Youth-Nominated Support Team Intervention for Suicidal Adolescents
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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 2 |
| 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 |
| Estimated Enrollment: | 532 |
| Study Start Date: | November 2002 |
| Study Completion Date: | December 2006 |
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 |
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| United States, Michigan | |
| Child and Adolescent Psychiatry Hospital, University of Michigan | |
| Ann Arbor, Michigan, United States, 48109 | |
| 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 May 23, 2013