Glombiewski 2010b.
Methods | RCT; 3 arms: CBT + biofeedback; CBT; waiting list control, post‐treatment (WLC assigned to treatment so no WLC at 6‐month follow‐up) | |
Participants | End of treatment: n = 116 Start of treatment: n = 128 Sex: 77 F, 39 M Mean age: 48.8 (SD 11.7) Source = medical referrals (86%) or response to newspaper advert (14%) Diagnosis = chronic back pain Mean years of pain: 8.1 (SD 8.7) |
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Interventions | "CBT with biofeedback" "CBT" "waiting list control" |
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Outcomes |
Primary pain outcome: 0 to 10 NRS pain intensity Primary disability outcome: PDI Primary mood outcome: BDI Catastrophising outcome: none Pain intensity 0 to 10 NRS Pain average of 4x daily diary for 1 week Pain Disability Index Beck Depression Inventory Coping Strategies Scale from FESV Health‐Related Life Satisfaction Scale Global treatment change Treatment satisfaction (Adverse events noted from pain intensity and global treatment change) Health care use: doctor visits for pain |
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Notes | Combined (CBT + biofeedback and CBT) versus WLC: analyses 3.1, 3.2, 3.3 2011 update search Yates quality scale: total quality 24/35, design quality 17/26, design quality 15/26 |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Randomisation by random number generation |
Allocation concealment (selection bias) | Unclear risk | “coordinated by the first author” before study |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Attrition fully reported; statement that dropout data will be reported elsewhere |
Selective reporting (reporting bias) | Low risk | Fully reported |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Not reported |