The Effect of the Training Program Given to Permanent Colostomy Patients on Self-efficacy
Recruiting · NCT06905925 · Interventional (participants receive a specific treatment) · Lead sponsor: Cukurova University
View the official record on ClinicalTrials.gov →Interventions studied
The group receiving counseling
What this trial is about
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.
Who can take part
Age range
18 Years to 100 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
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.
Where it is running
1 location listed.
- Adana City Training and Research Hospital - Adana, Yüreğir, Turkey (Türkiye)