- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07276659
The Contribution of Scenario Writing to Learning Stoma Care in Nursing Education: A Mixed-Methods Quasi-Experimental Intervention Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This mixed-methods quasi-experimental study investigates the impact of scenario-based learning on nursing students' acquisition of stoma care knowledge. Third-year nursing students who previously completed the surgical nursing course were eligible for participation. The intervention group engaged in an eight-week Scenario-Based Stoma Care Learning Program, which included (1) preparation and writing of clinical scenarios, (2) dramatization and role-play activities using simulated clinical environments, and (3) structured instructor-guided feedback. The control group did not receive any additional training and completed only the pre-test and post-test assessments.
The pre-test measuring stoma care knowledge was administered on October 27, 2025. The post-test was administered on December 22, 2025, following completion of all scenario-based learning sessions. After the educational intervention, qualitative data were collected from the intervention group through focus group interviews using a COREQ-aligned semi-structured interview guide. Qualitative data aim to explore changes in participants' confidence, perceived skills, learning processes, and their experience with scenario writing and role-play.
The study's primary objective is to determine whether scenario-based learning improves students' stoma care knowledge. Secondary objectives include understanding how scenario writing and dramatization influence students' confidence, engagement, and perceived competence in performing stoma care.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Van, Turkey (Türkiye), 65090
- Van Yuzuncu Yil Univeristy
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being a 3rd-year undergraduate nursing student in the Nursing Department.
- Having successfully completed the Surgical Nursing course in the 2nd year.
- Voluntarily agreeing to participate in the study and providing informed consent.
Exclusion Criteria:
- Students who did not pass the Surgical Nursing course.
- Students who have previously received professional stoma care training.
- Students who complete the data collection forms incompletely.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Scenario-Based Stoma Care Education
Participants in the intervention arm will receive an 8-week scenario-based stoma care education program. The intervention includes:
|
A structured scenario-writing and role-play-based educational program delivered over 8 weeks.
Students develop stoma care scenarios, present them, and perform role-play using simulated patients and a skills laboratory environment.
The intervention includes scenario writing sessions (4 weeks) and stoma care role-play practice using manikins and real materials (4 weeks), followed by structured educator feedback.
|
|
No Intervention: Control Group
Participants in the control arm will not receive any additional education or training. They will complete the same pre-test and post-test assessments as the intervention group. No scenario writing or role-play activities will be administered. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stoma Care Knowledge Score
Time Frame: Baseline (Week 0) and Post-intervention (Week 8)
|
Change in students' stoma care knowledge score from pre-test to post-test.
Knowledge will be measured using a 20-item Stoma Care Knowledge Questionnaire developed by the research team.
Scores range from 0 to 20, with higher scores indicating greater knowledge.
The primary analysis will compare post-test scores between the intervention and control groups, adjusting for baseline knowledge.
|
Baseline (Week 0) and Post-intervention (Week 8)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Qualitative Themes Related to Students' Perceived Confidence and Skill Development
Time Frame: Immediately after completion of the 8-week intervention (same week as the post-test).
|
Semi-structured focus group interviews will be conducted with participants in the intervention group after completion of the 8-week program.
Qualitative analysis (thematic analysis) will explore changes in perceived confidence, perceived competence, motivation for practice, and learning experiences related to scenario writing and role-play activities.
Themes will be identified using coded transcripts analyzed with MAXQDA by two independent researchers.
|
Immediately after completion of the 8-week intervention (same week as the post-test).
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: hatice akaltun, PhD, Yuzuncu Yil University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- VYYU-SBF-HAKALTUN-002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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