- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06755879
the Impact of a Digital Game-based Learning Activity on Nursing Students' Understanding of Surgical Site Infections
the Impact of a Digital Game-based Learning Activity on Nursing Students' Learning and Motivation Levels Regarding Surgical Site Infection Prevention Initiatives
The aim of this randomized controlled trial was to evaluate the effect of a digital game-based learning activity on students' learning of interventions to prevent surgical site infections.This study will seek answers to the following questions:
Is digital game-based learning activity effective in students' learning process? Is the traditional method of theoretical lecturing effective in the learning process? What is the effect of students' learning methods on their motivation? The researchers will compare the group with the theoretical lecture to see the effectiveness of the digital game-based learning activity.
Participants will be divided into 3 groups. In the first group, the level of learning interventions to prevent surgical site infections with digital game-based learning activity will be evaluated with pre-test and post-test In the second group, the level of learning the theoretical course and interventions to prevent surgical site infections will be evaluated with pre-test and post-test.
The control group will be evaluated only with the pre-test post-test without any intervention.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
VAN, Turkey, 65000
- Van Yüzüncü Yıl Üniversitesi /Sağlık Bilimleri Fakültesi
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Having a cell phone, computer or tablet device.
- To have internet access on one of the cell phone, computer or tablet devices.
- To have taken the Surgical Diseases Nursing course.
- To be a 4th year student of Van Yüzüncü Yıl University Faculty of Health Sciences, Department of Nursing
- Volunteering to participate in the research
Exclusion Criteria:
- - Graduating from a health vocational high school or coming from a health-related department with vertical transfer
- Limited ability to read and write in Turkish.
- Not having a software infrastructure suitable for opening digital game activities on mobile phones, computers or tablet devices
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: digital game-based learning activity group
the level of learning interventions to prevent surgical site infections with digital game-based learning activity will be evaluated with pre-test and post-test
|
learning interventions to prevent surgical site infections with a digital game-based learning activity
|
|
Active Comparator: theoretical course group
the level of learning the theoretical course and interventions to prevent surgical site infections will be evaluated with pre-test and post-test
|
Evaluation of the effectiveness of students' learning of interventions to prevent surgical site infections in the theoretical course taught by traditional method
|
|
No Intervention: control group
The control group will be evaluated only with the pre-test post-test without any intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
pre-test post-test question form
Time Frame: after the pre-test is applied, the digital game-based learning activity will be used for 5 days. the post-test will be applied 3 weeks after the pre-test
|
the effectiveness of the digital game-based learning activity will be measured by pre-test post-test (Measurement will be made with a pre-test post-test prepared by the researcher.)
|
after the pre-test is applied, the digital game-based learning activity will be used for 5 days. the post-test will be applied 3 weeks after the pre-test
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
pre-test post-test question form
Time Frame: After the pre-test is applied, a 45-minute theoretical lesson will be held with the students. Post-test will be applied 3 weeks after the pre-test
|
pre-test post-test will be applied to evaluate the effectiveness of theoretical explanation with traditional method (Measurement will be made with a pre-test post-test prepared by the researcher.)
|
After the pre-test is applied, a 45-minute theoretical lesson will be held with the students. Post-test will be applied 3 weeks after the pre-test
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
the effect of teaching methods on student motivation
Time Frame: measurement will be made with 3 weeks between pre-test and post-test
|
'Teaching material motivation scale' will be applied at the end of the study to determine the effect of teaching methods on student motivation This scale is used to determine the motivation towards a material based on a single application where the user is only dependent on the material.
A high score on the total or average score of the scale indicates that the individual's motivation towards the material being evaluated is positively high.
|
measurement will be made with 3 weeks between pre-test and post-test
|
Collaborators and Investigators
Sponsor
Collaborators
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
- VYYU-SBF-HAKALTUN-001
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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