Improving Overactive Bladder Treatment Access and Adherence

This study is looking at a new way to help people with overactive bladder (OAB) and urinary incontinence (UI) better manage their condition. It's testing an 8-week daily "Patient Engagement Tool" which is a behavioral intervention designed to educate and involve patients in their treatment. You might be able to join if you are a woman aged 18 or older, have had OAB symptoms for at least 3 months, and can speak English or Spanish. You can participate if you haven't had behavioral treatment before, or if you've been treated for OAB in the past but haven't had supervised pelvic floor physical therapy or medication within the last year. The researchers want to see how easy the tool is to use and how much it improves your knowledge about bladder health after 12 weeks. The current status of this study is unclear, and it plans to enroll 30 participants.

Study design
This is an interventional study, meaning participants will receive a specific intervention. It plans to enroll 30 women.
What's involved
You would use a daily patient engagement tool for 8 weeks. Your usability of the tool and bladder health knowledge will be measured at 12 weeks.
Compensation
Not stated in the trial record.
Follow-up
Your progress will be assessed at 12 weeks after starting the intervention.

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NCT06094543

Improving Overactive Bladder Treatment Access and Adherence

Recruiting
NAAges 18+InterventionalTreatment
Stanford University
~30 participants
Updated 2026-07-21 on ClinicalTrials.gov
What's tested:Patient Engagement Tool

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Systems Usability Scale (SUS)
Measured over 12 weeks
+1 more outcome measured
Overactive Bladder Syndrome
Urinary Incontinence
1 sites across 1 states
California1

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Eligibility criteria

Inclusion

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

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)
  • Systems Usability Scale (SUS)12 weeks

    Usability, engagement, Patient engagement tool reliability/accessibility (technical issues)

  • Bladder Health Knowledge, Attitudes, and Beliefs (KAB)12 weeks

    Will assess knowledge about bladder health 1. Knowledge: Awareness and understanding of normal bladder function, signs and symptoms of dysfunction (e.g., incontinence, urgency), and available treatment or prevention strategies. 2. Attitudes: Perceptions and feelings toward bladder health, such as embarrassment, stigma, or normalization of symptoms like leakage or urgency. 3. Beliefs: Individual or cultural beliefs about the causes, severity, and treatability of bladder problems, which may influence care-seeking behavior.