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NCT06113406

Evaluation of Virtual Reality in Hazmat Training

Completed NA Last updated 2 November 2023
What this trial tests

NA trial testing Classroom Training in No Disease or Condition is Being Studied in 15 participants. Completed in 15 June 2023.

Timeline
31 May 2023
Primary endpoint
31 May 2023
15 June 2023

Quick facts

Lead sponsorMetaMedia Training International, Inc.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeother
Enrollment15
Start date31 May 2023
Primary completion31 May 2023
Estimated completion15 June 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

MetaMedia Training International, Inc.

Who can join

Adults 18 to 65, any sex, with No Disease or Condition is Being Studied or Evaluating a Brief Intervention. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06113406.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing