SAFE Spaces: Systems Aligning for Equity (SAFE) Spaces

Sponsor
New York University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05658068
Collaborator
(none)
800
1
2
37.3
21.5

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: SAFE Spaces training and coaching
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
800 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Experimental Evaluation of a Multi-site Suicide Intervention for Youth During and After Residential Placement
Actual Study Start Date :
Apr 23, 2022
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
May 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: SAFE Spaces training and coaching

Staff in facilities assigned to this arm are offered the SAFE Spaces training and coaching model.

Behavioral: SAFE Spaces training and coaching
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.

No Intervention: Training as Usual

Staff in facilities assigned to this arm receive training as usual.

Outcome Measures

Primary Outcome Measures

  1. Decreases in Suicidal Ideation Questionnaire (Davis, 1992) and suicide subscale of Massachusetts Youth Screening Instrument (Grisso et al., 2001) [1 year]

    Change in suicide ideation, thoughts, and behaviors

  2. Decreases on Self-Injurious Thoughts and Behaviors Interview (Nock et al., 2007) [1 year]

    Change in self-harm thoughts and behaviors

  3. Decreases on internalizing and externalizing subscales of Massachusetts Youth Screening Instrument (Grisso et al., 2001) [1 year]

    Change in mental health correlates of suicide

  4. Decreased burnout and increased job efficacy on the Professional Quality of Life measure (Stramm, 2016) and the Maslach Burnout Inventory [1 year]

    Change in staff burnout and job efficacy

  5. Change in responses on the Inventory of Depression and Anxiety Symptoms (Watson et al., 2007) [1 year]

    Change in staff mental health

  6. Increased suicide knowledge and response skills from Tennessee's state-wide gatekeeper training (Schut & Lockman, 2013) [1 year]

    Change in suicide knowledge and response skills

  7. Increased self-harm knowledge response skills from Tennessee's state-wide gatekeeper training (Schut & Lockman, 2013) [1 year]

    Change in self-harm knowledge and response skills

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 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

Exclusion Criteria:
  • Not placed in an ACS run-or contracted facility enrolled in the study during the study period

  • Lack of proficiency in English.

Contacts and Locations

Locations

Site City State Country Postal Code
1 New York University New York New York United States 10003

Sponsors and Collaborators

  • New York University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
New York University
ClinicalTrials.gov Identifier:
NCT05658068
Other Study ID Numbers:
  • IRB-FY2019-3228
First Posted:
Dec 20, 2022
Last Update Posted:
Dec 20, 2022
Last Verified:
Dec 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 20, 2022