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Implementing a Mobile Health Application for Women Veterans With Urinary Incontinence (MyHealtheBladder): Function QUERI 3.0
Implementing a Mobile Health Application for Women Veterans With Urinary Incontinence: MyHealtheBladder in Function QUERI 3.0 (QUE 25-008)
Who can join
All ages · Women
Full eligibility criteria
Inclusion Criteria: Site Inclusion Criteria: * Facility is part of the U.S. Department of Veterans Affairs (VA) health system. * Clinic serves at least 100 Women Veterans annually. * Identified site champion (e.g., clinician or staff member) who is willing to assume required program responsibilities for implementation. Patient Inclusion Criteria: * Women Veterans * Have any type of Urinary Incontinence existing for at least 3 months Exclusion Criteria: Site Exclusion Criteria: * Clinic has already implemented the MyHealtheBladder program. Patient Exclusion Criteria: * No access to computer or mobile device * No email account * Institutionalized
About the study
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.
What is being tested
- Implementation Strategy: Foundational Arm (other)
- Implementation Strategy: REACH Arm (other)
Sponsor: VA Office of Research and Development · Participants: 20 · Started: Apr 30, 2026
Contact the study team
- Caitlin B Kappler, MSW · Phone: (919) 286-6936
Official record on ClinicalTrials.gov — NCT07219433
Locations in the U.S.
| North Carolina | Durham VA Medical Center, Durham, NC, Durham |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.