An Evaluation of the SOS (Suicide Prevention) Program

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2012 by University of Connecticut Health Center.
Recruitment status was  Active, not recruiting
Sponsor:
Collaborators:
Substance Abuse and Mental Health Services Administration (SAMHSA)
Patterson Trust
Information provided by (Responsible Party):
ROBERT H. ASELTINE, University of Connecticut Health Center
ClinicalTrials.gov Identifier:
NCT00387855
First received: October 12, 2006
Last updated: July 23, 2012
Last verified: July 2012
  Purpose

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.


Condition Intervention
Suicide
Behavioral: SOS program

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
Official Title: An Outcome Evaluation of the SOS Suicide Prevention Program

Resource links provided by NLM:


Further study details as provided by University of Connecticut Health Center:

Primary Outcome Measures:
  • suicide attempts [ Time Frame: 3 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • knowledge about depression/suicide [ Time Frame: 3 months ] [ Designated as safety issue: No ]
  • attitudes about depression/suicide [ Time Frame: 3 months ] [ Designated as safety issue: No ]

Estimated Enrollment: 6000
Study Start Date: September 2001
Estimated Study Completion Date: December 2012
Estimated Primary Completion Date: December 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: 1
receive SOS program
Behavioral: SOS program
screening and didactic programming to raise awareness of depression suicidality
Other Name: Signs of Suicide

Detailed Description:

Three cohorts have participated in outcome evaluations of the SOS suicide prevention program to assess its effects on help-seeking, attitudes toward depression and suicide, and suicidal behavior. The first two cohorts consisted of 25 public state high schools in Massachusetts, Georgia, and Connecticut. The third cohort consisted of 9 middle schools and 10 high schools from outside of Connecticut with high proportions of military dependants.

Hypotheses:

H1: Exposure to the SOS program will be significantly associated with lower rates of suicidal ideation and suicide attempts; greater levels of help-seeking; greater knowledge of and more adaptive attitudes toward depression and suicide; and increased communication with and perceived support from peers.

H2: The reduction in suicide attempts among youths exposed to the program can be explained by increases in knowledge about depression and suicide, more favorable attitudes regarding suicide, and improved communication with and support from peers.

Methods

  1. The intervention: The SOS program was presented to students in 2 consecutive classes over a 2 day period, typically in health or social studies classes. The SOS program's teaching materials include a video and a discussion guide. The video includes dramatizations depicting the signs of suicidality and depression, recommended ways to react to someone who is depressed and suicidal, as well as interviews with real people whose lives have been touched by suicide. Students are also asked to complete the Brief Screen for Adolescent Depression (BSAD), a brief screening instrument for depression that is derived from the Diagnostic Interview Schedule for Children IV (Lucas et al., 2001).
  2. The sample: The first cohort involved approximately 4000 students in 9 high schools in Columbus Georgia, Hartford Connecticut, and western Massachusetts over a two-year period. The second cohort consisted ove an additional 1100 students were recruited from 16 Technical High Schools in Connecticut. A third cohort consisted of over 600 students from 9 middle schools and 10 high schools from outside of Connecticut with high proportions of military dependants.
  3. The research design: The experimental design for the evaluation was a randomized control group design with posttest only data collection. At the beginning of each school year approximately half of the classes of teachers presenting the program were randomly assigned to the treatment group, which received the SOS Prevention Program in the fall/winter of that year; the other half were assigned to the control group, which did not receive the program until the evaluation is completed.

To ascertain the effect of the program on participants' knowledge of and attitudes toward suicide and help seeking behavior, students in both the treatment and control groups were asked to complete a short questionnaire 3 months following implementation of the program. Questionnaires were anonymous. After the outcome evaluation was completed, the group of students who did not receive the program earlier in the school year received the complete SOS Program.

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Attendance at school participating in study
  2. English speaking youth with parental consent.

Exclusion Criteria:

1.Youth who do not speak and read English

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00387855

Locations
United States, Connecticut
UConn Health Center
Farmington, Connecticut, United States, 06030
Sponsors and Collaborators
University of Connecticut Health Center
Substance Abuse and Mental Health Services Administration (SAMHSA)
Patterson Trust
Investigators
Principal Investigator: Robert H Aseltine, PhD University of Connecticut Health Center
  More Information

Publications:
Responsible Party: ROBERT H. ASELTINE, Professor, Division of Behavioral Sciences and Community Health, University of Connecticut Health Center
ClinicalTrials.gov Identifier: NCT00387855     History of Changes
Other Study ID Numbers: CMHS1255, SM 05 014
Study First Received: October 12, 2006
Last Updated: July 23, 2012
Health Authority: United States: Institutional Review Board

Keywords provided by University of Connecticut Health Center:
suicide
depression

Additional relevant MeSH terms:
Suicide
Self-Injurious Behavior
Behavioral Symptoms

ClinicalTrials.gov processed this record on October 19, 2014