Swift Outpatient Alternatives for Rapid Stabilization — SOARS  

Suicidal Ideation Clinical Trial

Official title: Swift Outpatient Alternatives for Rapid Stabilization

Status Recruiting

Clinical Trial Summary

The goal of this clinical trial is to improve the effective outpatient management of acute youth suicide risk by optimizing intervention components to build an efficient, evidence-based intervention that is responsive to the needs of, and coordinated with, providers in primary care settings. The main questions are:

1. What is the strongest combination of SOARS components associated with reduction in youth suicidal thoughts and behavior (STB)?

2. Do age and STB history moderate the impact of the effects of the SOARS intervention components?

3. Do therapeutic alliance, youth and caregiver self-efficacy account for changes in youth STBs?

4. What helps medical outpatient providers refer to SOARS and continue care after SOARS?

Clinical Trial Description

The investigators are comparing different treatment sequences for suicidal thoughts and behaviors. The treatment package families are assigned will be determined by randomization.

All participants will receive 1 session of Collaborative Assessment and Management of Suicidality (CAMS) and care management. CAMS treatment primarily focuses on working with a therapist to understand the reasons why the participants are thinking about suicide Additional components which the participant may be randomly assigned to receive include coping skills training for youth, skills training for parents, and additional safety strategies. Each treatment type is designed to help adolescents and young adults with suicide risk.

Participants will be randomly assigned to an intervention sequence for a minimum of 1 session (120 minutes) and maximum of 8 sessions (440 minutes, divided across separate youth and caregiver components).

Caregivers will receive at least 1 session and a maximum of 4 sessions. Depending on the randomization, caregivers may be assigned to receive skills related to caregiving and safe storage of items that could be used for harm.

To see how the treatment is going participants will receive study assessments at the beginning of the study, 1-month, and 2-months. Study assessments will ask about demographics, suicide attempts, suicidal ideation, non-suicidal self-injury, experiences with treatment, substance use, and social experiences. The research team will also collect information from medical records. ;

Related Conditions & MeSH terms

• Suicidal Ideation
• Suicide
• Suicide Attempt
• Suicide, Attempted

• NCT number: NCT05996172
• Study type: Interventional
• Source: University of Washington
• Contact: Molly Adrian
• Phone: 206-987-7183
• Email: molly.adrian@seattlechildrens.org
• Status: Recruiting
• Phase: N/A
• Start date: November 9, 2023
• Completion date: January 2028