NCT07223970RecruitingNot Applicable
Target Safety: a Collaboration of Firearm Retailers and Health Care to Address Suicide Prevention
The University of Texas Health Science Center, Houston1 site in 1 country240 target enrollmentStarted: August 15, 2025Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 240
- Locations
- 1
- Primary Endpoint
- Acceptability of TOHS education as assessed by the likert scale on the post educational survey
Study Overview
Brief Summary
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 Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Prevention
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Gun store owners, firearm range owners, and healthcare providers in the greater Houston area
Exclusion Criteria
- •Non-English or Spanish speakers
Arms & Interventions
Temporary out-of-home storage (TOHS) training
Experimental
Intervention: Temporary out-of-home storage (TOHS) training (Behavioral)
Outcomes
Primary Outcomes
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
Secondary Outcomes
- Appropriateness of the intervention's venue (i.e., location for storage services) as assessed by the post educational survey(post intervention (about 6 weeks after baseline))
- Likelihood to talk to family and friends about TOHS as assessed the post educational survey(post intervention (about 6 weeks after baseline))
- Adoptability of TOHS by firearm owners as assessed by the likert scale on the post educational survey(post intervention (about 6 weeks after baseline))
Investigators
Sandra L. McKay
Associate Professor
The University of Texas Health Science Center, Houston
Study Sites (1)
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