Educational Efficacy of VR vs. Simulator in Emergency Medical Training
Development, Application, and Educational Efficacy of Medical Education Program Using Virtual Reality Technology
1 other identifier
interventional
166
0 countries
N/A
Brief Summary
It has not been revealed which is more effective: an education program using virtual reality technology or a simulation education program using Sim-man. In this study, the participants are new doctors who graduated from medical school and started working as interns at hospitals. The participants were divided into two groups. One group received a training program using virtual reality technology, and the other group received simulation training using Sim-man. The investigators would like to compare the increase in confidence and satisfaction before and after training. After the classes and surveys are completed for each group, the participants will be able to receive other educational methods if they wish.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Apr 2024
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 13, 2024
CompletedFirst Posted
Study publicly available on registry
March 6, 2024
CompletedStudy Start
First participant enrolled
April 13, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 28, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedMarch 8, 2024
March 1, 2024
11 months
February 13, 2024
March 6, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
self-rated confidence for managing emergency situation
self-rated confidence survey (10-Likert scale) for managing emergency situation: "I am confident in managing desaturation patients" 1: strongly disagree, 10: strongly agree
1 hour after education program
self-rated confidence for managing emergency situation
self-rated confidence survey (10-Likert scale) for managing emergency situation: "I am confident in managing desaturation patients" 1: strongly disagree, 10: strongly agree
6 months after starting intern training
performance in managing emergency situation
Objective Structured Clinical Examination for physician's performance in managing emergency situation
1 week after education program
Secondary Outcomes (3)
usability of Virtual Reality simulation program using User Experience Questionnaire Short
1hour after education program
usability of Virtual Reality simulation program using Simulator Sickness Questionnaire
1hour after education program
usability of Virtual Reality simulation program using System Usability Scale
1hour after education program
Study Arms (2)
Test group
EXPERIMENTALThe test group wears an HMD (head-mounted display) and participates in a simulation program using VR. They experience both easy and difficult cases using VR. After the simulation session, a debriefing session will be provided.
Control group
ACTIVE COMPARATORThe control group participates in simulation training using Sim-man, and the scenarios are the same in both the control and the test groups (easy cases and difficult cases). After the simulation session, a debriefing session will be provided.
Interventions
Simulation program using VR or simulator that mimics patient's desaturation
Eligibility Criteria
You may qualify if:
- the medical interns who participate in the education program for medical interns, who will work as interns at Seoul National University Hospital from March 2024
- participants who agree to the purpose of the study and consent to participation
You may not qualify if:
- who do not consent to participate in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Seoul National University Hospitallead
- Seoul National Universitycollaborator
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
- Professor
Study Record Dates
First Submitted
February 13, 2024
First Posted
March 6, 2024
Study Start
April 13, 2024
Primary Completion
February 28, 2025
Study Completion
December 31, 2025
Last Updated
March 8, 2024
Record last verified: 2024-03