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Clinical Trials/NCT00071617
NCT00071617
Completed
Phase 2

Youth Support Team Intervention for Suicidal Adolescents

University of Michigan1 site in 1 country448 target enrollmentNovember 2002

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Suicide, Attempted
Sponsor
University of Michigan
Enrollment
448
Locations
1
Primary Endpoint
suicidal ideation - Suicidal Ideation Questionnaire-JR
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

This study will attempt to improve treatment adherence and reduce suicide risk among adolescents who are at risk for attempting suicide.

Detailed Description

Despite substantial knowledge about adolescent suicide risk factors, few studies have been conducted to identify effective interventions for suicidal adolescents. Youth-Nominated Support Team (YST) is an intervention designed to help suicidal adolescents after hospitalization. It is a psychoeducational social network intervention that targets poor treatment adherence and difficulties with social support. YST is designed to be a supplement to traditional or usual treatments. Participants are randomly assigned to receive either treatment as usual (TAU) or TAU plus YST for 3 months. Adolescents who receive TAU plus YST nominate three or four adults from their family, school, and community settings to function as support persons. The support persons participate in a psychoeducation session that focuses on the adolescent's psychiatric disorder(s), individualized treatment plan, importance of treatment adherence, and suicide risk factors. They also maintain regular contact with the adolescent to support treatment adherence and progress toward treatment goals. Adolescents have assessments at 6 weeks, 3 months, 6 months, and 12 months. Internalizing behavior problems, perceived social support, treatment adherence, adaptive functioning, severity of depression and anxiety, severity and frequency of suicidal thoughts, and suicide attempts are assessed.

Registry
clinicaltrials.gov
Start Date
November 2002
End Date
December 2008
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Cheryl A. King

Professor

University of Michigan

Eligibility Criteria

Inclusion Criteria

  • Hospitalization in a participating psychiatric facility
  • Suicidal ideation, intent, or attempt

Exclusion Criteria

  • Severe physical or cognitive impairment that makes informed consent, nominations, or participation in assessments impossible

Outcomes

Primary Outcomes

suicidal ideation - Suicidal Ideation Questionnaire-JR

Time Frame: 3 month

Type, frequency, and severity of suicidal thoughts

Secondary Outcomes

  • Depression - Children's Depression Rating Scale-Revised(3 months)

Study Sites (1)

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