RECRUITING

Safer Storage Safer Homes An Inpatient Pediatric Lethal Means Counseling Pilot Trial

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Firearm injuries are the leading cause of death for American youth. Strikingly, firearm suicide among adolescents is growing faster than other groups. Lethal means counseling is standard of care, however, infrequently occurs despite pediatricians recognizing the importance. Lack of time, topic discomfort, and inadequate resources for families are commonly reported barriers to counseling. By addressing these factors, we can improve counseling with the ultimate goal of increasing safe storage and reducing firearm injuries in youth. Children admitted in acute mental health crises while awaiting psychiatric hospital placement are a population at greater risk of suicide. We plan to implement a pilot intervention to offer secure storage counseling and storage device distribution to families of behavioral health patients who indicate firearm ownership on initial screening. The goal of this project is to evaluate the feasibility and acceptability of firearm secure storage counseling and device provision in the inpatient setting.

Official Title

Safer Storage Safer Homes: Investigating the Use of Secure Storage Devices in the Inpatient Behavioral Health Population

Quick Facts

Study Start:2025-07-08
Study Completion:2026-04
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06479889

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Guardian of child ages 0-18 years old who is admitted to and receiving care on the MCJCHV Behavioral Health Team
  2. 2. Guardian age \> or = 18 years
  3. 3. Guardian with phone access to receive calls or email access to receive study information electronically
  4. 4. English or Spanish-speaking guardian
  5. 5. Guardian self-identifies as firearm owner
  1. 1. Guardian of children outside the specified age range
  2. 2. Guardian speaks a language that is not English or Spanish
  3. 3. Lack of telephone or email contact
  4. 4. Guardian age is outside of the specific age range
  5. 5. Guardians/children who do not otherwise meet the eligibility criteria listed in section above as determined by pre-screen
  6. 6. Guardian or child in distress at time of enrollment

Contacts and Locations

Study Contact

justine.c.stassun@vumc.org Gastineau, MD MPH
CONTACT
615-936-7276
kelsey.gastineau@vumc.org
Justine Stassun, MS
CONTACT
justine.c.stassun@vumc.org

Principal Investigator

Kelsey Gastineau
PRINCIPAL_INVESTIGATOR
Vanderbilt University Medical Center

Study Locations (Sites)

Monroe Carell Jr Children's Hospital at Vanderbilt
Nashville, Tennessee, 37232
United States

Collaborators and Investigators

Sponsor: Vanderbilt University Medical Center

  • Kelsey Gastineau, PRINCIPAL_INVESTIGATOR, Vanderbilt University Medical Center

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 Registration Dates

Study Start Date2025-07-08
Study Completion Date2026-04

Study Record Updates

Study Start Date2025-07-08
Study Completion Date2026-04

Terms related to this study

Additional Relevant MeSH Terms

  • Firearm Injury
  • Hospitalizations Psychiatric