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Clinical Trials/NCT01031615
NCT01031615
Completed
Phase 1

Evaluation of the Child and Family Traumatic Stress Intervention

Yale University1 site in 1 country112 target enrollmentOctober 2005
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ConditionsPosttraumatic Stress Disorder

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Posttraumatic Stress Disorder
Sponsor
Yale University
Enrollment
112
Locations
1
Primary Endpoint
UCLA Posttraumatic Reaction Index (PTSD-RI)
Status
Completed
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this study is to determine the efficacy of the Child and Family Traumatic Stress Intervention (CFTSI) in preventing the development of Posttraumatic Stress Disorder (PTSD) when implemented within 30 days of a potentially traumatic event.

Registry
clinicaltrials.gov
Start Date
October 2005
End Date
September 2009
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Youth exposed to a potentially traumatic event within the last 30 days who have one new symptom on the Posttraumatic Checklist (PCL)

Exclusion Criteria

  • •Already receiving mental health treatment
  • •Autism or Developmental Disability
  • •Diagnosed with psychosis or bipolar disorder
  • •Non-english speaking

Outcomes

Primary Outcomes

UCLA Posttraumatic Reaction Index (PTSD-RI)

Time Frame: 3 months post-intervention

Secondary Outcomes

  • Trauma Symptom Checklist for Children (TSCC)(3 Months post-intervention)

Study Sites (1)

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