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Clinical Trials in Turkey / NCT06905925
Recruiting Not applicable

The Effect of the Training Program Given to Permanent Colostomy Patients on Self-efficacy

NCT06905925 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-06-23
Last updated
2025-09-12

Condition(s) studied

Stoma ColostomyColo-rectal Cancer

Investigational drug(s) / intervention(s)

The group receiving counseling

The group receiving counseling: Patients in the experimental group will receive pre-operative stoma care education from the researcher. This training is expected to last approximately 15 minutes. After the training, a brochure will be provided to the patients, which they can use if they need additional information. During the training process, patients will be informed that the researcher will contact them by phone during the 1st, 2nd, 3rd, and 4th weeks after discharge. During these calls, patients will be asked weekly (during weeks 1, 2, 3, and 4) about the color, odor, texture of the wound area, the function of the colostomy, and any complications. Additionally, at the end of the 2nd week, if there are no issues around the wound or sutures, patients will be called to the hospital for suture removal and dressing changes. In other weeks, dietary habits and the condition of the wound will also be inquired. During this four-week period, patients or their relatives will be informed that they can contact the researcher

Study summary

The planned research aims to evaluate the impact of a training program on self-efficacy in patients with permanent colostomies. It highlights the importance of holistic patient education in preventing complications and improving adaptation to stomas, which can positively affect patients' quality of life and self-efficacy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria: * • Patients scheduled for permanent colostomy following colorectal surgery, * Aged 18 years and older, * Conscious, with orientation to person, time, and place, * Able to speak Turkish, * Without auditory or visual impairments, * Using a phone, were included in the study. Exclusion Criteria:• Patients who could not be contacted during the study period, or those who developed post-operative complications (such as stenosis, necrosis, ileus, dermatitis, parastomal herniation, etc.) were excluded from the sample.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Adana City Training and Research Hospital Adana Yüreğir Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06905925 on ClinicalTrials.gov ↗ ← All trials in Turkey