Actively Recruiting
Implementing a Mobile Health Application for Women Veterans With Urinary Incontinence (MyHealtheBladder): Function QUERI 3.0
Led by VA Office of Research and Development · Updated on 2026-05-07
20
Participants Needed
1
Research Sites
230 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Implementing a Mobile Health Application for Women Veterans with Urinary Incontinence (MyHealtheBladder): Function QUERI 3.0 aims to compare implementation approaches while also gathering information on clinical effects of the Evidence-Based Program (EBP) in its new context and focusing on equitable reach (extent to which the program serves all members of its intended audience). The overall goal is to implement, evaluate, and sustain MyHealtheBladder in 20 VA facilities using a type III effectiveness-implementation hybrid study framework and parallel cluster randomized trial (CRT) design.
CONDITIONS
Official Title
Implementing a Mobile Health Application for Women Veterans With Urinary Incontinence (MyHealtheBladder): Function QUERI 3.0
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Facility is part of the U.S. Department of Veterans Affairs (VA) health system.
- Clinic serves at least 100 Women Veterans annually.
- Clinic is located at least 25 miles from the nearest other VA clinic participating in the program.
- Identified site champion willing to take on program responsibilities for implementation.
- Women Veterans.
- Have any type of urinary incontinence lasting at least 3 months.
You will not qualify if you...
- Clinic has already implemented the MyHealtheBladder program.
- No access to a computer or mobile device.
- No email account.
- Institutionalized (living in a hospital, nursing home, or similar facility).
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Durham VA Medical Center, Durham, NC
Durham, North Carolina, United States, 27705-3875
Actively Recruiting
Research Team
C
Caitlin B Kappler, MSW
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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