- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05865509
Comparison of the Escape Room and Storytelling Methods in Learning the Stress Response
May 9, 2023 updated by: Nilgun Dogu, Ankara Medipol University
Comparison of the Escape Room and Storytelling Methods in Learning the Stress Response: A Randomized Controlled Study
The goal of this randomised controlled study is to evaluate the effects of storytelling and escape room methods on the level of learning about stress response of nursing students and students' opinions about these methods.
The main questions it aims to answer are:
- Is there a difference between the pretest-posttest scores of the students who received training on stress response with the escape room method?
- Is there a difference between the pretest-posttest scores of the students who were trained on the stress response with the storytelling method?
- Is the difference between the knowledge levels of the students who received stress response training with the escape room and storytelling methods statistically significant? The students, who received training on stressors, stress response and the long-term effects of stress through lecture, were divided into two groups four weeks after this training and were retrained on the same subject with escape room and storytelling methods. Before and after the Escape room and storytelling practices, the students' knowledge of the stress response was evaluated. After both applications, focus group discussions were held with the students and their opinions and feedbacks on the applications were evaluated.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
35
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Ankara, Turkey
- Nilgün Doğu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
Nursing students taking internal medicine course
Exclusion Criteria:
N/A
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Escape room
This group received training on stress response using the escape room method.
|
Students were given training on stress response using the escape room method.
|
|
Experimental: Storytelling
This group received training on stress response using the storytelling method.
|
Students were given training on stress response using the storytelling method.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge levels of students about stress response before the application.
Time Frame: On intervention day, just before application
|
The knowledge level of the students about the stress response was evaluated by means of a form developed by the researchers after reviewing the literature.
Students' Knowledge Assessing Form about the Stress Response, consisting of ten questions.
The questions in the Students' Knowledge Assessing Form about the Stress Response were evaluated by a total of nine experts according to the Davis technique in terms of comprehensibility and content validity, and the content validity was found to be 1 (>0.80).
Results from the Students' Knowledge Assessing Form about the Stress Response were evaluated based on the number of correct answers.
|
On intervention day, just before application
|
|
Knowledge levels of students about stress response after the application
Time Frame: On intervention day, immediately after application
|
After the application, the knowledge levels of the students about stress response re-evaluated with the "Students' Knowledge Assessing Form about the Stress Response".
After the application, the knowledge levels of the students about stress response re-evaluated with the "Students' Knowledge Assessing Form about the Stress Response".
The difference between the knowledge levels of the students in the Escape room and Storytelling groups before and after the application was statistically evaluated using Mann Whitney U and Wilcoxon tests.
|
On intervention day, immediately after application
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 13, 2022
Primary Completion (Actual)
December 13, 2022
Study Completion (Actual)
December 13, 2022
Study Registration Dates
First Submitted
April 6, 2023
First Submitted That Met QC Criteria
May 9, 2023
First Posted (Actual)
May 19, 2023
Study Record Updates
Last Update Posted (Actual)
May 19, 2023
Last Update Submitted That Met QC Criteria
May 9, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 20221312
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.