Spence 1995.
Methods | RCT; no info on randomisation procedure | |
Participants | Chronic (> 10 months) complaints, upper extremity (non‐specific) associated with repetitive tasks in the workplace; n = 48 (40 women) | |
Interventions |
EMG biofeedback (EMG): auditory feedback on muscle tension levels + home‐based assignments; n = 12 EMG + relaxation (CO): combined treatment of EMG and ART; n = 12 Relaxation training (ART): consists of a range of relaxation techniques + home‐based assignments; n = 12 Waiting list controls (WCL): n = 12 Eight weeks. Follow‐up six months |
|
Outcomes | Pain (Whimpy, Likert, PBQ), depression (BDI), ADL | |
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Unclear randomisation procedure |
Allocation concealment (selection bias) | Unclear risk | Unclear whether allocation was concealed |
Blinding of participants? | Unclear risk | Unclear |
Blinding of caregivers? | Unclear risk | Unclear |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Unclear whether outcome assessment was blinded |
Incomplete outcome data (attrition bias) All outcomes ‐ <20% drop‐outs? | High risk | Three dropouts at short term; eight at long term (> 20%) |
Incomplete outcome data (attrition bias) All outcomes ‐ ITT analysis performed? | High risk | No ITT analysis |
Selective reporting (reporting bias) | Unclear risk | No protocol |
Similarity of baseline characteristics? | High risk | Baseline groups were regarded as not comparable |
Co‐interventions avoided? | Unclear risk | Unclear whether co‐interventions were avoided |
Compliance acceptable ? | Unclear risk | Unclear compliance |
Timing outcome assessment comparable? | Low risk | Timing was comparable |