ACTIVE_NOT_RECRUITING

Improving Primary Care Access to Urinary Incontinence Treatment for Women Veterans

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 PURSUIT project aims to improve access to evidence-based nonsurgical UI treatment for women Veterans in the Southeast region of the United States using the most effective remote delivery modality. Using cluster randomization, the study will compare two models at the practice level: (1) the use of a practice facilitation toolkit with a mHealth UI modality alone and (2) the practice facilitation toolkit with a mHealth UI model combined with education on clinical pathways for consultation. Patient level outcomes related to UI symptom improvement will be compared. Patient and provider perceptions of factors that could influence future remote UI treatment scalability will also be assessed. All primary care practices will receive practice facilitation with a PURSUIT toolkit that includes (1) 1-2 visits with a practice facilitator; (2) mobile-health or mHealth application training (MAT); 3) online resource hub; and (4) health information technology (HIT) assistance. PURSUIT's future goal is to disseminate the most effective modality for delivering nonsurgical UI treatment for women Veterans nationally within the VHA.

Official Title

Improving Primary Care Understanding of Resources and Screening for Urinary Incontinence to Enhance Treatment

Quick Facts

Study Start:2022-11-01
Study Completion:2026-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05438849

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:20 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Veteran
  2. * English-speaking, community-dwelling women Veterans
  3. * Diagnosis of UI (all types)
  4. * Access to the internet via a mobile device or computer
  1. * Women Veterans who are currently pregnant or less than 12 weeks postpartum

Contacts and Locations

Principal Investigator

Alayne D Markland, DO, MSc
PRINCIPAL_INVESTIGATOR
UNIVERSITY OF ALABAMA AT BIRMINGHAM, BIRMINGHAM , AL

Study Locations (Sites)

Birmingham VA Healthcare System
Birmingham, Alabama, 35233
United States
Atlanta VA Health Care System
Decatur, Georgia, 30033
United States

Collaborators and Investigators

Sponsor: University of Alabama at Birmingham

  • Alayne D Markland, DO, MSc, PRINCIPAL_INVESTIGATOR, UNIVERSITY OF ALABAMA AT BIRMINGHAM, BIRMINGHAM , AL

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 Date2022-11-01
Study Completion Date2026-01

Study Record Updates

Study Start Date2022-11-01
Study Completion Date2026-01

Terms related to this study

Keywords Provided by Researchers

  • women
  • Veterans
  • behavioral treatment
  • primary care

Additional Relevant MeSH Terms

  • Urinary Incontinence