Clinical Trial

Optimizing a Just-in-time Adaptive Intervention for Suicide Safety Planning in Adolescents

Completed
View on ClinicalTrials.gov →
Summary
Despite efforts to prevent suicide, US rates are climbing, and suicide is the second leading cause of death amongst youth. Digital tools, especially personal smartphones, are promising avenues to address these issues and can be used to increase engagement with effective interventions such as suicide safety planning. The BRITE suicide safety planning app was developed on evidence-based principles and has undergone rigorous formative development and effectiveness evaluations. However, to optimize its functionality, commercial viability, and scale its implementation, issues related to user engagement need to be addressed. This 4-week Micro-Randomized Trial (MRT) will optimize specific components of ViraBrite, an augmented version of the BRITE suicide safety planning app that integrates automated algorithms (i.e., just in time adaptive intervention features) to facilitate increased engagement with coping skills and pushes safety planning materials to users at periods of high risk (i.e., increases in emotional distress).
Protocol Amendment History 2 changes
critical Trial completed 2026-08-13
notable Enrollment increased: 20 -> 24 participants 2026-08-13
Trial Details
NCT Number NCT06665620
Lead Sponsor Ksana Health
Collaborators: University of Pittsburgh Medical Center, National Institute of Mental Health (NIMH)
Conditions Suicide, Mental Health Disorder, Anhedonia
Enrollment 24 participants
Start Date 2025-07-16
Primary Completion 2026-02-01 (estimated)
Study Completion 2026-02-01 (estimated)
Updated on ClinicalTrials.gov 2026-08-12