Actively Recruiting
Virtual Reality Lethal Means Safety Training
Led by The University of Texas at Arlington · Updated on 2026-03-04
36
Participants Needed
1
Research Sites
31 weeks
Total Duration
On this page
Sponsors
T
The University of Texas at Arlington
Lead Sponsor
A
American Foundation for Suicide Prevention
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Virtual Reality Lethal Means Safety Training
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 or older
- Healthcare providers serving rural Veterans in Texas (e.g., physicians, physician assistants, nurse practitioners, nurses, pharmacists, social workers, healthcare case managers)
- English-speaking
- Able to provide informed consent
You will not qualify if you...
- Self-reported pregnancy
- History of motor or balance disorders
- Color blindness
- Neurological or cognitive disorders
- Cardiovascular issues that may be worsened by VR use
- Use of cardiac pacemakers, defibrillators, or hearing aids incompatible with VR equipment
- Significant discomfort in virtual reality environments (e.g., severe motion sickness, vertigo)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Texas at Arlington
Arlington, Texas, United States, 76019
Actively Recruiting
Research Team
D
Donna L. Schuman, PhD, LCSW
CONTACT
J
J. SuLynn Mester, DNP, RN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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