CClinicalTrials.gg
CompletedNCT06034184VR-MCI-RCTUpdated May 19, 2026

Enhancing Mass Casualty Triage Through Virtual Reality Simulation

An interventional study of Virtual Reality in Learning, Mass Casualty Incident and Triage, sponsored by Sophiahemmet University. Completed at 1 site in Sweden. Per ClinicalTrials.gov, last updated 2026-05-19.

Sponsored by Sophiahemmet University · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Sex
All
01

Study summary

This interventional study aims to investigate whether Virtual Reality (VR) compared to traditional education and training, can enhance the correct triage abilities of nursing students in simulated mass casualty incidents (MCI). The primary research question seeks to answer if VR compared to Standard education supports students' ability to triage correctly in a simulated MCI situation. Additionally, this study aims to address the following secondary questions: Does VR compared to standard education have an effect on the time to triage in a simulated MCI situation? And, does VR compared to Standard education have an effect on theoretical knowledge retention concerning triage in MCI situations? In the interventional group, participants will utilize VR for MCI training and learning, while the control group will undergo standard education, including lectures and paper exercises. The researchers will compare the two groups of nursing students to assess whether VR yields better outcomes in MCI triage education.

Read the detailed description

A randomized controlled trial (RCT) involving nursing students from a university in Stockholm, Sweden. The students are randomly allocated in a 1:1 ratio to either VR (intervention) or standard training in triaging during a mass casualty Incident. Both groups of participants will receive the same lecture on disaster events and triage using the same method before undergoing triage training either with VR support or traditional paper-based training. To achieve a power of 0.80 and a p-value of 0.05, a total of 60 participants are required (control n=30, intervention n=30). However, all students (approximately 100) will be invited to participate in the study to avoid excluding those who wish to take part in the study. The primary outcome measure is the students' ability to triage correctly. Secondary outcome measures include knowledge and knowledge retention, as well as the time taken to triage correctly. Knowledge tests will be conducted approximately one week after training and again 3-6 months after completing the training. The knowledge test consists of a questionnaire with 20 multiple-choice questions used in previous studies.

02

Conditions studied

  • Learning
  • Mass Casualty Incident
  • Triage
  • Training

Keywords

  • Virtual Reality
  • Mass casualty incidents
  • Triage
  • Learning
  • Nursing Students
03

In context

Lead sponsor

Sophiahemmet University is the lead sponsor of 9 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

Nursing students registered for a course in disaster medicine/emergency care that is conducted during their fifth semester (out of 6) in the nursing program.

Exclusion criteria

Exclusion Criteria:

Does not meet inclusion criteria

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
100 participants (actual)

Study arms

  • Experimental
    Using Virtual Reality for training and learning mass casualty incidents

    The nursing students use glasses and handcontrollers (High Fidelity Simulation) in the VR scenario for training and learning mass casualty incidents.

    Other: Virtual Reality

  • No intervention
    Standard education and training

    Standard education, including lectures and paper exercises

Interventions

  • OtherVirtual Reality

    The nursing students use glasses and handcontrollers (High Fidelity Simulation) in the VR scenario for training and learning mass casualty incidents.

    Also known as: Training mass casualty incidents

06

What researchers measure

Primary outcomes

  1. Number of participants performing correct triage

    Measuring if VR compared to Standard education has an effect on the frequency of correctly triage

    Time frame: From enrollment, theoretical education and performing training on mass casualty incidents with or without Virtual Reality

Secondary outcomes

  1. Time range on performing correct triage on 10 injured

    Measuring if VR compared to Standard education has an effect on the time to triage correctly (10 patients) in a simulated MCI situation

    Time frame: From enrollment, theoretical education and performing training on mass casualty incidents with or without Virtual Reality

Other outcomes

  1. Number of participants with correct answers in theoretical tests

    To measure if VR compared to Standard education has an effect on theoretical knowledge retention

    Time frame: From enrollment, the training on mass casualty incidents with or without Virtual Reality and measuring nursing students theoretical knowledge retention on triage 1 week- 3-6 months after training.

07

Study locations

1 site
  • Sophiahemmet University, Lindstedtvägen 8
    Stockholm, Stockholm County 11428, Sweden
08

References and documents

Individual participant data

Plan to share: No — The data analyzed and presented will be available from the PI and/or corresponding author (when published) on reasonable request

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 19, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06034184
Lead sponsor
Sophiahemmet University
Collaborators
Falck Ambulance A/S, CrashCourse AB, Laerdal Medical Foundation, Ambulance Service in Stockholm, Sweden (AISAB)
Responsible party
Veronica Lindström (Professor and Registered Nurse, Sophiahemmet University) — Principal investigator
First posted
Sep 13, 2023
Start date
Nov 8, 2023
Primary completion
Oct 24, 2024
Completion
Oct 24, 2024
Last update
May 19, 2026

Study contacts

Veronica Lindström, PhD
principal investigator · Sophiahemmet University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2023. You cannot join it, but the record below documents what was studied.

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