Summary of findings 1. Implementation interventions compared with no intervention for promoting uptake of evidence‐based practices in stroke rehabilitation.
Implementation interventions compared with no intervention for promoting uptake of evidence‐based practices in stroke rehabilitation | ||||||
Patient or population: healthcare professionals providing stroke rehabilitation Settings: inpatient, outpatient or community rehabilitation Intervention: any implementation intervention Comparison: control (no intervention) | ||||||
Outcomes | Illustrative comparative risks* (95% CI) | Relative effect (95% CI) | No of participants (studies, clusters) | Quality of the evidence (GRADE) | Comments | |
Assumed risk | Corresponding risk | |||||
No intervention | Implementation intervention | |||||
Quality of care: healthcare professional adherence to EBP at 12 months | Study population stroke patients | RR 1.19 (0.53 to 2.64) | 1455 patient participants (2 trials, 39 clusters) | ⊕⊝⊝⊝ Very lowc,d | We are uncertain about the estimate of healthcare professional adherence to EBP at 12 months as the certainty of the evidence is very low. | |
5%a | 6% (2.7% to 13.2%) | |||||
33%b | 39.3% (17.5% to 87.1%) | |||||
Patient adherence to recommended treatment: number of outdoor journeys per week at 6 months | 7.4 | 7.9 (5.6 to 10.2) | Adjusted MD 0.5 (–1.8 to 2.8) | 100 participants (1 trial, 21 clusters) | ⊕⊕⊝⊝ Lowe | Implementation interventions in stroke rehabilitation may lead to little or no difference in patient adherence to recommended treatment at 6 months, compared with no intervention. |
Patient health status: HRQoL (EQ‐5D: –0.59 to 1, higher score better) at up to 6 months | 0.58f | 0.59 (0.56 to 0.63) | MD 0.01 (–0.02 to 0.05) | 1242 participants (2 trials, 65 clusters) | ⊕⊕⊕⊝ Moderateg | Implementation interventions in stroke rehabilitation probably lead to little or no difference in patient HRQoL at up to 6 months compared with no intervention. 4 trials assessed HRQoL using EQ‐5D but data from only 2 trials could be pooled. Findings across studies appeared consistent. |
Patient health status: ADL (Barthel Index, 0–20, higher score = better) at up to 6 months | 15.8f | 16.09 (15.64 to 16.53) | MD 0.29 (–0.16 to 0.73) | 1272 participants (2 trials, 65 clusters) | ⊕⊕⊕⊝ Moderateg | Implementation interventions in stroke rehabilitation probably lead to little or no difference in patient function (ADL) at up to 6 months compared with no intervention. 4 trials assessed ADL using the Barthel Index but data from only 2 trials could be pooled. Findings across studies appeared consistent. |
Patient health status: psychological well‐being (GHQ‐12, 0–36, higher score = worse) at up to 6 months | 14.9h | 14.69 (14.36 to 15.40) | SMD –0.02 (–0.54 to 0.50) | 1273 participants (2 trials, 65 clusters) | ⊕⊕⊝⊝ Lowi | Implementation interventions in stroke rehabilitation may lead to little or no difference in patient psychological well‐being at up to 6 months compared with no intervention. 3 trials reported psychological well‐being using different measures, data from 2 trials could be pooled. Findings across studies appeared consistent. |
Health professional outcomes | No studies reported this outcome | |||||
*The basis for the assumed risk (e.g. the mean 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). ADL: activities of daily living; CI: confidence interval; EBP: evidence‐based practice; EQ‐5D: EuroQol 5‐dimension health state measure; GHQ‐12: General Health Questionnaire‐12; HRQoL: health‐related quality of life; MD: mean difference; SMD: standardised mean difference; 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. |
a Adherence estimated from the control group value at 12 months in McCluskey 2016.
b Adherence estimated from the control group value at 12 months in Power 2014.
c Downgraded one level due to serious risk of bias; lack of blinding of personnel in both trials, outcome assessors not blinded and incomplete outcome data in one trial. d Downgraded two levels due to very serious imprecision; 95% confidence intervals wide. e Downgraded two levels due to very serious imprecision; suboptimal information size (one study with 100 participants) and 95% confidence intervals wide. f Estimated from the control group value at six months in Forster 2015. g Downgraded one level due to serious imprecision; suboptimal information size. h Estimated from the control group value on the GHQ‐12 at six months in Forster 2015. i Downgraded two levels due to serious indirectness; differences in outcome measures and uncertainty in whether the outcomes are assessing the same health issue.