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Clinical Trial Summary

The goal is to investigate the feasibility and effects of adding "wearables for the bladder" devices to conventional pelvic floor physical therapy (PFPT) to bladder function, in people with multiple sclerosis (MS).


Clinical Trial Description

The participants baseline pelvic floor and bladder function will be assessed by a pelvic floor physical therapist as per standard care, and online MS-symptom questionnaires (i.e., quality of life, bladder bother/symptoms, falls, fatigue, depression). Participants will be trained on the maintenance and use of "wearable for the bladder" (WeB) devices. Participants will receive standard PFPT intervention care, and will be asked to further train using the WeB devices. 8-10 sessions will be conducted over telehealth or in person as per standard protocol. At 12 weeks, participants will return to clinic for pelvic floor and bladder function assessment. A control group will receive standard PFPT intervention care as well as online MS-symptom questionnaires. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05715268
Study type Interventional
Source University of California, San Francisco
Contact Valerie J Block, DPTSc
Phone ?+1 (415) 502-7208
Email valerie.block@ucsf.edu
Status Recruiting
Phase N/A
Start date March 15, 2023
Completion date September 2024

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