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OpenTrials
Completed

NCT Number: NCT00558805

Family Intervention for Suicidal Youth: Emergency Care

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.

Completed

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Key information

Age range

10 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Los Angeles County Harbor-UCLA Medical Center, Los Angeles, California, United States

Loading trial locations.

Who can participate

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

FISP + Usual Care

Behavioral

Usual Care

Behavioral

Sponsors and collaborators

Lead sponsor

Centers for Disease Control and Prevention

Fed

Registry information

Acronym: FISP

Important dates

Study start
2003
First posted
Nov 15, 2007
Registry last updated
Nov 15, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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