Clinical Trial

Lock and Protect: Reducing Adolescent Access to Lethal Means of Suicide

Enrolling by Invitation
View on ClinicalTrials.gov →
Summary
The primary goal is to determine the acceptability and feasibility of implementing the Lock and Protect decision aid. The secondary goals are to identify the potential short-term impact of Lock and Protect on home firearm and medication storage, parental self-efficacy. Using interviews with caregivers, the study will clarify the acceptability, feasibility, and barriers to implementing the Lock and Protect hone safety plan. This will allow further development of effective strategies to subsequently further test and use Lock and Protect in the ED. NOTE: The study will only recruit guardians and their adolescents from the pediatric ED at Morgan Stanley Children's Hospital NY-Presbyterian.
Protocol Amendment History 4 amendments
This ClinicalTrials.gov record has been amended 4 times since 2025-08-06; most recent amendment 2025-12-01.
Status change: Recruiting → Enrolling by Invitation 2025-12-01
Status change: Not Yet Recruiting → Recruiting 2025-10-21
Trial Details
NCT Number NCT07111052
Lead Sponsor Columbia University
Conditions Suicide, Suicide Attempt, Adolescent Suicidality, Suicide Ideation
Enrollment 50 participants
Start Date 2025-09-11
Primary Completion 2026-12-31 (estimated)
Study Completion 2027-03 (estimated)
Updated on ClinicalTrials.gov 2025-12-05