Effects of (music-based) rhythmic auditory cueing training on gait and posture post-stroke: A systematic review & dose-response meta-analysis

Shashank Ghai, Ishan Ghai, Shashank Ghai, Ishan Ghai

Abstract

Gait dysfunctions are common post-stroke. Rhythmic auditory cueing has been widely used in gait rehabilitation for movement disorders. However, a consensus regarding its influence on gait and postural recovery post-stroke is still warranted. A systematic review and meta-analysis was performed to analyze the effects of auditory cueing on gait and postural stability post-stroke. Nine academic databases were searched according to PRISMA guidelines. The eligibility criteria for the studies were a) studies were randomized controlled trials or controlled clinical trials published in English, German, Hindi, Punjabi or Korean languages b) studies evaluated the effects of auditory cueing on spatiotemporal gait and/or postural stability parameters post-stroke c) studies scored ≥4 points on the PEDro scale. Out of 1,471 records, 38 studies involving 968 patients were included in this present review. The review and meta-analyses revealed beneficial effects of training with auditory cueing on gait and postural stability. A training dosage of 20-45 minutes session, for 3-5 times a week enhanced gait performance, dynamic postural stability i.e. velocity (Hedge's g: 0.73), stride length (0.58), cadence (0.75) and timed-up and go test (-0.76). This review strongly recommends the incorporation of rhythmic auditory cueing based training in gait and postural rehabilitation, post-stroke.

Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
PRISMA flow chart for the inclusion of studies.
Figure 2
Figure 2
Risk of bias across studies.
Figure 3
Figure 3
Trim and Fill funnel plot for Hedge’s g and standardized effect for each value in the meta-analysis. Each of the effect is represented in the plot as a circle. Imputed studies are represented by darkened circles. Funnel boundaries represent area where 95% of the effects are expected to lie if there were no publication biases. The vertical line represents the mean standardized effect of zero.
Figure 4
Figure 4
Forest plot illustrating individual studies evaluating the effects of rhythmic auditory cueing on gait velocity amongst post-stroke patients. Weighted effect sizes; Hedge’s g (boxes) and 95% C.I (whiskers) are presented, demonstrating repositioning errors for individual studies. The (Diamond) represents pooled effect sizes and 95% CI. A negative effect size indicated reduction in gait velocity; a positive effect size indicated enhancement in gait velocity. (CB: Cerebellum, P&M: Pons & medulla, TH: Thalamus, PU: Putamen, CR: Corona radiata, T: Treadmill).
Figure 5
Figure 5
Forest plot illustrating individual studies evaluating the effects of rhythmic auditory cueing, on stride length amongst post-stroke patients. Weighted effect sizes; Hedge’s g (boxes) and 95% C.I (whiskers) are presented, demonstrating repositioning errors for individual studies. The (Diamond) represents pooled effect sizes and 95% CI. A negative effect size indicated reduction in stride length; a positive effect size indicated enhancement in stride length. (CB: Cerebellum, P&M: Pons & medulla, TH: Thalamus, PU: Putamen, CR: Corona radiata, T: Treadmill).
Figure 6
Figure 6
Forest plot illustrating individual studies evaluating the effects of rhythmic auditory cueing, on cadence amongst post stroke patients. Weighted effect sizes; Hedge’s g (boxes) and 95% C.I (whiskers) are presented, demonstrating repositioning errors for individual studies. The (Diamond) represents pooled effect sizes and 95% CI. A negative effect size indicated reduction in cadence; a positive effect size indicated enhancement in cadence. (T: Treadmill).

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