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. 2017 Aug 3;2017(8):CD011674. doi: 10.1002/14651858.CD011674.pub2

Summary of findings 3. Back School compared with passive physiotherapy for low back pain.

Back School compared with passive physiotherapy for low back pain
Patient or population: people with low back pain.
Intervention: Back School
Comparison: passive physiotherapy
Outcomes Illustrative comparative risks (95% CI) Relative effect
 (95% CI) No of participants
 (studies) Quality of the evidence
 (GRADE)
Assumed risk Corresponding risk*
Passive physiotherapy Back School
pain: short‐term follow‐up (< 3months) 
 Multiple scales: scale from 0 to 100 (worse pain) The mean pain at short‐term follow‐up ranged across control groups from 7.1 to 88 points. The mean pain (short‐ term) in the intervention groups was 1.96 higher (9.51 lower to 13.43 higher). MD 1.96 (‐9.51 to
 13.43) 290
 participants
 (3 studies) ⊝⊝⊝⊝
 very low1,2,3,4
pain ‐ intermediate‐term follow up (3‐6 months)
Multiple scales: scale from 0 to 100 (worse pain)
The mean pain at intermediate‐term follow‐up ranged across control
 groups from 13.3 to 65 points. The mean pain (intermediate‐term) in the intervention groups was 16.89 lower (66.56 lower to 32.79 higher). MD ‐16.89 (‐66.56
 to 32.79) 290
 participants
 (3 studies) ⊝⊝⊝⊝
 very low1,2,3,4
pain ‐ long‐term follow‐up (>6 months)
Multiple scales: scale from 0 to 100 (worse pain)
The mean pain at long‐term follow‐up ranged across control groups from 11.6 to 60.5 points. The mean pain (long‐ term) in the intervention groups was 12.86 lower (61.22 lower to 35.50 higher). MD ‐12.86 (‐61.22
 to 35.50) 291
 participants
 (3 studies) ⊝⊝⊝⊝
 very low1,2,3,4
Disability ‐ short‐term follow‐up (<3 months)
Multiple scales:
 scale from 0 to 100
 (worse disability)
The mean disability at short‐term follow‐up ranged across control groups from 9.1 to 60 points. The mean disability at short‐term follow‐up in the intervention groups was 2.57 higher (15.88 lower to 21.01 higher). MD 2.57
 (‐15.88 to
 21.01) 180
 participants
 (2 studies) ⊝⊝⊝⊝
 very low1,2,3,4
Disability ‐ intermediate‐term follow up (3‐6 months)
Multiple scales:
 scale from 0 to 100
 (worse disability)
The mean disability at intermediate‐term follow‐up
 ranged across control groups from 10.4 to 53 points. The mean disability at short‐term follow‐up in the intervention groups was 6.88 higher (‐4.86 lower to 18.63 higher). MD 6.88
 (‐4.86 to
 18.63). 180
 participants
 (2 studies) ⊕⊝⊝⊝
 very low1,2,4
Disability ‐ long‐term follow‐up (>6 months)
Multiple scales:
 scale from 0 to 100
 (worse disability)
The mean disability at long‐term follow‐up ranged across
 control groups from 10.4 to 46 points. The mean disability at long‐term follow‐up in the intervention groups was 9.60 higher (3.65 higher to 15.54 higher). MD 9.60
 (3.65 to 15.54) 180
 participants
 (2 studies) ⊕⊝⊝⊝
 very low1,2,4
Adverse events Not reported
Work status Not reported
The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; MD: mean difference
GRADE Working Group grades of evidence
High‐quality evidence: There are consistent findings among at least 75% of randomised controlled trials with low risk of bias; consistent, direct, and precise data; and no known or suspected publication biases. Further research is unlikely to change either the estimate or our confidence in the results.
Moderate‐quality evidence: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
 Low‐quality evidence: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
 Very low‐quality evidence: We are very uncertain about the results.
 No evidence: We identified no randomised controlled trials that addressed this outcome.

1 Downgraded one level due to imprecision (fewer than 400 participants, in total).
 2 Downgraded one level due to risk of bias (> 25% of the participants were from studies with a high risk of bias).
 3 Downgraded one level due to clear inconsistency of results.
 4 Downgraded one level due to publication bias.