Stoma education and its effects on patients
Official title: Determining the Effects of Stoma Education on Patients' Self-Efficacy, Body Image, and Stoma Adherence
Run by Munzur University · NCT07464548 · Data updated 2026-11-12
This tests whether a teach-back stoma education program helps adults with a new colostomy or ileostomy feel more confident and manage their stoma better.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 90 Years |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Munzur University Academic / other |
| Drugs / interventions | radiation |
| Locations | 2 sites (Tunceli, City Center and 1 other locations) |
| Status | Recruiting |
| Started | March 10, 2026 |
| Main results expected | November 10, 2026 |
| Study ends | November 10, 2026 |
| Registry record updated | August 13, 2026 |
| Trial ID | NCT07464548 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults who have had elective colostomy or ileostomy surgery, have no diagnosed psychological disorders, and are willing and able to attend follow-up visits are ideal candidates.
✕Probably not a fit
Patients who had emergency surgery, have cognitive impairment or psychiatric disorders that prevent participation, or cannot comply with follow-up are unlikely to benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional program delivers a structured teach-back education session to adults after elective colostomy or ileostomy at Fırat University Hospital. Education covers stoma care techniques, appliance selection and fitting, complication recognition, and coping with body image changes, with teaching repeated until understanding is confirmed. Outcomes are measured by self-efficacy, body image scores, stoma-related complications, and adherence at baseline and during follow-up visits. Emergency surgery patients and those with cognitive or psychiatric conditions that prevent participation are excluded and participants must be able to attend follow-up visits.
Why it matters
Potential benefit: If successful, the program could improve patients' stoma self-care, reduce preventable complications, and boost confidence and body image.
How similar studies have gone: Teach-back approaches have improved knowledge and self-management in other surgical and chronic conditions, and limited stoma-specific data are promising but not extensive.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults who have undergone colostomy or ileostomy surgery. * Willingness to participate voluntarily in the study. * Elective surgery patients. * No diagnosed psychological disorders. Exclusion Criteria: * Emergency surgery cases. * Patients with cognitive impairment or psychiatric disorders preventing participation. * Patients unwilling to participate or unable to comply with study follow-ups.
Where it's running
-
Fırat University Hospital
Tunceli, City Center, Turkey (Türkiye) Recruiting -
Fırat University Hospital
Elâzığ, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Nilgün Söylemez, PhD
- Email: nilgunsoylemez@munzur.edu.tr
- Phone: +905439790424
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.