Recruiting

BeSMARTBeSMART Secure Firearm and Medication Storage Education for Inpatients

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Study Aim

This study aims to educate hospital patients on secure firearm and medication storage to assess changes in their storage behaviors and asking practices about firearms in homes.

What is being tested

Safe Storage Intervention

+ Safe Kids Medication

Behavioral
Who is being recruted

Over 18 Years
See all eligibility criteria
How is the trial designed

Other Study

Interventional
Study Start: September 2025
See protocol details

Summary

Principal SponsorVanderbilt University Medical Center
Study ContactKelsey Gastineau, MD, MPHMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 20, 2025

Actual date on which the first participant was enrolled.

This study aims to explore the effectiveness of providing education on securely storing firearms and medications in homes, especially focusing on families with children. It involves participants who are both gun owners and non-gun owners, ensuring a balanced representation in the study. The goal is to help prevent accidents and intentional harm, such as suicide, by educating families on the benefits of proper storage practices. This research is important as it addresses a significant safety concern in households and aims to reduce injuries and fatalities related to improper storage of guns and medications. Participants in this study are randomly assigned to two groups. One group receives the Be SMART intervention, which includes watching a short video about secure firearm storage, and they are offered a cable gun lock for safe storage. The other group watches a video about medication storage safety. Both groups receive this information via a tablet during their initial visit, and they complete a survey immediately after. Follow-up surveys are conducted electronically or via phone at one month and three months after the initial session to assess the impact of the interventions. Clinicians are available to answer any questions participants might have, ensuring they fully understand the safety practices being promoted.

Official TitleBeSMART Secure Storage Counseling in the Inpatient Setting
Principal SponsorVanderbilt University Medical Center
Study ContactKelsey Gastineau, MD, MPHMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

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

400 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other Study

Some studies explore topics that don't fall into a specific category. These might include innovative research, new technologies, or emerging healthcare areas.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

Inclusion Criteria (must meet ALL): 1. Provision of signed and dated informed consent form 2. Caregiver of child hospitalized on a pediatric hospital medicine service aged 0-17 3. English or Spanish speaking caregiver 4. Access to necessary resources for participating in a technology-based intervention follow-up assessments (e-mail and telephone) Exclusion Criteria: 1. Caregivers of children admitted for firearm injury 2. Caregivers of children with a firearm injury within the last 3 months 3. Caregivers of children admitted with a primary psychiatric diagnosis including suicidal ideation, self-harm, homicidal ideation, aggression, or intentional ingestion 4. Caregivers of children who are admitted to a surgical co-management team Non-gun owners will be excluded intermittently throughout the enrollment period based on proportion of gun owners enrolled. For every 30 study participants enrolled, 10 must be gun owners. Non-gun owner enrollment will be paused until 10 gun owners are enrolled and this cycle will repeat for every 30 participants enrolled at each study site.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Guardians of hospitalized children will receive the study intervention, viewing a 3 minute educational video about the importance of secure firearm storage from the Be SMART program. Additionally, a cable gun lock will be offered to families in the intervention group along with a Frequently Asked Questions handout from Be SMART.

Group II

Active Comparator
Guardians of hospitalized children in the active comparator group will view a brief medication storage safety video produced by Safe Kids.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 2 locations

Recruiting

Children's Hospital Colorado

Aurora, United StatesOpen Children's Hospital Colorado in Google Maps
Recruiting

Monroe Carell Jr Children's Hospital at Vanderbilt

Nashville, United States
Recruiting
2 Study Centers