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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00558805
Other study ID # 921708
Secondary ID
Status Completed
Phase Phase 2
First received November 14, 2007
Last updated November 14, 2007
Start date October 2003

Study information

Verified date October 2007
Source Centers for Disease Control and Prevention
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

This project evaluates a brief intervention in the emergency department (ED) for adolescents presenting with suicide attempts. The intervention aims to capitalize on the opportunity offered by the ED visit to deliver an effective intervention, improve adherence to follow-up care, decrease the risk of repeat suicide attempts, and improve clinical and functioning outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 10 Years to 18 Years
Eligibility Inclusion Criteria:

- 10-18 years

- Suicidal patient presenting to Emergency Department

Exclusion Criteria:

- Acute psychosis/symptoms that impede consent/assessment

- No parent/guardian to consent (youth <18)

- Youth not English-speaking

- Parents/guardians not English or Spanish-speaking.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
FISP + Usual Care

Usual Care


Locations

Country Name City State
United States Los Angeles County Harbor-UCLA Medical Center Los Angeles California
United States UCLA Emergency Medical Center Los Angeles California

Sponsors (1)

Lead Sponsor Collaborator
Centers for Disease Control and Prevention

Country where clinical trial is conducted

United States, 

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