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Supportive Hospital-Based Intervention for Firearm Trauma

Preventing Youth Firearm Violence in New Orleans: A Hospital-Initiated Community Integrated Approach

Who can join

Ages 16 to 24 · All sexes

Inclusion Criteria:

* 16 to 24 years old
* gunshot wound, stab wound, or assault related blunt force trauma injury treated at University Medical Center
* reside in the state of Louisiana
* capacity to provide voluntary informed consent or assent as approved by the Institutional Review Board of Tulane University

Exclusion Criteria:

* not voluntarily agreeing to participate
* not available to participate in study activities in a private room
* age under 16 or over 24
* do not reside in the state of Louisiana
* not acknowledging English as their first language
* being in the judgment of the trauma surgery service as too physically compromised to participate
* intellectual disability as estimated by clinician judgment following mental status examination
* current psychosis as evidenced by structured clinical interview and mental status examination that are administered on as needed basis
* current legal detention status
* injury was a result of intimate partner violence
* does not have the capacity to provide voluntary informed consent or assent as approved by the Institutional Review Board of Tulane University

About the study

This study is a quasi-experimental design, specifically a non-randomized controlled trial (NCT) designed to test the effects of gun violence reduction intervention including MI for youth ages 16-24 years old who present to the Emergency Department or ICU Spirit of Charity Trauma Center (SCTC) at University Medical Centers or another area hospital in New Orleans, Louisiana following a gunshot injury or stab wound. The study will utilize an enrollment strategy that involves alternating, across recruitment days, the assigned study condition. Thus, Day 1 participants would be enrolled into TAU, Day 2 participants would be enrolled in MI-case management condition, Day 3 participants would be enrolled in TAU, etc. This proposed design will minimize any confounds associated with self-selection while possibly increasing enrollment rate.

Research questions include:

1. Will youth allocated to the MI prevention condition have safer firearm related behaviors and beliefs compared to the TAU control condition at 6 months post- enrollment? 2. Will youth allocated to the MI prevention condition have reduced gun violence recidivism compared to the TAU control condition at 18 months post-enrollment. 3. How do youth's social and normative environments influence their gun behaviors and attitudes?

Researchers will compare intervention and TAU arms to see if there are any differences in outcome measures.

Participants will:

1. complete study eligibility assessment, be assigned to one of two conditions depending on the date of assessment, consent, and enroll in the Emergency Department (ED) or inpatient unit of hospital by a study team member, 2. participate in one of two conditions: MI administered by a licensed clinical social worker, or treatment as usual control group (TAU) administered by a study team member (n=170 per condition) 3. complete three surveys (baseline, 3-month, and 6-month) conducted by a study team member 4. 18-month post examination of participant hospital records 5. have the option to complete a 1-1.5 hour interview, 1-3 months after the 6-month survey is completed (n=50)

What is being tested

• Motivational Interviewing and Firearm Safety Training, with Case Management (behavioral)

Sponsor: Tulane University · Participants: 350 · Started: Aug 31, 2022

Contact the study team

• Julia M Fleckman, PHD, MPH · Phone: 504-988-9937

Official record on ClinicalTrials.gov — NCT06712940

Locations in the U.S.

Conditions

• Teen Violence

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.