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A Virtual Reality Brief Violence Intervention: Preventing Gun Violence Among Violently Injured Adults

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 11 months later Sep 2026 → Sep 29, 2027
See other at-risk trials from Virginia Commonwealth University

Record History

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  1. Primary completion pushed from Sep 2026 to Sep 29, 2027 Show 4 more changesShow less
    • Primary endpoints: details revised at 3 of 4 entries
    • Study completion pushed from Oct 2026 to Oct 2027
    • Secondary endpoints: details revised at 3 of 3 entries
    • Eligibility criteria expanded, about 5 words
  2. 2 versions Re-verified since Jun 6, 2025, no change to tracked fieldsv4-v5
  3. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of May 2024 to Feb 26, 2024
    • Site details revised
    v3
  4. Re-verified, no change to tracked fieldsv2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The overall aim of the proposed project is to develop and evaluate the effectiveness of Brief Violence Intervention-Virtual Reality (BVI-VR) for reducing firearm-related violence, re-injury, and mortality among victims of violence. Outcome measures of firearm-related violence will come from multiple sources, including criminal background checks, hospital data, state-level data, semi-structured clinical assessments, and self-report assessments. In addition, the study aims to understand the impact of BVI-VR on psychosocial mediators resulting in a reduction of firearm-related violence. This will include self-report surveys, neurocognitive assessments, and clinical assessments. The economic efficiency of BVI-VR as a firearm-related violence intervention will also evaluated. To achieve these aims, a randomized control trial (RCT) in a large sample of violently injured adults (18+ years) from VCU Health will be conducted.
Trial Details
NCT Number NCT06239285
Lead Sponsor Virginia Commonwealth University
Collaborators: Centers for Disease Control and Prevention
Conditions
(from sponsor)		 Violence
Enrollment 220 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov