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Launching the Houston Hospital-Based Violence Intervention Program (Houston-HVIP): Developing and Evaluating a Hospital-Based Intervention to Reduce Recurrent Violence

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Enrolling

Conditions

Firearm Injury

Treatments

Behavioral: Standard of Care
Behavioral: Houston-HVIP treatment

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06263647
UH3NR021232 (U.S. NIH Grant/Contract)
HSC-MS-23-0904
UG3NR021232 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

A prior violent injury is one of the strongest predictors of future violent injury, highlighting the importance of effective hospital-based interventions to prevent reinjury. This project will establish and evaluate the Houston Hospital-Based Violence Intervention Program (Houston-HVIP). Using a randomized controlled trial, the study will assess the effectiveness of Houston-HVIP in reducing violent reinjury and improving behavioral, mental, and physical health outcomes over a 12-month follow-up period among those enrolled in the study in ages 16-35 years of age.

Enrollment

274 estimated patients

Sex

All

Ages

16 to 35 years old

Volunteers

No Healthy Volunteers

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

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

274 participants in 2 patient groups

Houston-HVIP treatment group
Experimental group
Treatment:
Behavioral: Houston-HVIP treatment
Standard of Care group
Active Comparator group
Treatment:
Behavioral: Standard of Care

Trial contacts and locations

1

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Central trial contact

Sandra McKay, MD; Alexander Testa, PhD

Data sourced from clinicaltrials.gov

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