NCT05715268Active, not recruiting
Wearables for the Bladder: an In-home Treatment Feasibility Pilot Study
Moving MS Bladder Dysfunction Into the 21st Century: Developing Novel and Accessible Ways to Treat Dysfunction in the Home - a Three Month Single Arm Open Label Feasibility Pilot With Waitlist Control
Source: ClinicalTrials.gov · Last updated 8 Jul 2026
Brief summary (registry, in English)
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).
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- First submitted
- 26 Jan 2023
- Start date
- 15 Mar 2023
- Primary completion date
- 21 Dec 2026
- Lead sponsor
- University of California, San Francisco
- Diseases
- Multiple sclerosis
- NCT number
- NCT05715268
What you commit to
- Study type: Interventional
- Planned participants: 20
- From 15 Mar 2023 to the primary completion date, 21 Dec 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Current urinary tract infection
- Any cognitive, dexterity or visual impairment so severe that it precludes use of the wearables for the bladder tool or ability to use a smartphone
Other
- Undergone treatment for bladder dysfunction symptoms within 3 months
- Recent (\~30 days) relapse
- Pregnancy
Who the study is looking for
- MS diagnosis
- Assigned Female at birth and whose sex is currently Female
- Mild/moderate bladder dysfunction (bowel/bladder functional systems scores = 0-2 or Bladder control scale \>0)
- California residents
- Wifi in the home and personal smartphone (using Apple operating system)
- Able to walk with or without assistive device
- Manual muscle test score of 2 or more.
Age in the registry: 18 years to 80 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of California San Francisco, Weill Institute for Neurosciences Coordinator of this site? Confirm its status | San Francisco | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.