- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07794345
Planned Behaviour and Traditional Training
August 27, 2026 updated by: Mümin SAVAŞ
The Effect of Video Training of Virtual Reality Based on Theory of Planned Behaviour and Traditional Training on Students' Hand Hygiene Behaviours
The aim of this quasi-experimental study is to evaluate and compare the effectiveness of virtual reality (VR) headset-based hand hygiene education and classical theory-based education on the hand hygiene behaviors of primary school students.
The study was conducted with 195 primary school students divided into three groups: a VR education group, a classical education group, and a control group.
Data were collected using a socio-demographic form and the Hygiene Behavior Scale before and after the intervention to determine the change in students' hygiene habits.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This quasi-experimental study evaluated the effect of virtual reality (VR) headset-based education compared with classical planned behavior-based education on the hand hygiene behaviors of primary school students.
The study was conducted with 195 primary school students across three schools, categorized into an intervention group (VR training), a classical education group (theory-based training), and a control group (general information).
Data were collected using a socio-demographic form and the Hygiene Behavior Scale before and immediately after the intervention to assess group differences and changes in hygiene practices.
Study Type
Interventional
Enrollment (Actual)
195
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
-
-
Adıyaman Province
-
Adıyaman, Adıyaman Province, Turkey (Türkiye), 02040
- Adıyaman University
-
-
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
No
Description
Inclusion Criteria:
• Having a low hand hygiene level (39 points and above),
- Agreeing to participate in the study.
Exclusion Criteria:
• Wearing goggles,
- Suffering from any disease during the research,
- Withdrawing from the study.
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: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group 1 (VR Education)
Students received hand hygiene education using a virtual reality headset.
|
Interactive hand hygiene training delivered through virtual reality headsets
|
|
Experimental: Experimental Group 2 (Classical Education)
Students received planned behavior-based hand hygiene education through classical methods.
|
Traditional theory-based hand hygiene training delivered in a classroom setting.
|
|
No Intervention: Control Group
Students received general information about the importance of hand hygiene.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Hygiene Behavior Scale (HBS) Score
Time Frame: Baseline and 3 months post-intervention
|
Evaluation of primary school students' hand hygiene behaviors measured using the Hygiene Behavior Scale.
HBS has 25 items and 3 subscales (personal hygiene subscale (the first 13 items), hand washing subscale (items 14-19), food hygiene subscale (items 20-25)).
Items are scored as 1-Always, 2-Sometimes, 3-Rarely, and 4-Never.
Scores range from [25] to [100], a total of 39 points or above indicates negative hygiene behaviour.
|
Baseline and 3 months post-intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
March 2, 2023
Primary Completion (Actual)
March 7, 2023
Study Completion (Actual)
June 15, 2023
Study Registration Dates
First Submitted
August 25, 2026
First Submitted That Met QC Criteria
August 27, 2026
First Posted (Actual)
August 31, 2026
Study Record Updates
Last Update Posted (Actual)
August 31, 2026
Last Update Submitted That Met QC Criteria
August 27, 2026
Last Verified
August 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 22/11/2022, 349
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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.