mental imagery on hope, coping, anxiety, dyspnea and pulmonary function in persons with chronic obstructive pulmonary disease: tests of a nursing intervention and a theoretical model [Dissertation]
  2. Shao, 2003, Effects of the behavioral intervention on the life quality of the patients with chronic obstructive pulmonary disease in remission period, Zhonghua Linchuang Kangfu Zazhi, 7, 4078
  3. Beck, 1993, Beck Anxiety Inventory: A Manual
  4. Davison, 2003, Abnormal Psychology
  5. Higgins JPT Deeks JJ (editors) Chapter 7: Selecting studies and collecting data. In: Higgins JPT, Green S (editors), Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0 (updated March 2011). The Cochrane Collaboration, 2011 Available from handbook.cochrane.org
  6. Nordic Cochrane Centre, The Cochrane Collaboration Review Manager 5 (RevMan 5) 2014
  7. Schünemann HJ Oxman AD Higgins JPT Vist GE Glasziou P Guyatt GH Chapter 11: Presenting results and ‘Summary of findings' tables. In: Higgins JPT, Green S (editors), Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0 (updated March 2011). The Cochrane Collaboration, 2011 Available from handbook.cochrane.org

Cited by

Sorted by citations

Authors
Usmani, Z. A., Carson, K. V., Heslop, K., Esterman, A. J., De Soyza, A., & Smith, B. J.
Affiliations
  • Queen Elizabeth Hospital (AU)
  • The University of Adelaide; School of Medicine; Adelaide Australia
  • Royal Victoria Infirmary (GB)
  • University of South Australia (AU)
  • Newcastle University; Institute of Cellular Medicine; Newcastle UK
  • The University of Adelaide (AU)
Venue
Cochrane Database of Systematic Reviews
Publisher
Wiley
Published
2017-03-21
Volume
2017
Issue
3
Pages
CD010673-CD010673
ISSN
  • 1361-6137 (ISSN-L)
  • 1465-1858
OpenAlex
W2140629271
Cited by
72
References
97
Citations by year
2026: 4 · 2025: 6 · 2024: 9 · 2023: 8 · 2022: 5 · 2021: 7 · 2020: 10 · 2019: 10 · 2018: 10 · 2017: 3
FWCI
1.65
Type
journal article
Language
en
Open access
Locations
  • Cochrane Database of Systematic Reviews (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • UniSA Research Outputs Repository (University of South Australia) (submittedVersion)
  • Adelaide Research & Scholarship (AR&S) (University of Adelaide) (submittedVersion)
  • Newcastle University ePrints (Newcastle Univesity)
Funders
  • National Institute for Health and Care Research (CAT CDRF 10-023)
  • University of Aberdeen
  • National Institutes of Health
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
  • Social Sciences › Psychology › Experimental and Cognitive Psychology › Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Health and Mental Health
Keywords
chronic obstructive pulmonary disease, anxiety disorders, psychotherapy, cognitive behavioral therapy, relaxation training, breathing exercises, COPD exacerbations, quality of life, dyspnea, exercise tolerance, treatment efficacy, adverse events, cost-effectiveness, cost-benefit analysis, cost-effectiveness ratio, benefit-cost ratio
MeSH terms
Anxiety Disorders, Emphysema, Female, Humans, Male, Psychotherapy, Quality of Life, Randomized Controlled Trials as Topic, Exercise Tolerance, Pulmonary Disease, Chronic Obstructive, Bronchitis, Chronic

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 2026-10-11.

Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-11.

Cited sources are checked by gpt-6-sol.

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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