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. 2012 Nov 14;2012(11):CD007407. doi: 10.1002/14651858.CD007407.pub3

Williams 1996.

Methods RCT; 3 arms; assessed at pre‐treatment, post‐treatment, 6 months, 1 year
Participants End of treatment n = 99
Start of treatment n = 121
Sex: 68 F, 53 M
Mean age = 50.0 (SD 11.5)
Source = pain clinic
Diagnosis = mixed chronic pain, low back commonest
Mean years of pain = 7.8
Interventions "inpatient CBT"
"outpatient CBT"
"waiting list"
Outcomes Primary pain outcome: VAS pain
Primary disability outcome: SIP patient‐rated
Primary mood outcome: BDI depression
Catastrophising outcome: CSQ catastrophising
Visual analogue scale (VAS): pain intensity
Visual analogue scale (VAS): pain distress
Sickness Impact Profile (SIP): patient‐rated
Beck Depression Inventory (BDI)
State‐Trait Anxiety Inventory (STAI)
Coping Strategies Questionnaire (CSQ): catastrophising
Pain Self‐Efficacy Questionnaire (PSEQ)
Pain Cognitions Questionnaire (PCQ)          
Walk distance                    
Arm endurance                      
Stair climb                        
Stand ups
Medication use
Health care use                          
Notes CBT versus TAU, post‐treatment (waiting list not followed up): analyses 3.1, 3.2, 3.3
Yates quality scale: total quality = 22/35, design quality = 15/26, treatment quality = 7/9
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk “Randomly assigned by throw of a die”
Allocation concealment (selection bias) High risk Not reported
Incomplete outcome data (attrition bias) 
 All outcomes Low risk Attrition reported
Selective reporting (reporting bias) High risk Partially reported
Blinding of outcome assessment (detection bias) 
 All outcomes Low risk “interviewers and assistants blind to the patients’ treatment”