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.
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Notify MeKey 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
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
Usual Care
BehavioralSponsors 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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