Ostomy Simulation for Patient Education Prior to Urologic Bowel Diversion Surgeries

Recruiting N/A Interventional Study
Ostomy Ileal Conduit
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Device Feasibility
Participants needed
40 (estimated)
Sponsor
University of Minnesota · Other
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About This Trial
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) a…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age\>18, undergoing bowel diversion urologic surgery. Exclusion Criteria: * Current or prior ostomy formation, cognitive function causing inability to care for stoma, current pregnancy.
Contacts

Bowan Yao, MD

612-625-7486

yao00235@umn.edu

CONTACT