- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06034184
Enhancing Mass Casualty Triage Through Virtual Reality Simulation (VR-MCI-RCT)
December 12, 2023 updated by: Veronica Lindström, Sophiahemmet University
To Evaluate Whether Virtual Reality Compared to Standard Education Improves Nursing Students' Ability to Triage in a Simulated Mass Casualty Incident- a RCT
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.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
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.
Study Type
Interventional
Enrollment (Estimated)
100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Veronica AC Lindström, RN, PhD
- Phone Number: +46703428157
- Email: veronica.lindstrom@shh.se
Study Contact Backup
- Name: Sara Heldring, RN, MSc
- Phone Number: +46707653931
- Email: sara.heldring@shh.se
Study Locations
-
-
-
Stockholm, Sweden, 11428
- Recruiting
- Sophiahemmet University, Lindstedtvägen 8
-
Contact:
- Sara Heldring, RN, MSc
- Phone Number: +46707653931
- Email: sara.heldring@shh.se
-
Contact:
- Mari Lundberg, Professor, PhD
- Phone Number: +4684062091
- Email: mari.lundberg@shh.se
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Principal Investigator:
- Veronica Lindström, Professor, RN, PhD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
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.
|
The nursing students use glasses and handcontrollers (High Fidelity Simulation) in the VR scenario for training and learning mass casualty incidents.
Other Names:
|
No Intervention: Standard education and training
Standard education, including lectures and paper exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
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
|
From enrollment, theoretical education and performing training on mass casualty incidents with or without Virtual Reality
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Time range on performing correct triage on 10 injured
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 time to triage correctly (10 patients) in a simulated MCI situation
|
From enrollment, theoretical education and performing training on mass casualty incidents with or without Virtual Reality
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of participants with correct answers in theoretical tests
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.
|
To measure if VR compared to Standard education has an effect on theoretical knowledge retention
|
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.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Veronica Lindström, PhD, Sophiahemmet University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 8, 2023
Primary Completion (Estimated)
June 30, 2024
Study Completion (Estimated)
June 30, 2024
Study Registration Dates
First Submitted
September 5, 2023
First Submitted That Met QC Criteria
September 5, 2023
First Posted (Actual)
September 13, 2023
Study Record Updates
Last Update Posted (Actual)
December 13, 2023
Last Update Submitted That Met QC Criteria
December 12, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- EPM:2023-02154-02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The data analyzed and presented will be available from the PI and/or corresponding author (when published) on reasonable request
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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