RECRUITING

A Practice-Based Intervention To Improve Care for a Diverse Population Of Women With Urinary Incontinence

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

A Practice-Based Intervention To Improve Care for a Diverse Population Of Women With Urinary Incontinence

Quick Facts

Study Start:2022-09-07
Study Completion:2025-02
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05534412

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Jennifer Anger, MD
CONTACT
3108479299
janger@health.ucsd.edu
Kyle Okamuro, BS
CONTACT
3104631464
kyokamuro@health.ucsd.edu

Study Locations (Sites)

University of California, San Diego
La Jolla, California, 92037
United States
Cedars-Sinai
Los Angeles, California, 90048
United States
University of California, Los Angeles
Los Angeles, California, 90095
United States
Harbor-UCLA Medical Center
Torrance, California, 90502
United States

Collaborators and Investigators

Sponsor: University of California, San Diego

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-09-07
Study Completion Date2025-02

Study Record Updates

Study Start Date2022-09-07
Study Completion Date2025-02

Terms related to this study

Keywords Provided by Researchers

  • Practice-based intervention
  • Patient-centered outcomes research
  • Disparities
  • Quality of care indicators
  • Primary care
  • Urinary incontinence
  • Stress incontinence
  • Urge incontinence
  • Mixed incontinence
  • Overactive bladder

Additional Relevant MeSH Terms

  • Urinary Incontinence