RECRUITING

SAFETY-A for Promoting Equity in Suicide Prevention Outcomes in Schools

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study will adapt Safe Alternatives For Teens and Youth - Acute (SAFETY-A) for implementation in low-resourced school districts to reduce racial/ethnic disparities in mental health service use (MHS) following identification of suicide risk in youth. SAFETY-A will be adapted to fit the organizational context of school districts and to reduce mistrust of MHS, internalized stigma, and concealment of youth emotional distress that arise in school suicide risk assessments with Asian American and Latinx students. Following a prototyping case series, a feasibility trial will assign four districts to the timing of SAFETY-A implementation to generate preliminary data on feasibility and impacts on proposed mechanisms and youth MHS utilization and clinical outcomes across racial/ethnic groups.

Official Title

SAFETY-A for Promoting Equity in Suicide Prevention Outcomes in Schools

Quick Facts

Study Start:2022-11-01
Study Completion:2025-02
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05834660

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:11 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age 11-19
  2. 2. Enrolled in participating school district
  3. 3. Present with suicide thoughts or behavior to school personnel
  4. 4. Have an identified caregiver who can participate in the intervention
  1. 1. School personnel determine the student to be at such imminent risk of danger to self that they are unable to benefit from the intervention and must be immediate transported for emergency care.
  2. 2. Student is unable to participate in the intervention due to indications of intellectual disability, psychosis, or intoxication

Contacts and Locations

Study Contact

Anna S Lau, PhD
CONTACT
310-206-5363
alau@psych.ucla.edu
Ashley Flores
CONTACT
aflores@psych.ucla.edu

Principal Investigator

Anna S Lau, PhD
PRINCIPAL_INVESTIGATOR
University of California, Los Angeles

Study Locations (Sites)

University of California Los Angeles
Los Angeles, California, 90095
United States

Collaborators and Investigators

Sponsor: University of California, Los Angeles

  • Anna S Lau, PhD, PRINCIPAL_INVESTIGATOR, University of California, Los Angeles

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-11-01
Study Completion Date2025-02

Study Record Updates

Study Start Date2022-11-01
Study Completion Date2025-02

Terms related to this study

Keywords Provided by Researchers

  • Implementation Feasibility
  • Implementation Acceptability

Additional Relevant MeSH Terms

  • Suicidal Ideation