Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07223970

Target Safety: a Collaboration of Firearm Retailers and Health Care to Address Suicide Prevention

Led by The University of Texas Health Science Center, Houston · Updated on 2025-11-03

240

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

T

The University of Texas Health Science Center, Houston

Lead Sponsor

C

Centers for Disease Control and Prevention

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to understand how culturally sensitive messages about safe firearm storage and temporary out-of-home storage (TOHS) are received by firearm owners. The study focuses on suicide prevention by collaborating with firearm retailers and healthcare providers to evaluate this approach. It is an interventional study led by The University of Texas Health Science Center, Houston. The main intervention includes a brief, guided conversation with firearm owners lasting about 5 minutes. During this time, participants discuss their planned storage practices, receive education on secure storage options, and learn about TOHS through a brochure and additional resources. The intervention is behavioral and designed to be conversational and informative. Participants are assessed about 6 weeks after the intervention using surveys that measure how acceptable, appropriate, and adoptable the TOHS education is. The study also evaluates whether participants are likely to discuss TOHS with family and friends. The participation involves a post-educational survey to gather data on these outcomes, with a focus on understanding perceptions and acceptance of the messaging.

CONDITIONS

Brief Title

Target Safety: a Collaboration of Firearm Retailers and Health Care to Address Suicide Prevention

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Gun store owners, firearm range owners, and healthcare providers in the greater Houston area
Not Eligible

You will not qualify if you...

  • Non-English or Spanish speakers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

Duration - Single session lasting up to 5 minutes

Participants receive a brief conversation that includes education on temporary out-of-home firearm storage (TOHS) and secure storage options.

1 visit (in-person)

Follow-up

Duration - About 6 weeks after the baseline session

Participants complete a post-educational survey about 6 weeks after the baseline session to assess acceptability and impact of the TOHS training.

1 follow-up visit (in-person or remote)

Trial Site Locations

Total: 1 location

1

The University of Texas Health Science Center at Houston

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

S

Sandra McKay, MD

K

Kritika Suri

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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