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NCT06712940 · ClinicalTrials.gov registry record · NA

Supportive Hospital-Based Intervention for Firearm Trauma

A NA study of Adolescent Behavior and Gun Violence Prevention, sponsored by Tulane University.

Recruiting
Registry status
NA
Development phase
350
Enrollment target
1
Study location

NCT06712940: Recruiting NA study of Adolescent Behavior and Gun Violence Prevention, sponsored by Tulane University.

NCT06712940 is a NA study of Adolescent Behavior and Gun Violence Prevention that is actively recruiting participants, run by Tulane University. The registered enrollment target is 350 participants, roughly in line with the 322-participant average among 46 other Adolescent Behavior trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06712940, a NA study of Adolescent Behavior and Gun Violence Prevention, is actively recruiting participants, sponsored by Tulane University.

RECRUITING
Registry status
NA
Development phase
350 participants
Enrollment target
1
Study location

Study Summary

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

Primary Outcome

Frequency of firearm carriage outside of home

Interventions

  • BEHAVIORAL Motivational Interviewing and Firearm Safety Training, with Case Management

Study Locations (1)

Louisiana

  • Tulane School of Public Health and Tropical Medicine - New Orleans

Trial Details

FieldValue
Enrollment Target 350 participants
Start Date 2022-08-31
Est. Completion 2028-03-30
Phase NA
Tulane University

73 total trials

What NCT06712940 shows while recruiting

NCT06712940 is an interventional study that assigns participants to a tested intervention. The registered 350 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 322-participant average among 46 other Adolescent Behavior trials with a reported enrollment target.

The record links to 2 conditions, with Adolescent Behavior appearing as the primary indexed condition, and to 1 intervention - of which Motivational Interviewing and Firearm Safety Training, with Case Management is the first listed.

NCT06712940 reports a single indexed study location in Louisiana.

Frequently Asked Questions

What is clinical trial NCT06712940 about?

NCT06712940 is a clinical study titled "Supportive Hospital-Based Intervention for Firearm Trauma". 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 Uni...

What is the current status of trial NCT06712940?

This trial is currently recruiting. It is a NA study. The enrollment target is 350 participants. The study started on 2022-08-31. Estimated completion is 2028-03-30.

What conditions does trial NCT06712940 study?

This clinical trial studies the following conditions: Adolescent Behavior, Gun Violence Prevention.

What interventions are being tested in trial NCT06712940?

The interventions under investigation include: Motivational Interviewing and Firearm Safety Training, with Case Management (BEHAVIORAL).

Who is sponsoring clinical trial NCT06712940?

This trial is sponsored by Tulane University, which has 73 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06712940 being conducted?

This trial has 1 study location across Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Adolescent Behavior

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06712940's enrollment target sits among peer trials

350 10th of 46 higher than 37 of 46 other Adolescent Behavior trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Adolescent Behavior trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06712940, the US trial registry maintained by the National Library of Medicine. NCT06712940 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.