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Study identifier: NCT06094543 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Improving Overactive Bladder Treatment Access and Adherence

Condition: Overactive Bladder Syndrome · Urinary Incontinence  ·  Sponsor: Stanford University

PhaseNA
Planned participants30
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersYes

About this study

Overactive bladder (OAB) and urinary incontinence (UI) are chronic debilitating and embarrassing conditions that affect 33 million Americans. Yet, both are underdiagnosed and undertreated with significant financial and health-related consequences. OAB syndrome is characterized by urinary urgency, with and without urinary incontinence, urinary frequency, and nocturia. Evidence-based treatments are available, including behavioral therapy, pharmacotherapy, and minimally invasive procedures. Diagnosis and treatment are also associated with improvement in urinary symptoms and overall quality of life (QOL).3 However, 70-80% of treated patients will discontinue use of therapy in the first year due to one of several factors (e.g., cost, tolerability, inadequate effect). In addition, only 4.7% progress to advanced therapies suggesting undertreatment for those that need it most. Vulnerable populations are especially at risk, as therapy utilization are lowest among older, lower income, and/or minority groups. Poor access, insufficient patient education regarding disease chronicity, expected outcomes, costs, and potential side effects lead to unrealistic patient perceptions about therapy. This leads to suboptimal therapy duration, poor treatment efficacy, adherence, and undertreatment. The study aims to evaluate a tailored patient-centered tool to begin the treatment process.

This description comes directly from the study's public registry record.

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Locations (1)

Stanford Pelvic Health CenterRedwood City, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06094543