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Youth-Nominated Support Team Intervention for Suicidal Adolescents

Youth Support Team Intervention for Suicidal Adolescents

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00071617
Enrollment
448
Registered
2003-10-30
Start date
2002-11-30
Completion date
2008-12-31
Last updated
2013-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicide, Attempted

Keywords

Suicide, Adolescence

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.

Interventions

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
University of Michigan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
13 Years to 17 Years
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

Design outcomes

Primary

MeasureTime frameDescription
suicidal ideation - Suicidal Ideation Questionnaire-JR3 monthType, frequency, and severity of suicidal thoughts

Secondary

MeasureTime frame
Depression - Children's Depression Rating Scale-Revised3 months

Other

MeasureTime frame
functional impairment - Child and Adolescent Functional Assessment Scale3 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026