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. 2014 Jan 23;2014(1):CD002840. doi: 10.1002/14651858.CD002840.pub3

Summary of findings for the main comparison.

Treadmill (with or without BWS) for walking after stroke

Treadmill (with or without BWS) for walking after stroke
Patient or population: patients with walking after stroke Settings: Inpatient and outpatient Intervention: Treadmill (with or without BWS)
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 Treadmill (with or without BWS)
Walking speed (m/sec) at end of treatment phase Measures of timed gait The mean walking speed (m/sec) at end of treatment phase in the control groups was 0.59 m/sec The mean walking speed (m/sec) at end of treatment phase in the intervention groups was 0.07 higher (0.03 to 0.11 higher) 1891 (35 studies) ⊕⊕⊝⊝ low1,2
Walking speed (m/sec) at end of treatment phase ‐ dependent in walking at start of treatment Measures of timed gait The mean walking speed (m/sec) at end of treatment phase ‐ dependent in walking at start of treatment in the control groups was 0.26 m/sec The mean walking speed (m/sec) at end of treatment phase ‐ dependent in walking at start of treatment in the intervention groups was 0.01 lower (0.06 lower to 0.03 higher) 752 (9 studies) ⊕⊕⊝⊝ low1,3
Walking speed (m/sec) at end of treatment phase ‐ independent in walking at start of treatment Measures of timed gait The mean walking speed (m/sec) at end of treatment phase ‐ independent in walking at start of treatment in the control groups was 0.67 m/sec The mean walking speed (m/sec) at end of treatment phase ‐ independent in walking at start of treatment in the intervention groups was 0.11 higher (0.06 to 0.16 higher) 1139 (26 studies) ⊕⊕⊕⊝ moderate1,2,4
walking endurance (m) at the end of treatment Measures of timed gait The mean walking endurance (m) at the end of treatment in the control groups was 203.7 m The mean walking endurance (m) at the end of treatment in the intervention groups was 20.08 higher (6.14 to 34.03 higher) 1388 (20 studies) ⊕⊕⊝⊝ low1,2
walking endurance (m) at the end of treatment ‐ dependent in walking at start of treatment Measures of timed gait The mean walking endurance (m) at the end of treatment ‐ dependent in walking at start of treatment in the control groups was 115.3 m The mean walking endurance (m) at the end of treatment ‐ dependent in walking at start of treatment in the intervention groups was 5.09 lower (23.41 lower to 13.22 higher) 639 (5 studies) ⊕⊕⊝⊝ low1,3
walking endurance (m) at the end of treatment ‐ independent in walking at start of treatment Measures of timed gait The mean walking endurance (m) at the end of treatment ‐ independent in walking at start of treatment in the control groups was 240.9 m The mean walking endurance (m) at the end of treatment ‐ independent in walking at start of treatment in the intervention groups was 30.61 higher (14.02 to 47.2 higher) 749 (15 studies) ⊕⊕⊕⊝ moderate1,2,4
*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;
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 Downgraded due to several ratings with "unclear" or even "high" risk of bias 2 Downgraded due to CIs embracing effect size of least clinically important benefit 3 Downgraded due to CIs embracing effect size of null hypothesis 4 Upgraded due to evidence of a dose response gradient