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. 2016 Mar 2;2016(3):CD008378. doi: 10.1002/14651858.CD008378.pub3

Summary of findings 2. Lively Legs programme compared with wounds outpatient clinic.

Lively Legs programme versus outpatient wound clinic
Patient or population: people with venous leg ulcers
 Settings: community
 Intervention: Lively Legs programme
Comparison: wounds outpatient clinic
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No of Participants
 (studies) Quality of the evidence
 (GRADE) Comments
Assumed risk Corresponding risk
Control Lively Legs programme versus outpatient wound clinic
Time to healing ‐ not reported See comment See comment Not estimable See comment Not reported
Number of people healed 
 Follow‐up: 18 months 45 per 100 55 per 100 
 (41 to 74) RR 1.24 
 (0.93 to 1.67) 184
 (1 study) ⊕⊕⊝⊝
 low1,2  
Adverse events ‐ not reported See comment See comment Not estimable See comment Adverse events were not reported, unclear if measured
Recurrence of ulcers 
 Follow‐up: 18 months 57 per 100 47 per 100 
 (33 to 65) RR 0.82 
 (0.59 to 1.14) 136
 (1 study) ⊕⊕⊝⊝
 low1,2  
Quality of life ‐ not reported See comment See comment Not estimable See comment Not reported
Adherence to compression 
 Follow‐up: 18 months 45 per 100 45 per 100 
 (31 to 66) RR 1.02 
 (0.74 to 1.41) 184
 (1 study) ⊕⊕⊝⊝
 low1,2  
Pain ‐ not measured See comment See comment Not estimable See comment Not measured
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. 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; RR: risk ratio
GRADE Working Group grades of evidence
 High quality: further research is very unlikely to change our confidence in the estimate of effect.
 Moderate quality: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
 Low quality: 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: we are very uncertain about the estimate.

1 Trialists failed to report randomisation method and allocation concealment
 2 Low number of participants; 95% confidence interval includes both no effect and appreciable benefit