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

Running, not enrolling · Not applicable

Conditions studied: Suicide, Mental Health Disorder, Anhedonia

In brief

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).

Key facts

Study ID

NCT06665620

Run by

Ksana Health

People needed

20

Starts

2025-07-16

Expected to finish

2026-02-01

Last updated by the study team

2026-01-12

Who can join

Age: 13 and older, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Recent suicide attempt or ideation with a plan
• English fluency and literacy
• Parent or legal guardian willing and able to legally provide informed consent

You may not qualify if…

• Unable to read/understand English
• Current manic or psychotic episode
• Development disability precluding comprehension of study procedures
• No routine access to a mobile phone, assessed by EHR review and during phone screen
• No eligible parent or legal guardian to provide informed consent

Where it is running

• University of Pittsburgh — Pittsburgh, Pennsylvania, United States

Full record on ClinicalTrials.gov

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