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

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07223970
Enrollment
310
Registered
2025-11-03
Start date
2025-08-15
Completion date
2026-05-30
Last updated
2026-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Firearm Injury, Suicide Due to Use of Firearm

Keywords

temporary out-of-home storage (TOHS).

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.

Interventions

BEHAVIORALTemporary 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

Sponsors

The University of Texas Health Science Center, Houston
Lead SponsorOTHER
Centers for Disease Control and Prevention
CollaboratorFED

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

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

Secondary

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

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORSandra McKay, MD

The University of Texas Health Science Center, Houston

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 16, 2026