RECRUITING

Ostomy Simulation for Patient Education Prior to Urologic Bowel Diversion Surgeries

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 purpose of this study is to evaluate the feasibility of using a realistic and anatomically accurate 3D printed simulation model for urologic bowel diversion patient education. Using a randomized two group design, we aim to determine whether the use of this model enhances patient knowledge, self-care skills, and confidence in ostomy care. We will also evaluate changes in quality of life (QOL) and patient satisfaction comparing patients exposed to the 3D model to those receiving standard of care. The secondary aim of the study is to examine the differences between groups on patient outcomes including hospital duration, mortality, emergency/urgent health care visits, readmissions, and infections. Participants will be educated using 3D model simulation as part of their preoperative education (experimental group) or have standard education without using the simulation model (comparator group). Both groups will complete quality of life (QOL), ostomy adjustment, and satisfaction with education surveys during their preoperative education visit and again during their routine follow-up visits (a) within 3 weeks after surgery, (b) between 5- 8 weeks after surgery, and (c) at approximately 3 months after surgery.

Official Title

3D Ostomy Simulation for Patient Education

Quick Facts

Study Start:2024-07-30
Study Completion:2026-07-15
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06583577

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:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age\>18, undergoing bowel diversion urologic surgery.
  1. * Current or prior ostomy formation, cognitive function causing inability to care for stoma, current pregnancy.

Contacts and Locations

Study Contact

Bowan Yao, MD
CONTACT
612-625-7486
yao00235@umn.edu

Study Locations (Sites)

University of Minnesota
Minneapolis, Minnesota, 55454
United States

Collaborators and Investigators

Sponsor: University of Minnesota

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 Date2024-07-30
Study Completion Date2026-07-15

Study Record Updates

Study Start Date2024-07-30
Study Completion Date2026-07-15

Terms related to this study

Keywords Provided by Researchers

  • Patient education
  • Simulation
  • Quality of life
  • Ostomy adjustment

Additional Relevant MeSH Terms

  • Ostomy
  • Ileal Conduit