Virtual Reality-Based Simulation Versus High-Fidelity Simulation for Emergency Management Training in Medical Interns

NCT07584863 — Not applicable, Active not recruiting, 124 participants, Seoul National University Hospital

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A Randomized Controlled Study Comparing Virtual Reality-Based Simulation With High-fidelity Simulation for Training Novice Physicians in Emergency Management

RegistryNCT07584863
StatusActive not recruiting
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: single, other
Enrollment124 (Estimated)
SponsorSeoul National University Hospital (Other)
ConditionsAnaphylaxis, Hypoxia
InterventionsVirtual Reality-Based Emergency Simulation, High-Fidelity Simulation (Behavioral)
Datesstart 2026-02-20, primary completion 2027-12-31 (estimated), completion 2027-12-31 (estimated), first posted 2026-05-13, last updated 2026-05-13
Locations1 site in South Korea

Related Papers Related Patents Related Grants Related Experts
All trials for Anaphylaxis All trials for Hypoxia All trials of Virtual Reality-Based Emergency Simulation All trials of High-Fidelity Simulation

-Summary

This study is a two-arm parallel randomized controlled non-inferiority trial designed to compare the educational effectiveness of virtual reality (VR)-based simulation with high-fidelity simulation (HFS) for emergency management training in medical interns.

Participants will be randomized 1:1 to either VR-based training or HFS-based training for managing desaturation and anaphylaxis scenarios. After training and structured debriefing, all participants will undergo objective structured clinical examinations (OSCEs) and complete pre- and post-training surveys.

The primary outcome is OSCE performance score. Secondary outcomes include confidence improvement, participant satisfaction, usability (UEQ-S).

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+Arms and interventions

ArmTypeInterventionsDescription
VR GroupExperimentalBehavioral: Virtual Reality-Based Emergency SimulationParticipants use an immersive VR platform to manage simulated patients with oxygen desaturation and anaphylaxis.
HFS GroupActive comparatorBehavioral: High-Fidelity SimulationParticipants use a high-fidelity simulator (Sim-Man) to manage the same emergency scenarios.
  • Virtual Reality-Based Emergency Simulation (Behavioral): Participants use an immersive VR platform to manage simulated patients with oxygen desaturation and anaphylaxis.
  • High-Fidelity Simulation (Behavioral): Participants use a high-fidelity simulator (Sim-Man) to manage the same emergency scenarios.

+Outcome measures

Primary outcomes

  • OSCE Performance Score [Immediately after training]: Mean total score of two Objective Structured Clinical Examination (OSCE) stations (desaturation and anaphylaxis). Scores range from 0 to 20, with higher scores indicating better clinical performance.

Secondary outcomes

  • Confidence Improvement [Immediately before and immediately after training]: Self-reported confidence in emergency management measured using a 10-point Likert scale ranging from 1 to 10, with higher scores indicating greater confidence.
  • Participant Satisfaction [Immediately after training]: Participant satisfaction measured using a 7-point Likert scale ranging from 1 to 7, with higher scores indicating greater satisfaction.
  • Usability (UEQ-S) [Immediately after training]: Usability assessed using the User Experience Questionnaire-Short Version (UEQ-S). Scores range from 1 to 7, with higher scores indicating a more positive user experience.

Other outcomes

  • Task Completion Time [Immediately after training]: Time required to complete VR emergency scenarios, measured in seconds.
  • Critical Action Completion Rate [Immediately after training]: Percentage of predefined critical actions successfully completed during VR scenarios.
  • Task Sequence Accuracy [Immediately after training]: Accuracy of procedural task sequence during VR emergency scenarios based on predefined scenario flow.

+Eligibility

Sex: All, accepts healthy volunteers

Inclusion Criteria

* Medical interns enrolled in the 2026 internship program at Seoul National University Hospital
* Provided written informed consent

Exclusion Criteria

* Did not complete pre-training survey
* Declined participation

+Locations (1)

FacilityCityCountryStatus
Seoul National University HospitalSeoul, SeoulSouth Korea

+Investigators

  • Sun Jung Myung, Principal investigator, Seoul National University Hospital