NCT lookup
Pull any trial record directly from ClinicalTrials.gov.
Wearables for the Bladder: an In-home Treatment Feasibility Pilot Study
Wearables for the Bladder: an In-home Treatment Feasibility Pilot Study
Active Not RecruitingNA
Sponsor: University of California, San Francisco
Conditions: Multiple Sclerosis, Urinary Bladder, Overactive
Interventions: WeB, Standard pelvic floor physical therapy
Countries: United States
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).
Eligibility overview
Sex: FEMALE
Age: 18 Years to 80 Years
Healthy volunteers: No
Study type: INTERVENTIONAL
Eligibility criteria
Inclusion Criteria: * 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. Exclusion Criteria: * Undergone treatment for bladder dysfunction symptoms within 3 months * Current urinary tract infection * Recent (\~30 days) relapse * 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 * Pregnancy
Locations (1)
- San Francisco, California, United States