NCT07219355

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
5mo left

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress34%
Feb 2026Sep 2026

First Submitted

Initial submission to the registry

September 23, 2025

Completed
28 days until next milestone

First Posted

Study publicly available on registry

October 21, 2025

Completed
4 months until next milestone

Study Start

First participant enrolled

February 23, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2026

Expected
Last Updated

March 4, 2026

Status Verified

February 1, 2026

Enrollment Period

2 months

First QC Date

September 23, 2025

Last Update Submit

March 2, 2026

Conditions

Keywords

VeteransRural VeteransSuicide PreventionSuicide RiskFirearm SafetyMedication SafetyLethal Means Safety CounselingVirtual Reality (VR)VR Training SimulationRural Health

Outcome Measures

Primary Outcomes (1)

  • Confidence in Lethal Means Safety Counseling

    Measured by the Counseling on Access to Lethal Means (CALM) Core Scale (Sale et al., 2018) Confidence subscale ("How confident are you that …"). Items are rated on a 4-point scale and summed; higher scores indicate greater confidence (range = 5 - 20).

    Baseline (pre-test), immediately after intervention (post-test), and 3-month follow-up

Secondary Outcomes (6)

  • Comfortability in Lethal Means Safety Counseling

    Baseline (pre-test), immediately after intervention (post-test), and 3-month follow-up

  • Counseling Intentions

    Baseline (pre-test), immediately after intervention (post-test), and 3-month follow-up

  • Spatial Presence

    Immediately after intervention (post-test only)

  • Engagement

    Immediately after intervention (post-test only)

  • Ecological Validity / Naturalness

    Immediately after intervention (post-test only)

  • +1 more secondary outcomes

Other Outcomes (2)

  • Feasibility of VR Training (Qualitative)

    Immediately after intervention (post-test only)

  • Acceptability (Qualitative)

    Immediately after intervention (post-test only)

Study Arms (2)

VR-LMST Intervention

EXPERIMENTAL

Participants use a Meta Quest 3 headset to complete an interactive virtual reality simulation of a rural clinic visit with a Veteran avatar at risk for suicide. The simulation incorporates skills in suicide risk identification, firearm and medication safety counseling, and collaborative safety planning.

Behavioral: Virtual Reality Lethal Means Safety Training

2D Video Training

ACTIVE COMPARATOR

Participants use a VR headset to view a 10-minute 2D video depicting a lethal means safety counseling session with a veteran.

Behavioral: 2D Video Training

Interventions

A 10-minute video delivered through a VR headset that depicts a healthcare provider conducting lethal means safety counseling with a Veteran. This is a non-interactive training used as an active comparator.

2D Video Training

An immersive behavioral training program delivered through a Meta Quest 3 virtual reality headset. Participants enter a simulated rural health clinic and interact with a Veteran avatar at risk for suicide. The simulation incorporates realistic dialogue and decision points where providers practice skills in suicide risk identification, lethal means safety counseling (firearm and medication storage), and collaborative safety planning. The VR format allows repeated practice in a safe environment and provides a more engaging and realistic training experience than traditional methods.

VR-LMST Intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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 may not qualify if:

  • 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)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Texas at Arlington

Arlington, Texas, 76019, United States

RECRUITING

Related Publications (5)

  • Sale E, Hendricks M, Weil V, Miller C, Perkins S, McCudden S. Counseling on Access to Lethal Means (CALM): An Evaluation of a Suicide Prevention Means Restriction Training Program for Mental Health Providers. Community Ment Health J. 2018 Apr;54(3):293-301. doi: 10.1007/s10597-017-0190-z. Epub 2017 Nov 28.

    PMID: 29185154BACKGROUND
  • Hunter AA, DiVietro S, Boyer M, Burnham K, Chenard D, Rogers SC. The practice of lethal means restriction counseling in US emergency departments to reduce suicide risk: a systematic review of the literature. Inj Epidemiol. 2021 Sep 13;8(Suppl 1):54. doi: 10.1186/s40621-021-00347-5.

    PMID: 34517912BACKGROUND
  • Hoyt T, Holliday R, Simonetti JA, Monteith LL. Firearm Lethal Means Safety with Military Personnel and Veterans: Overcoming Barriers using a Collaborative Approach. Prof Psychol Res Pr. 2021 Aug;52(4):387-395. doi: 10.1037/pro0000372. Epub 2021 May 20.

    PMID: 34421193BACKGROUND
  • Diurba S, Johnson RL, Siry BJ, Knoepke CE, Suresh K, Simpson SA, Azrael D, Ranney ML, Wintemute GJ, Betz ME. Lethal Means Assessment and Counseling in the Emergency Department: Differences by Provider Type and Personal Home Firearms. Suicide Life Threat Behav. 2020 Oct;50(5):1054-1064. doi: 10.1111/sltb.12649. Epub 2020 Jun 29.

    PMID: 32598076BACKGROUND
  • Boggs JM, Quintana LM, Powers JD, Hochberg S, Beck A. Frequency of Clinicians' Assessments for Access to Lethal Means in Persons at Risk for Suicide. Arch Suicide Res. 2022 Jan-Mar;26(1):127-136. doi: 10.1080/13811118.2020.1761917. Epub 2020 May 7.

    PMID: 32379012BACKGROUND

MeSH Terms

Conditions

Suicide, AttemptedSuicide, CompletedSuicide Prevention

Condition Hierarchy (Ancestors)

SuicideSelf-Injurious BehaviorBehavioral SymptomsBehavior

Study Officials

  • Donna L. Schuman, PhD, LCSW

    University of Texas at Arlington, School of Social Work

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Donna L. Schuman, PhD, LCSW

CONTACT

J. SuLynn Mester, DNP, RN

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
Participants and study personnel are aware of assignment because the intervention content differs (interactive VR simulation vs. 2D video). Both groups use headsets to reduce expectancy differences, but this does not blind allocation. To mitigate bias, we use centralized randomization, standardized instructions, and prespecified analyses; where feasible, data analysts will be masked to group labels.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: This is a randomized, parallel-group behavioral clinical trial with two arms. Healthcare providers (≥18, serving Veterans in Texas) are prospectively assigned in a 1:1 ratio to: Intervention (VR-LMST): Participants use a Meta Quest 3 headset to complete an interactive virtual reality simulation of a rural clinic visit with a Veteran avatar at risk for suicide, practicing lethal means safety counseling (firearm and medication storage). Control (2D Video): Participants use the headset to view a 2D, \~10-minute video of the lethal means safety counseling training. Randomization is computer-generated (Excel) with no crossover. Masking is None (Open Label); outcome assessment uses standardized self-report instruments. Surveys are administered pre-intervention, post-intervention, and at 3-month follow-up (e.g., CALM Scale for confidence/comfortability/intentions; ITC-SOPI for presence/engagement/ecological validity/negative effects.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 23, 2025

First Posted

October 21, 2025

Study Start

February 23, 2026

Primary Completion

May 1, 2026

Study Completion (Estimated)

September 30, 2026

Last Updated

March 4, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

This study collects survey and qualitative data from a small sample of healthcare providers. Because of the limited sample size and potential identifiability of responses, individual participant data (IPD) will not be shared. Aggregate data will be shared in publications and presentations.

Locations