Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06094543 · ClinicalTrials.gov registry record · NA

Improving Overactive Bladder Treatment Access and Adherence

A NA study of Urinary Incontinence and Overactive Bladder Syndrome, sponsored by Stanford University.

Recruiting
Registry status
NA
Development phase
30
Enrollment target
1
Study location

NCT06094543: Recruiting NA study of Urinary Incontinence and Overactive Bladder Syndrome, sponsored by Stanford University.

NCT06094543 is a NA study of Urinary Incontinence and Overactive Bladder Syndrome that is actively recruiting participants, run by Stanford University. The registered enrollment target is 30 participants, below the 261-participant average among 48 other Urinary Incontinence trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06094543, a NA study of Urinary Incontinence and Overactive Bladder Syndrome, is actively recruiting participants, sponsored by Stanford University.

RECRUITING
Registry status
NA
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

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.

Primary Outcome

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

Interventions

  • BEHAVIORAL Patient Engagement Tool

Study Locations (1)

California

  • Stanford Pelvic Health Center - Redwood City

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2024-11-01
Est. Completion 2026-12
Phase NA
Stanford University

1,744 total trials

What NCT06094543 shows while recruiting

NCT06094543 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 261-participant average among 48 other Urinary Incontinence trials with a reported enrollment target (89% lower).

The record links to 2 conditions, with Urinary Incontinence appearing as the primary indexed condition, and to 1 intervention - of which Patient Engagement Tool is the first listed.

NCT06094543 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT06094543 about?

NCT06094543 is a clinical study titled "Improving Overactive Bladder Treatment Access and Adherence". 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, wi...

What is the current status of trial NCT06094543?

This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2024-11-01. Estimated completion is 2026-12.

What conditions does trial NCT06094543 study?

This clinical trial studies the following conditions: Urinary Incontinence, Overactive Bladder Syndrome.

What interventions are being tested in trial NCT06094543?

The interventions under investigation include: Patient Engagement Tool (BEHAVIORAL).

Who is sponsoring clinical trial NCT06094543?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06094543 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Urinary Incontinence

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06094543's enrollment target sits among peer trials

30 37th of 48 higher than 11 of 48 other Urinary Incontinence trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Urinary Incontinence trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00977977 · 30 participants · Phase 2

    Rituximab Plus Cyclosporine in Idiopathic Membranous Nephropathy

  • NCT01459107 · 30 participants · Phase 2

    Human Upper Extremity Allotransplantation

  • NCT01666080 · 30 participants · NA

    Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)

  • NCT01720836 · 30 participants · Phase 1

    Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06094543, the US trial registry maintained by the National Library of Medicine. NCT06094543 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.