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Clinical Trials/NCT06034184
NCT06034184
Recruiting
Not Applicable

To Evaluate Whether Virtual Reality Compared to Standard Education Improves Nursing Students' Ability to Triage in a Simulated Mass Casualty Incident- a RCT

Sophiahemmet University1 site in 1 country100 target enrollmentNovember 8, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Learning
Sponsor
Sophiahemmet University
Enrollment
100
Locations
1
Primary Endpoint
Number of participants performing correct triage
Status
Recruiting
Last Updated
2 years ago

Overview

Brief 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.

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.

Registry
clinicaltrials.gov
Start Date
November 8, 2023
End Date
June 30, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Sophiahemmet University
Responsible Party
Principal Investigator
Principal Investigator

Veronica Lindström

Professor and Registered Nurse

Sophiahemmet University

Eligibility Criteria

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

  • Does not meet inclusion criteria

Outcomes

Primary Outcomes

Number of participants performing correct triage

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

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

Secondary Outcomes

  • Time range on performing correct triage on 10 injured(From enrollment, theoretical education and performing training on mass casualty incidents with or without Virtual Reality)

Study Sites (1)

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