Comparing self-guided and facilitator-guided virtual reality training for medical students
Self-Guided Versus Facilitator-Guided Debriefing in Immersive Virtual Reality Simulation: Protocol for a Randomized Controlled Non-Inferiority Trial As-sessing Teamwork Skills in Medical Students
This study tests whether medical students learn better to manage critically ill children using self-guided virtual reality training or training led by a facilitator.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 88 (estimated) |
| Sex | All |
| Sponsor | Rigshospitalet, Denmark Academic / other |
| Locations | 1 site (Copenhagen) |
| Trial ID | NCT06956833 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of self-guided versus facilitator-guided immersive virtual reality simulations in teaching medical students how to manage critically ill children. Participants will engage in three virtual reality cases and provide feedback on their experiences, including ease of use, workload, and motivation. The study will also assess the incidence of cybersickness among students during the training. By comparing these two methods, the research seeks to determine if self-guided simulations can be as effective as those guided by a facilitator.
Who should consider this trial
Good fit: Ideal candidates for this study are medical students in Denmark who are within two years of graduation.
Not a fit: Patients who may not benefit from this study include those who are not medical students or who are not enrolled in a medical program.
Why it matters
Potential benefit: If successful, this study could enhance medical education by providing effective training methods for managing pediatric emergencies.
How similar studies have performed: Other studies have shown promise in using virtual reality for medical training, suggesting that this approach could be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Copenhagen
- Copenhagen University Hospital, Rigshospitalet — Copenhagen, Denmark (Recruiting)
Study contacts
- Study coordinator: Amalie M Andersen, MD, PhD student
- Email: amalie.middelboe.andersen@regionh.dk
- Phone: 25344610
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.