Sjögren 2005.
Methods | RCT; cluster‐randomised, cross‐over trial; four clusters | |
Participants | Office workers with headache, neck or shoulder pain; n = 53 | |
Interventions |
I: Physical exercise: progressive light resistance training and guidance; n = 36 C: No intervention: n = 17 Treatment period: 15 weeks; cross‐over at 15 weeks |
|
Outcomes | Pain (Borg CR10 Scale), strength | |
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Cluster‐randomisation, but method of randomisation not specified |
Allocation concealment (selection bias) | Low risk | "Blind measurers allocated the workers into the two treatment sequences" |
Blinding of participants? | High risk | Participants not blinded |
Blinding of caregivers? | Unclear risk | Unclear |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Self‐reported outcomes used and participants not blinded |
Incomplete outcome data (attrition bias) All outcomes ‐ <20% drop‐outs? | Low risk | Two participants lost to follow‐up: < 20% |
Incomplete outcome data (attrition bias) All outcomes ‐ ITT analysis performed? | Low risk | Figure 1: main analysis intention‐to‐treat, none excluded from analysis |
Selective reporting (reporting bias) | Unclear risk | No protocol |
Similarity of baseline characteristics? | Low risk | Baseline comparable: see Table 1 |
Co‐interventions avoided? | Low risk | "Other physical activity performed outside the intervention was controlled by a structured interview" |
Compliance acceptable ? | Low risk | Compliance: Participants maintained a weekly diary: 78% to 68% |
Timing outcome assessment comparable? | Low risk | Timing was comparable |