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Study identifier: NCT07219355 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Virtual Reality Lethal Means Safety Training

Condition: Suicide, Attempted · Suicide, Completed · Suicide Prevention  ·  Sponsor: The University of Texas at Arlington

PhaseNA
Planned participants36
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

The goal of this randomized clinical trial is to determine whether a virtual reality (VR) training program can help healthcare providers improve their skills in discussing suicide prevention and safe storage of firearms and medications with Veterans. The study will test whether VR training increases providers' self-efficacy, confidence, and comfort in conducting lethal means safety counseling, and whether it improves their intention to use these counseling practices in their clinical work. Researchers will compare healthcare providers who complete the VR training to those who complete a 2D video training to determine whether the VR approach is more effective. Participants will complete online surveys before and after the training and again three months later. They will be randomly assigned to one of two groups: VR training group: Participants use a VR headset to interact with a virtual Veteran patient in a simulated rural clinic and practice suicide prevention counseling skills; Video training group: Participants use the same headset to watch a \~10-minute 2D video depicting the lethal means safety counseling session. After the training, participants will also provide feedback about their experience, including how realistic and useful they found the training.

This description comes directly from the study's public registry record.

Talk to the study team

Donna L. Schuman, PhD, LCSW  ·  817-272-3181  ·  donna.schuman@uta.edu

J. SuLynn Mester, DNP, RN  ·  sulynn.mester@uta.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Texas at ArlingtonArlington, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07219355