Purpose

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.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible 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

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Prevention
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Temporary out-of-home storage (TOHS) training
  • Behavioral: 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

Recruiting Locations

The University of Texas Health Science Center at Houston
Houston 4699066, Texas 4736286 77030
Contact:
Sandra McKay, MD
(713) 500-5666
Sandra.McKay@uth.tmc.edu

More Details

Status
Recruiting
Sponsor
The University of Texas Health Science Center, Houston

Study Contact

Sandra McKay, MD
(713) 500-5666
Sandra.McKay@uth.tmc.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.