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

October 30, 2025 updated by: Sandra L. McKay, The University of Texas Health Science Center, Houston
The purpose of the study is to understand how culturally competent messaging on secure firearm storage and temporary out-of-home storage (TOHS) is perceived and accepted by firearm owners.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

240

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Gun store owners, firearm range owners, and healthcare providers in the greater Houston area

Exclusion Criteria:

  • Non-English or Spanish speakers

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Temporary out-of-home storage (TOHS) training
The intervention will consist of a brief conversation with the firearm owner, which will include asking about their planned storage practices, providing education on secure storage options, assessing their knowledge about TOHS, and providing subsequent education about TOHS. The intervention is designed to be brief and conversational, taking no more than 5 minutes. The conversation will be guided by a brochure developed by our expert team, and firearm owners will be directed to additional resources for further information

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Acceptability of TOHS education as assessed by the likert scale on the post educational survey
Time Frame: post intervention (about 6 weeks after baseline)
The survey will be reported categorically as Not at all, Slightly, Moderately, Very, and Extremely
post intervention (about 6 weeks after baseline)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Appropriateness of the intervention's venue (i.e., location for storage services) as assessed by the post educational survey
Time Frame: post intervention (about 6 weeks after baseline)
There are 3 questions and each is reported categorically as yes or no
post intervention (about 6 weeks after baseline)
Likelihood to talk to family and friends about TOHS as assessed the post educational survey
Time Frame: post intervention (about 6 weeks after baseline)
This is a 2 item questionnaire and each will be categorically reported as yes or no
post intervention (about 6 weeks after baseline)
Adoptability of TOHS by firearm owners as assessed by the likert scale on the post educational survey
Time Frame: post intervention (about 6 weeks after baseline)
This will be reported categorically as Strongly Disagree, Disagree, Neutral, Agree or Strongly Agree
post intervention (about 6 weeks after baseline)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sandra McKay, MD, The University of Texas Health Science Center, Houston

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 15, 2025

Primary Completion (Estimated)

January 30, 2026

Study Completion (Estimated)

January 30, 2026

Study Registration Dates

First Submitted

October 30, 2025

First Submitted That Met QC Criteria

October 30, 2025

First Posted (Estimated)

November 3, 2025

Study Record Updates

Last Update Posted (Estimated)

November 3, 2025

Last Update Submitted That Met QC Criteria

October 30, 2025

Last Verified

October 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • HSC-MS-25-0401

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Firearm Injury

Clinical Trials on Temporary out-of-home storage (TOHS) training

Subscribe