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Virtual reality gaming for rehabilitation of patients with urinary incontinence: a systematic review and meta-analysis |
Lialy HE, Abdalrahman HA, Elsebaie M, Abdrabo MF, Emara M, Mosad Y, Elsaid M |
Physiotherapy Research International 2024 Oct;29(4):e2112 |
systematic review |
BACKGROUND: Urinary Incontinence (UI) is a global health issue that mainly affects the female population worldwide. Different approaches have been sought for the management of UI including Pelvic floor muscle training (PFMT) using Virtual Reality (VR) gaming. We conducted this study to evaluate the effectiveness of VR gaming for rehabilitation of pelvic floor muscles (PFM) and improving urinary symptoms in patients with UI. METHOD: We've included studies that contain any type of VR in all geographic locations and settings with no restrictions on the date of publication, age, or gender. Our exclusion criteria include reviews, case series, case reports, unextractable data, unavailable full text, abstract only articles, and studies don't show the effects of VR as a treatment for UI. A pre-specified search term was used and modified according to the requirements of each of the following databases: PubMed, Web of Science, Scopus, Cochrane, Google scholar, and ScienceDirect. For risk of bias assessment, two assessment tools have been used: ROB 2.0 for RCTs and NIH for single arm studies. RESULTS: Of 915 papers identified from 6 databases, 341 papers were assigned for screening after removing duplicates, 11 papers were eligible for full text screening, and 4 papers were finally included. The qualitative analysis of the results identifies six outcomes grouped into three primary categories: PFM, urinary symptoms, and quality of life. Only urinary loss outcome was eligible for meta-analysis. The net effect between game therapy plus PFMT and PFMT reached MD -5.49, 95% CI -12.36 to 1.38 (heterogeneity; I2 95%, p < 0.01). CONCLUSION: Our research underscores the potential of VR gaming as a valuable adjunctive therapy for pelvic floor muscle rehabilitation in patients with UI. However, further studies are needed to explore its long-term effectiveness, optimal therapy parameters, and cost-effectiveness. REGISTRATION: Our protocol has been registered in PROSPERO (CRD42022384500).
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