Study Stopped
Technical problems with VR scenario development
Traumatic Cardiac Arrest and Trauma SimVR Training
Trauma SimVR
Enhancing Trauma Cardiopulmonary Resuscitation Simulation Training With the Use of Virtual Reality (Trauma SimVR): Protocol for a Randomized Controlled Trial
1 other identifier
interventional
N/A
1 country
1
Brief Summary
The goal of this single-center, prospective, randomized, controlled trial is to evaluate the effectiveness of using virtual reality technology to provide learners with skills and knowledge in the management of traumatic cardiac arrest in first-year residents at the emergency department. The main question it aims to answer is: Does the use of virtual reality in the context of trauma cardiopulmonary resuscitation training result in shorter times to order/perform pre-defined critical actions? Participants will learn management skills for in-hospital traumatic cardiac arrest using either newly developed virtual reality software or e-learning focused on the same content.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Sep 2025
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
First Submitted
Initial submission to the registry
May 26, 2024
CompletedFirst Posted
Study publicly available on registry
June 6, 2024
CompletedStudy Start
First participant enrolled
September 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
September 26, 2025
July 1, 2025
12 months
May 26, 2024
September 24, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Time to critical action
Expert-based assessment of the difference in time (seconds) to the predefined primary critical action between randomized groups in video recordings of an in-person assessment simulation.
evaluation within 4 weeks after study completion
Secondary Outcomes (25)
Time to secondary critical action #1
evaluation within 4 weeks after study completion
Time to secondary critical action #2
evaluation within 4 weeks after study completion
Number of unrecognized causes of traumatic cardiac arrest
evaluation within 4 weeks after study completion
Number of patients declared dead prematurely
evaluation within 4 weeks after study completion
Number of protocol deviations
evaluation within 4 weeks after study completion
- +20 more secondary outcomes
Study Arms (2)
e-learning
OTHERVirtual reality training
OTHERInterventions
Participants will complete an e-learning course over a two-week period that focuses on skills and knowledge related to the management of in-hospital cardiac arrest. This course prepares participants for an in-person assessment.
Participants will complete a virtual reality training over a two-week period that focuses on skills and knowledge related to the management of in-hospital cardiac arrest. This training prepares participants for an in-person assessment.
Eligibility Criteria
You may qualify if:
- first-year residents at the emergency department
- only people who do not need eyeglasses for using VR
You may not qualify if:
- \- pre-disposition for cybersickness (motion sickness, pregnancy, pre-existing cybersickness)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Medical University of Vienna
Vienna, 1090, Austria
Related Publications (1)
Lintschinger JM, Metelka P, Kapral L, Kahlfuss F, Reischmann L, Kaider A, Holaubek C, Kaiser G, Wagner M, Ettl F, Sixt L, Schaden E, Hafner C. Enhancing trauma cardiopulmonary resuscitation simulation training with the use of virtual reality (Trauma SimVR): Protocol for a randomized controlled trial. PLoS One. 2025 Jan 24;20(1):e0316828. doi: 10.1371/journal.pone.0316828. eCollection 2025.
PMID: 39854477DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
May 26, 2024
First Posted
June 6, 2024
Study Start
September 1, 2025
Primary Completion (Estimated)
August 30, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
September 26, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share