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.
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