- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07689422
The Effect of Web-Based Gamification Applications on Nursing Students' Learning Regarding Cardiopulmonary Resuscitation
In this study, the aim was to determine students' level of knowledge regarding cardiopulmonary resuscitation by using web-based gamification applications in nursing education, and additionally, to evaluate the secondary effects on knowledge retention and skill levels.
- The cardiopulmonary resuscitation training delivered through web-based gamification applications has no effect on students' level of knowledge.
- The cardiopulmonary resuscitation training delivered through web-based gamification applications has an effect on students' level of knowledge.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Trabzon
-
Trabzon, Trabzon, Turkey (Türkiye), 61080
- Karadeniz Technical University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Must be registered for the Surgical Nursing course for the first time,
- Must have internet access,
- Must have a computer, tablet, or mobile phone,
- Must be willing to participate in the research.
Exclusion Criteria:
- Not attending the theoretical course,
- Not having received any previous training in cardiopulmonary resuscitation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control group
|
|
|
Experimental: web-based gamification application group
|
This application consists of various question contents of different types. When the student enters the application, he/she sees the practice questions and the countdown timer for the specified time on the screen. The student has the opportunity to track his/her total score and average ranking within the class after each exercise he/she solves on the leaderboard. In this practice, questions were prepared based on the procedural steps in the skill assessment forms, enabling students to reinforce their psychomotor skills. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Level of knowledge
Time Frame: At baseline and at 4 weeks
|
To assess students' level of knowledge regarding cardiopulmonary resuscitation before and after the educational intervention.
|
At baseline and at 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Skill level
Time Frame: At baseline and at 4 weeks
|
To assess students' skills in cardiopulmonary resuscitation after the educational intervention.
|
At baseline and at 4 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge retention
Time Frame: 4 weeks after baseline
|
Assessment of students' cardiopulmonary resuscitation knowledge retention at 4 weeks post-education.
|
4 weeks after baseline
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Tuğba Özcan Kaya, Karadeniz Technical University Faculty of Health Sciences Department of Nursing
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- TOzcan
- Scientific Research Project (Other Identifier: Karadeniz Technical University)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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