COMPLETED

EHR-integrated rUTI Texting Platform

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 goal of this clinical trial is to compare a texting platform to usual care for managing recurrent urinary tract infections (UTI). The main question it aims to answer is: • can a texting platform that integrates symptom triage and prevention education reduce the rate of unnecessary antibiotics for recurrent UTIs as compared to usual care? Participants enrolled onto the texting platform will: • receive evidence-based clinical guidance for the management of symptoms of UTI and receive educational videos on how to prevent UTIs. An important secondary outcome is to determine if the texting platform improves self-efficacy for the management of recurrent UTI.

Official Title

An EHR-integrated Texting Platform to Promote Self-management in Women With Recurrent Urinary Tract Infections

Quick Facts

Study Start:2024-03-07
Study Completion:2025-05-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06035601

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 to 100 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Provision of signed and dated informed consent form
  2. 2. Stated willingness to comply with all study procedures and availability for the duration of the study
  3. 3. Females who currently meet the criteria for recurrent UTIs
  4. 4. Age 18 years or older
  5. 5. Owns a mobile device with text messaging capability
  6. 6. Ability to read and write English
  7. 7. Currently receiving care from a provider in Penn Urogynecology or Penn Urology
  1. 1. History of known multidrug resistant UTIs
  2. 2. History of interstitial cystitis/bladder pain syndrome or current diagnosis of chronic pelvic pain
  3. 3. On continuous suppressive antibiotics currently
  4. 4. Currently pregnant or within 6 weeks of pregnancy
  5. 5. Transplant patient on immunosuppressive medication currently
  6. 6. Practice of chronic self-catheterization

Contacts and Locations

Study Locations (Sites)

University of Pennsylvania
Philadelphia, Pennsylvania, 19104
United States

Collaborators and Investigators

Sponsor: University of Pennsylvania

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 Date2024-03-07
Study Completion Date2025-05-31

Study Record Updates

Study Start Date2024-03-07
Study Completion Date2025-05-31

Terms related to this study

Keywords Provided by Researchers

  • unnecessary antibiotics
  • self-management
  • digital platform
  • texting
  • implementation science
  • recurrent UTI
  • healthcare utilization
  • patient education

Additional Relevant MeSH Terms

  • Recurrent Urinary Tract Infection