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An Evaluation of the SOS (Suicide Prevention) Program

NCT00387855 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 6471

Last updated 2016-07-29

No results posted yet for this study

Summary

The purpose of this study was to investigate the impact of the SOS suicide prevention program on help-seeking, attitudes toward depression and suicide, and suicidal behavior among high school students. Current research protocol has extended this evaluation to the Middle School version of SOS.

Conditions

  • Suicide

Interventions

BEHAVIORAL

SOS program

screening and didactic programming to raise awareness of depression suicidality

Sponsors & Collaborators

  • Substance Abuse and Mental Health Services Administration (SAMHSA)

    collaborator FED

  • Patterson Trust

    collaborator UNKNOWN

  • United States Department of Defense

    collaborator FED

  • UConn Health

    lead OTHER

Principal Investigators

  • Robert H Aseltine, PhD · UConn Health

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-09-30
Primary Completion
2012-12-31
Completion
2014-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00387855 on ClinicalTrials.gov