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Youth-Nominated Support Team Intervention for Suicidal Adolescents
This study has been completed.

First Received on October 29, 2003.   Last Updated on December 10, 2007   History of Changes
Sponsor: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier: NCT00071617
  Purpose

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


Condition Intervention Phase
Suicide, Attempted
Behavioral: Youth-Nominated Support Team
Phase II

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Youth Support Team Intervention for Suicidal Adolescents

Resource links provided by NLM:


Further study details as provided by National Institute of Mental Health (NIMH):

Estimated Enrollment: 532
Study Start Date: November 2002
Study Completion Date: December 2006
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.

  Eligibility

Ages Eligible for Study:   13 Years to 17 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00071617

Locations
United States, Michigan
Child and Adolescent Psychiatry Hospital, University of Michigan
Ann Arbor, Michigan, United States, 48109
Sponsors and Collaborators
Investigators
Principal Investigator: Cheryl A. King, Ph.D. University of Michigan
  More Information

Additional Information:
No publications provided

ClinicalTrials.gov Identifier: NCT00071617     History of Changes
Other Study ID Numbers: R01 MH63881, DSIR 84-CTS
Study First Received: October 29, 2003
Last Updated: December 10, 2007
Health Authority: United States: Federal Government

Keywords provided by National Institute of Mental Health (NIMH):
Suicide
Adolescence

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

ClinicalTrials.gov processed this record on February 12, 2012