A Practice-Based Intervention To Improve Care for a Diverse Population Of Women With Urinary Incontinence (NCT05534412)
🩺 Plain-English Summary (8th-Grade Level)
The main goal of this clinical trial is to improve the care for urinary incontinence (UI) provided to adult women by primary care providers. The main questions it aims to answer are: * Can a practice-based intervention involving primary care providers lead to improved quality of incontinence care? * Will this intervention reduce the utilization of specialist care for urinary incontinence? * What effect will this intervention have on patient outcomes, including disease-specific outcomes, symptom severity, quality of life, and patient knowledge? * Does our intervention reduce disparities in care? Provider participants will be randomized at the office level to either an intervention group or a delayed intervention (control) group. The intervention group will receive an intervention consisting of academic detailing, clinical decision support tools, electronic referral, and the ability to refer to an advanced practice provider for co-management. The delayed intervention group will provide usual care until the crossover phase of the study, at which point they will receive the same intervention as the intervention group. Patient participants will bring up urinary incontinence with their primary care provider and complete three electronic surveys. Researchers will compare the intervention group to the delayed intervention (control) group to see if the intervention results in increased adherence to evidence-based quality indicators.
Who can join: Review the eligibility criteria below.
Location: University of California, San Diego — La Jolla, California
Age range: 18 Years
🧪 Interventions in This Study
- Academic Detailing (OTHER)
- Electronic Clinical Decision Support (OTHER)
- APP Co-management (OTHER)
- Electronic Referral (OTHER)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (4 Sites)
- University of California, San Diego — La Jolla, California
- Cedars-Sinai — Los Angeles, California
- University of California, Los Angeles — Los Angeles, California
- Harbor-UCLA Medical Center — Torrance, California
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Urinary Incontinence
- Improving Primary Care Access to Urinary Incontinence Treatment for Women Veterans — Birmingham, Alabama
- Group Versus Individual Physiotherapy for Urinary Incontinence in Aging Women — Montreal, Quebec
- Clinical Study of External Electrical Stimulation for Male Incontinence — Monroe, Connecticut
- Use of Sildenafil for Treatment of Urinary Incontinence — Galveston, Texas
- WI-INTUIT: Bridging Community Based Continence Promotion and Primary Care — San Diego, California
Explore by condition: All Urinary Incontinence clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.