- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07223970
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
Status
Recruiting
Conditions
Intervention / Treatment
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
- Name: Sandra McKay, MD
- Phone Number: (713) 500-5666
- Email: Sandra.McKay@uth.tmc.edu
Study Contact Backup
- Name: Kritika Suri
- Phone Number: (713) 500-5580
- Email: Kritika.Suri@uth.tmc.edu
Study Locations
-
-
Texas
-
Houston, Texas, United States, 77030
- Recruiting
- The University of Texas Health Science Center at Houston
-
Contact:
- Sandra McKay, MD
- Phone Number: (713) 500-5666
- Email: Sandra.McKay@uth.tmc.edu
-
Contact:
- Kritika Suri
- Phone Number: (713) 500-5580
- Email: Kritika.Suri@uth.tmc.edu
-
-
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.
Collaborators
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.
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