The Effect of Preoperative Patient Preparation Video Shown Through Virtual Reality Goggles on Empathy Levels in Nursing Students
PPP-VR
1 other identifier
interventional
50
1 country
1
Brief Summary
This study was planned to evaluate the effect of a preoperative patient preparation video, shown to nursing students via virtual reality glasses, on the development of empathy skills towards the perioperative process.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 25, 2026
CompletedFirst Submitted
Initial submission to the registry
April 27, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 5, 2026
CompletedFirst Posted
Study publicly available on registry
May 7, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 15, 2026
ExpectedMay 7, 2026
February 1, 2026
2 months
April 27, 2026
May 1, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Empathy score
Empathy scores will be measured by the Jefferson Empathy Scale - Health Professions Students Form (JSE-HPS): developed to assess the empathic tendencies of health professions students in a clinical context, and will be used as the primary empathy measurement tool in this study. The scale was developed by Hojat et al. to measure the empathic attitudes of health professionals towards patient care and was later adapted for health professions students. The JSE-HPS is a self-report scale consisting of 7-point Likert-type items that reflect both cognitive and affective components of empathy in a clinical relationship context. 20 items 7-point Likert score range: 20-140 higher score = higher empathy
Time Frame: Baseline; immediately post-intervention; 12th weeks
Secondary Outcomes (1)
Cognitive and affective empathy measured by the Cognitive and Affective Empathy Scale (CAES)
Time Frame: Baseline; immediately post-intervention; 12th weeks
Study Arms (2)
Virtual Realty Video Group
EXPERIMENTALThe students will be taken to an area prepared as a patient room in the simulation laboratory. They will be placed on a bed, playing the role of a patient. They will be shown a 360° pre-operative patient preparation video via VR glasses. The visual content used in the study was recorded with an Insta360 X4 brand 360° action camera. The video includes processes such as identity verification, preoperative evaluation, anesthesia preparation, transfer to the operating room, time-out procedure, etc. The video is approximately 9.5 minutes long. In addition to the VR experience, students in the intervention group will participate in theoretical lectures on the perioperative process, using lecture and question-and-answer methods as outlined in the surgical nursing course curriculum.
Control group
NO INTERVENTIONStudents in the control group will not be included in the VR experience. They will attend only theoretical lectures using lecture and question-and-answer methods on the perioperative process, as outlined in the curriculum.
Interventions
The nursing students in the experimental group 360° pre-operative patient preparation video via VR glasses. The visual content used in the study was recorded with an Insta360 X4 brand 360° action camera. The video includes processes such as identity verification, preoperative evaluation, anesthesia preparation, transfer to the operating room, time-out procedure, etc. The video is 9.5 minutes long.
Eligibility Criteria
You may qualify if:
- Being enrolled in and attending the Surgical Nursing course at the institution where the research is being conducted, and taking the course for the first time
You may not qualify if:
- Having worked or currently working in an operating room.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Acibadem University
Istanbul, Other, 34752, Turkey (Türkiye)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assist. Prof.
Study Record Dates
First Submitted
April 27, 2026
First Posted
May 7, 2026
Study Start
February 25, 2026
Primary Completion
May 5, 2026
Study Completion (Estimated)
June 15, 2026
Last Updated
May 7, 2026
Record last verified: 2026-02