Simulation-Based Learning Experience in Strengthening Stoma Care Education
- Conditions
- Stoma
- Registration Number
- NCT06749769
- Lead Sponsor
- Nuran Ayşen Pamir Aksoy
- Brief Summary
The goal of this clinical trial is to investigate the effectiveness of simulation-based learning experience in enhancing stoma care education on patients with stoma.
The main hypothesis it aims to test are:
H1: Simulation-based learning experience is effective in reducing stoma patients' concerns about performing stoma care.
H2: Simulation-based learning experience is effective in increasing stoma patients' stoma care skills.
H3: Simulation-based learning experience is effective in increasing stoma patients' perceived self-efficacy regarding stoma care.
Researchers will compare the control and study group to see if the simulation-based learning enhances the patients learning experience.
Participants will be asked to;
* Answer the questions (demographic data form and anxiety scale)
* Receive education regarding stoma care (verbal and demonstration)
* Practice stoma care on their own
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 70
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Stoma Care Skills Rubric Post-operative 3rd day It consists of 23 items that include stoma care process steps. The learner's competence for each process step is scored between 0-2 (0- Insufficient 1- Partially sufficient 2- Sufficient). A minimum of 0 and a maximum of 46 points can be obtained. The total score shows the competence of stoma care skills.
Generalized Perceived Self-Efficacy Scale at the time of enrollement, and Post-operative 3rd day It consists of 10 items, and each item of the scale is scored between 1 and 4. These are listed as not true (1), somewhat true (2), more true (3), and completely true (4). Minimum of 10 and a maximum of 40 points can be obtained. The higher the score, the higher the individual's perceived self-efficacy.
- Secondary Outcome Measures
Name Time Method State Anxiety Level at the time of enrollement, and post-operative 3rd day In the study, the state anxiety scale will be used to determine the anxiety levels of the patients during the application. The State Anxiety Scale (SAS) provides information about what the individual feels at that moment. The State Anxiety Scale is a Likert-type scale consisting of 20 items, rated between 1 (not at all) and 4 (completely).
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
Trial Locations
- Locations (2)
Acibadem Altunizade Hospital
🇹🇷Istanbul, Other, Turkey
Acibadem Atakent Hospital
🇹🇷Istanbul, Other, Turkey