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Clinical Trials/NCT06558409
NCT06558409
Recruiting
N/A

Safer Still (EP3)- An Interactive Intervention Adjunct to Traditional Care for Adolescents Who Are Discharged From Psychiatric Hospitals and Living in Households Where Firearms Are Stored Unsafely.

Jeff Bridge2 sites in 1 country80 target enrollmentNovember 7, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Suicide Prevention
Sponsor
Jeff Bridge
Enrollment
80
Locations
2
Primary Endpoint
Household Lethal Means Survey (HLMS)
Status
Recruiting
Last Updated
8 months ago

Overview

Brief Summary

The long-term goal is to decrease suicide and suicidal behaviors in at-risk youth through preventative interventions. Investigators propose to develop an interactive intervention ("Safer Still") to help promote safe storage of firearms during the critical period immediately following high-risk care transitions. The objective of this study is to develop and test the Safer Still intervention as an efficient adjunct to traditional care for adolescents aged 12-17 years who are discharged from psychiatric hospitals and living in households where firearms are stored unsafely.

Detailed Description

The objective of this study is to develop and test the Safer Still intervention as an efficient adjunct to traditional care for adolescents aged 12-17 years who are discharged from psychiatric hospitals and living in households where firearms are stored unsafely. Exploratory aims of the study are as follows: (1) Evaluate parental motivation to change firearm storage behavior as a potential mediator of the three-month intervention effect. Investigators hypothesize that higher change scores in the "action" stage of the readiness to change model1 at one month will mediate the intervention effect at three months; (2) Identify whether the response to the Safer Still intervention varies by adolescent history of suicide attempt and parental primary reason for firearm ownership at one and three months; and (3) Ascertain common parental reasons for declining to safely store firearms.

Registry
clinicaltrials.gov
Start Date
November 7, 2024
End Date
July 31, 2027
Last Updated
8 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Jeff Bridge
Responsible Party
Sponsor Investigator
Principal Investigator

Jeff Bridge

Principal Investigator: Jeffrey A Bridge, PhD,Abigail Wexner Research Institute at NCH

Nationwide Children's Hospital

Eligibility Criteria

Inclusion Criteria

  • Parent or legal guardian of an adolescent aged 12 to 17 years at time of consent
  • Have a child who is receiving psychiatric inpatient, crisis, or emergency treatment at Nationwide Children's Hospital
  • Indicate that at least one firearm is located in or around the residence of the adolescent and is stored unlocked, loaded, or both unlocked and loaded.
  • Only one parent per household is permitted to participate to avoid contamination across the two study conditions.

Exclusion Criteria

  • Inability to speak/read English
  • Lack access to a digital device (smartphone, iPad, tablet computer, desktop, laptop PC).

Outcomes

Primary Outcomes

Household Lethal Means Survey (HLMS)

Time Frame: Baseline, One month and Three months

The Household Lethal Means Survey (HLMS) asks the parent to indicate whether there are any guns kept in or around the home, and if so to describe how the gun(s) and ammunition are stored. The HLMS will be supplemented with three questions from the 2018 California Safety and Well-Being Survey. These three questions address reasons for firearm ownership, loaded handgun carrying in the past 30 days, and high-capacity magazine ownership. At follow-up, the study survey assesses whether and how firearm ownership and storage practices changed since baseline. Similar questions at baseline and follow-up are asked about lethal medications.

Secondary Outcomes

  • Stages of Change Questionnaire (SOCQ)(Baseline, One month, and Three months)

Study Sites (2)

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