NCT06445764

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

50
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Timeline
8mo left

Started Sep 2025

Geographic Reach
1 country

1 active site

Status
withdrawn

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

Study Progress51%
Sep 2025Dec 2026

First Submitted

Initial submission to the registry

May 26, 2024

Completed
11 days until next milestone

First Posted

Study publicly available on registry

June 6, 2024

Completed
1.2 years until next milestone

Study Start

First participant enrolled

September 1, 2025

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 30, 2026

Expected
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

September 26, 2025

Status Verified

July 1, 2025

Enrollment Period

12 months

First QC Date

May 26, 2024

Last Update Submit

September 24, 2025

Conditions

Keywords

in-hospital cardiac arrestEducation, Medical

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

OTHER
Other: e-learning

Virtual reality training

OTHER
Other: Virtual reality training

Interventions

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.

e-learning

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.

Virtual reality training

Eligibility Criteria

Age18 Years - 110 Years
Sexall(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

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.

MeSH Terms

Conditions

Heart Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases
0

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

Locations