Systems Aligning for Equity (SAFE) Spaces
SAFE Spaces
Experimental Evaluation of a Multi-site Suicide Intervention for Youth During and After Residential Placement
1 other identifier
interventional
1,000
1 country
1
Brief Summary
The goal of this 2-arm cluster randomized clinical trial is to test whether an evidence-based staff training and coaching model specifically designed as a response to legal system-involved youths' and frontline staff's mental health needs can improve the safety and suicide outcomes, mental health challenges, and wellness and facility climate for youth and staff in facilities assigned to the intervention condition. Staff in facilities assigned to the intervention are eligible to receive evidence-based programming in suicide detection and prevention (Shield of Care; SOC) and wellness skill-building (Skills for Life) through training and personalized coaching. Multiple training sessions will be offered to small groups of staff in-person in residential facilities and paired with personalized in-person and virtual coaching. Staff and youth in all facilities will be asked to complete periodic surveys assessing experiences in the facility, suicide and safety knowledge and risk, and their mental health and wellness. Researchers will compare outcomes of staff in youth in facilities assigned to the intervention compared to facilities in the training-as-usual condition.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Apr 2022
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 23, 2022
CompletedFirst Submitted
Initial submission to the registry
December 1, 2022
CompletedFirst Posted
Study publicly available on registry
December 20, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2025
CompletedJanuary 7, 2026
July 1, 2025
3.2 years
December 1, 2022
January 5, 2026
Conditions
Outcome Measures
Primary Outcomes (7)
Decreases in Suicidal Ideation Questionnaire (Davis, 1992) and suicide subscale of Massachusetts Youth Screening Instrument (Grisso et al., 2001)
Change in suicide ideation, thoughts, and behaviors
1 year
Decreases on Self-Injurious Thoughts and Behaviors Interview (Nock et al., 2007)
Change in self-harm thoughts and behaviors
1 year
Decreases on internalizing and externalizing subscales of Massachusetts Youth Screening Instrument (Grisso et al., 2001)
Change in mental health correlates of suicide
1 year
Decreased burnout and increased job efficacy on the Professional Quality of Life measure (Stramm, 2016) and the Maslach Burnout Inventory
Change in staff burnout and job efficacy
1 year
Change in responses on the Inventory of Depression and Anxiety Symptoms (Watson et al., 2007)
Change in staff mental health
1 year
Increased suicide knowledge and response skills from Tennessee's state-wide gatekeeper training (Schut & Lockman, 2013)
Change in suicide knowledge and response skills
1 year
Increased self-harm knowledge response skills from Tennessee's state-wide gatekeeper training (Schut & Lockman, 2013)
Change in self-harm knowledge and response skills
1 year
Study Arms (2)
SAFE Spaces training and coaching
EXPERIMENTALStaff in facilities assigned to this arm are offered the SAFE Spaces training and coaching model.
Training as Usual
NO INTERVENTIONStaff in facilities assigned to this arm receive training as usual.
Interventions
Staff in facilities assigned to the intervention are eligible to receive evidence-based programming in suicide detection and prevention (Shield of Care; SOC) and wellness skill-building (Skills for Life) through training and personalized coaching. Multiple training sessions will be offered to small groups of staff in-person in residential facilities and paired with personalized in-person and virtual coaching.
Eligibility Criteria
You may qualify if:
- Placement in in ACS-run or contracted residential facilities enrolled in the study during the first 2 years of the intervention period
- Proficiency in English
You may not qualify if:
- Not placed in an ACS run-or contracted facility enrolled in the study during the study period
- Lack of proficiency in English.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
New York University
New York, New York, 10003, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 1, 2022
First Posted
December 20, 2022
Study Start
April 23, 2022
Primary Completion
June 30, 2025
Study Completion
June 30, 2025
Last Updated
January 7, 2026
Record last verified: 2025-07