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Improving Overactive Bladder Treatment Access and Adherence

Stanford University · with National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) · NCT06094543

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18+ · Women only
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
30
US sites recruiting
1
Study start
November 1, 2024
Record last updated
July 21, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: Patient Engagement Tool

Conditions: Overactive Bladder Syndrome; Urinary Incontinence

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Female aged 18 years or older
  • OAB symptoms for at least 3 months
  • English/Spanish language skills and cognitive status sufficient to complete all study related materials
  • Behavioral treatment naïve patients
  • Previously treated OAB patients without supervised pelvic floor physical therapy or pharmacotherapy within 1 year

Exclusion Criteria

  • Post void residual urine > 150ml
  • Confirmed diagnosis of Interstitial Cystitis/Painful Bladder Syndrome (IC/PBS)
  • Pregnant or breastfeeding patients
  • Patients residing in a nursing home
  • Comorbid neurological conditions, including spinal cord injury, progressive neurologic illnesses (e.g. Multiple Sclerosis, Parkinson's disease) or central nervous system disease (e.g. brain tumor, stroke)
  • Stage 2 or greater pelvic organ prolapse
  • Any history of urethral stricture
  • Any history of pelvic irradiation
  • Any history of bladder malignancy
  • Current symptomatic urinary tract infection (UTI), unresolved by the time of enrollment
  • Hematuria without a clinical evaluation
  • History or current use of indwelling urinary foley catheterization, suprapubic tube or intermittent catheterization
  • Patients with UI treated with onabotulinumtoxinA, sacral neuromodulation, or percutaneous tibial nerve stimulation (third line therapies)

Recruiting US locations

  • Stanford Pelvic Health Center

    Redwood City, CA 94062

    Site contact: Ekene Enemchukwu, MD, MPH · 650-723-1867 · oab.matters@stanford.edu

Improving Overactive Bladder Treatment Access and Adherence (NCT06094543) | Bored Studies