Houston Hospital-Based Violence Intervention Program to prevent repeat firearm injuries
Official title: Launching the Houston-HVIP: Developing and Evaluating a Hospital-Based Intervention to Reduce Recurrent Violence
Run by The University of Texas Health Science Center, Houston · NCT06263647 · Data updated 2026-11-12
This project will test whether a hospital-based violence intervention (Houston-HVIP) can reduce repeat firearm injuries and improve mental, behavioral, and physical health over 12 months in people ages 16–35 treated for gunshot wounds.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 16 Years to 40 Years |
| Sex | All |
| Enrollment | 274 (estimated) |
| Sponsor | The University of Texas Health Science Center, Houston Academic / other |
| Locations | 1 site (Houston, Texas) |
| Status | Recruiting |
| Started | September 16, 2025 |
| Main results expected | February 1, 2028 |
| Study ends | May 31, 2028 |
| Registry record updated | October 16, 2026 |
| Trial ID | NCT06263647 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are English- or Spanish-speaking people aged 16–35 who live in Harris County and present to Memorial Hermann Hospital with a gunshot injury from community violence and can give voluntary consent.
✕Probably not a fit
Patients whose injuries were self-inflicted or accidental, those who are actively detained, or people who do not live in Harris County or cannot consent are unlikely to qualify or benefit from this program.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized controlled trial will enroll patients aged 16–35 who present to Memorial Hermann Hospital with gunshot injuries from community violence and who live in Harris County. Participants who consent and speak English or Spanish will be randomly assigned to receive the Houston-HVIP intervention or standard of care. The study will track violent reinjury and a range of behavioral, mental health, and physical recovery outcomes over a 12-month follow-up. Exclusions include self-inflicted or unintentional firearm injuries and patients actively detained by the criminal justice system at enrollment.
Why it matters
Potential benefit: If successful, the program could lower the chance of repeat firearm injury and support better mental and physical recovery after a violent injury.
How similar studies have gone: Similar hospital-based violence intervention programs have shown promising reductions in repeat injury and related harms in several prior trials, although results vary by setting.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * presented for a gunshot injury stemming from community violence at Memorial Hermann Hospital * English or Spanish-speaking * provide informed voluntary consent to participate in the study * live in Harris County at time of enrollment * live within 40-mile radius of Memorial Hermann Hospital- Texas Medical Center Exclusion Criteria: * presenting for a firearm injury arising from a self-inflicted gunshot or unintentional gun violence * actively detained by criminal justice systems at time of enrollment
Where it's running
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The University of Texas Health Science Center at Houston
Houston, Texas, United States Recruiting
Study contacts
- Principal investigator: Sandra McKay, MD — The University of Texas Health Science Center, Houston
- Study coordinator: Sandra McKay, MD
- Email: Sandra.McKay@uth.tmc.edu
- Phone: (713) 500-5666
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Recovery Legal Care: a program to help firearm-injury patients through legal support
This trial tests a medical-legal partnership that connects legal help with hospital-based violence recovery to address social and economic risks for patients treated for firearm or other violent injuries.
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Evaluation of a hospital violence intervention program
This study is testing a program designed to help young people aged 16-35 who have experienced violence to see if it can reduce repeat injuries, improve their mental health, and enhance their overall hospital experience.
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Program to prevent youth gun violence in Washington D.C.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.