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Evaluation of Virtual Reality in Hazmat Training

Evaluation of Virtual Reality in Hazmat Training

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06113406
Enrollment
15
Registered
2023-11-02
Start date
2023-05-31
Completion date
2023-06-15
Last updated
2023-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Does Virtual Reality Aid in Hazmat Training, Evaluating a Brief Intervention, No Disease or Condition is Being Studied

Brief summary

Type of study: Two-group comparison. Main question it aims to answer: Does the use of virtual reality emergency scenarios provide a practical and effective tool to supplement traditional instructor-led training for first responder trainees? A. For the traditional hazmat response training group; Traditional training will be held in the classroom environment for 45 minutes in the form of a lecture, then the training session will be terminated. B. For VR hazmat response training group; After the traditional classroom session has ended, the participants will complete the additional VR training scenario, online content, and question-answer session. Once completed the session will be closed.

Interventions

Active Comparator

BEHAVIORALVirtual Reality Training

Experimental

Sponsors

MetaMedia Training International, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Masking description

The person who will make the statistical analysis does not know which group the participants in our study belong to and does not know the participants.

Intervention model description

An experimental and a pretest-posttest control group design method were applied in this regard.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* currently enrolled in a hazmat training course

Exclusion criteria

* under the age of 18 or over the age of 65

Design outcomes

Primary

MeasureTime frameDescription
Keywords identified on questionnaireday 1Participants will receive a score of zero to ten based on the number of keywords they identified. Each correct key word identified is worth 1 point. Minimum 0, maximum 10 points can be scored. Higher scores mean a better outcome.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026