Randomized Controlled Non-Inferiority Trial Comparing a Mobile Application Based Program With Conventional Rehabilitation for Stress and Mixed Urinary Incontinence in Adult Women
The goal of this clinical trial is to learn if a mobile app-guided pelvic floor rehabilitation program works as well as standard in-person pelvic floor rehabilitation to treat urinary leakage in adult women. The main question it aims to answer is: Does the app program improve quality of life related to urinary leakage as much as in-person rehabilitation? Researchers will compare the app-based program to in-person rehabilitation to see if both lead to similar improvements in quality of life. Participants will: Attend one medical visit before starting to confirm they are eligible Attend one in-person training session with a physiotherapist Follow either an app-based or an in-person pelvic floor rehabilitation program for 3 months Complete quality of life questionnaires at the start and at 4 months
• age \>18 years
• stress urinary incontinence (SUI) or mixed urinary incontinence with predominance of SUI
• more than one urinary incontinence episode for week in the last month
• pelvic floor muscle strength equal or greater than 2 assessed by Oxford Modified Rating Score