Ketola 2002.
Methods | RCT; no info on randomisation procedure; ‘care‐giver’ blinded | |
Participants | Employees working with video display units (VDUs). Neck/shoulder complaint > one month; non‐specific; n = 124. Employees who use the mouse currently | |
Interventions |
Intensive ergonomics: two physiotherapists visited the worksite and changed worksite according to checklist; n = 39 Education ergonomics: workers attended a one‐hour training session in ergonomics; n = 35 Control group: one‐page leaflet; n = 35 Two‐ and 10‐month follow‐up |
|
Outcomes | Discomfort (6‐point Likert), strain (6‐point Likert), pain (yes/no) | |
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | "Using stratified random sampling—The three administrational units were used as a stratum. The success of the randomization was checked.." |
Allocation concealment (selection bias) | Unclear risk | Unclear whether allocation was concealed |
Blinding of participants? | Unclear risk | Participants unclear whether blinded |
Blinding of caregivers? | Unclear risk | Unclear whether care provider blinded |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Two blinded experts used to detect changes in workstations, but diary and questionnaires provided self‐reported outcomes; participants not fully blinded |
Incomplete outcome data (attrition bias) All outcomes ‐ <20% drop‐outs? | Low risk | Seven dropouts: < 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? | Low risk | Groups similar at baseline |
Co‐interventions avoided? | Unclear risk | Unclear whether co‐interventions were avoided |
Compliance acceptable ? | Unclear risk | Unclear compliance rate |
Timing outcome assessment comparable? | Low risk | Timing comparable |