Using a 3D model to educate patients before urologic bowel surgeries
3D Ostomy Simulation for Patient Education
This study is testing if using a 3D model to teach patients about urologic bowel surgeries can help them understand their care better and improve their overall experience.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Minnesota Academic / other |
| Locations | 1 site (Minneapolis, Minnesota) |
| Trial ID | NCT06583577 on ClinicalTrials.gov |
What this trial studies
This study evaluates the feasibility of a realistic 3D printed simulation model for educating patients undergoing urologic bowel diversion surgeries. Participants will be randomly assigned to either receive standard education or education supplemented with the 3D model. The study aims to assess improvements in patient knowledge, self-care skills, confidence in ostomy care, and overall quality of life. Additionally, it will track patient outcomes such as hospital duration, readmissions, and satisfaction with care.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 who are planning to undergo bowel diversion urologic surgery.
Not a fit: Patients with current or prior ostomy formation or cognitive impairments that hinder their ability to care for a stoma may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance patient preparedness and confidence in managing their ostomy, leading to better quality of life post-surgery.
How similar studies have performed: While the use of simulation in medical education is gaining traction, this specific application in ostomy education is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion 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.
Where this trial is running
Minneapolis, Minnesota
- University of Minnesota — Minneapolis, Minnesota, United States (Recruiting)
Study contacts
- Study coordinator: Bowan Yao, MD
- Email: yao00235@umn.edu
- Phone: 612-625-7486
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.