Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
An Evaluation of the SOS Program
This study is currently recruiting participants.
Verified by University of Connecticut, September 2008
Sponsors and Collaborators: University of Connecticut Health Center
Substance Abuse and Mental Health Services Administration (SAMHSA)
Patterson Trust
Information provided by: University of Connecticut
ClinicalTrials.gov Identifier: NCT00387855
  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.


Condition Intervention
Suicide
Behavioral: SOS program

MedlinePlus related topics: Depression Suicide
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Parallel Assignment, Efficacy Study
Official Title: An Outcome Evaluation of the SOS Suicide Prevention Program

Further study details as provided by University of Connecticut:

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: May 2009
Estimated Primary Completion Date: May 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
receive SOS program
Behavioral: SOS program
screening and didactic programming to raise awareness of depression suicidality

Detailed Description:

Nine high schools in Massachusetts, Georgia, and Connecticut participated in an outcome evaluation of the SOS suicide prevention program to assess its effects on help-seeking, attitudes toward depression and suicide, and suicidal behavior.

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 study involved approximately 4000 students in 9 high schools in Columbus Georgia, Hartford Connecticut, and western Massachusetts over a two-year period.
  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:

  • attended schools participating in study
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00387855

Contacts
Contact: Amy James, PhD 860 679-2021 ajames@uchc.edu

Locations
United States, Connecticut
UConn Health Center Recruiting
Farmington, Connecticut, United States, 06030
Contact: Amy James     860-679-2021        
Principal Investigator: Robert H Aseltine, PhD            
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: University of Connecticut Health Center ( Robert Aseltine PhD, Associate Professor )
Study ID Numbers: CMHS1255, SM 05 014
Study First Received: October 12, 2006
Last Updated: September 7, 2008
ClinicalTrials.gov Identifier: NCT00387855  
Health Authority: United States: Institutional Review Board

Keywords provided by University of Connecticut:
suicide
depression

Study placed in the following topic categories:
Depression
Suicide
Depressive Disorder
Behavioral Symptoms
Self-Injurious Behavior

ClinicalTrials.gov processed this record on January 16, 2009