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. 2014 Nov 1;2014(11):CD011142. doi: 10.1002/14651858.CD011142.pub2

Summary of findings 2. Psychological therapy compared with enhanced or structured care for somatoform disorders and medically unexplained physical symptoms.

 
Patient or population: somatoform disorders and medically unexplained physical symptoms
 Settings: all settings
 Intervention: psychological therapies
 Comparison: enhanced or structured care
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No of participants
 (studies) Quality of the evidence
 (GRADE) Comments
Assumed risk Corresponding risk
Enhanced or structured care Psychological therapies
Severity of somatic symptoms at end of treatment The mean severity of somatic symptoms at end of treatment in the intervention groups was
 0.19 standard deviations lower 
 (0.43 lower to 0.04 higher) 624
 (5 studies1) ⊕⊕⊕⊝
 low2, 11 95% CI excluded large effect (> 0.5 SMD)
Acceptability 
 1 ‐ proportion of participants withdrawing during treatment 904 per 1000 841 per 1000 
 (787 to 904) RR 0.93 
 (0.87 to 1) 679
 (5 studies3) ⊕⊕⊕⊝
 moderate4
Dysfunctional cognitions, emotions, or behaviours at end of treatment 
 Whitely Index (different forms) The mean dysfunctional cognitions, emotions, or behaviours at end of treatment in the intervention groups was
 0.09 standard deviations lower 
 (0.29 lower to 0.1 higher) 499
 (4 studies5) ⊕⊕⊕⊝
 moderate6 95% CI excluded clinically relevant effect
Treatment response at end of treatment Study population Not estimable 0
 (0) See comment No studies reported on this outcome (see text)
See comment See comment
Moderate
Functional disability/quality of life at end of treatment 
 Various instruments The mean functional disability/quality of life at end of treatment in the intervention groups was
 0.13 standard deviations higher 
 (0.05 lower to 0.3 higher) 497
 (4 studies7) ⊕⊕⊕⊝
 moderate6 95% CI excluded clinically relevant effect
Healthcare use within 1 year after treatment The mean healthcare use within 1 year after treatment in the intervention groups was
 0.24 standard deviations lower 
 (0.46 to 0.01 lower) 319
 (2 studies8) ⊕⊕⊝⊝
 low9,10
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
 CI: confidence interval; RR: risk ratio; SMD: standardised mean difference.
GRADE Working Group grades of evidence
 High quality: Further research is very unlikely to change our confidence in the estimate of effect.
 Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
 Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
 Very low quality: We are very uncertain about the estimate.

1 Analysis 2.1.
 2 I2 = 53%
 3 Analysis 2.4.
 4 Quality of evidence downgraded by one point as studies not blinded. As acceptability and loss to follow‐up are interrelated, we decided not to downgrade the evidence for loss to follow‐up.
 5 Analysis 2.8.
 6 Assessment of quality of evidence downgraded by one point as studies were not blinded.
 7 Analysis 2.11.
 8 Analysis 2.15.
 9 In addition to both studies not being blinded, high loss to follow‐up in one study. We therefore downgraded our assessment of the quality of the evidence by two points.
 10 Only 2 studies with < 400 analysed participants.

11 No blinding (all studies) and >20% loss to follow up (2 studies)