Immersive Virtual Reality Simulation-Effects of Self-Guided Versus Facilitator-Guided Debriefing

Rigshospitalet

Status: Not yet enrolling

Conditions: Debriefing; Pediatric Emergency Medicine; Simulation-based Medical Education; Immersive Virtual Reality; Virtual Reality Simulation

Treatments: Other: Ìmmersive virtual reality simulation with facilitator-guided debriefing; Other: Ìmmersive virtual reality simulation with self-guided debriefing

Study type: Interventional

Funder types: Other

Identifiers

NCT06956833

P-2023-167

Details and patient eligibility

About

The goal of this clinical trial is to find out whether self-guided and facilitator-guided virtual reality (VR) simulations are equally effective in helping medical students learn how to manage and treat critically ill children. The study will also investigate how medical students feel about the two training methods and examine how many experience cybersickness. The main questions it aims to answer are:

• Does self-guided VR simulation work as well as facilitator-guided VR simulation in teaching medical students how to manage critically ill children?
• How do medical students experience the ease of use, workload, reflection on learning, and motivation in each training method?
• How many students experience cybersickness? To answer these questions, researchers will compare the two training methods to evaluate if self-guided VR simulation is an effective way to teach medical students how to manage critically ill children.

Participants will:

• Work through three VR cases to practice managing critically ill children in a safe environment.
• Be tested before and after the VR simulation to assess changes in their skills managing critically ill children.
• Complete surveys about their experience of the VR simulation, the training sessions, and any cybersickness symptoms they might have.

Enrollment: 88 estimated patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Eligible participants will be medical students enrolled at medical schools in Denmark who are within two years of graduation.

Exclusion criteria

• Lack of informed consent

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

---

88 participants in 2 patient groups

Self-guided debriefing

Experimental group

Description:

Immersive virtual reality simulation-based pediatric emergency training with self-guided debriefing

Treatment:

Other: Ìmmersive virtual reality simulation with self-guided debriefing

Facilitator-guided debriefing

Active Comparator group

Description:

Immersive virtual reality simulation-based pediatric emergency training with facilitator-guided debriefing

Treatment:

Other: Ìmmersive virtual reality simulation with facilitator-guided debriefing