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Evaluation of the Child and Family Traumatic Stress Intervention

NCT01031615 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 112

Last updated 2011-06-16

No results posted yet for this study

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.

Conditions

Interventions

BEHAVIORAL

Child and Family Traumatic Stress Interv (CFTSI)

4 sessions involving both the target child and a parent/caregiver

BEHAVIORAL

Psychoeducational Comparison

4 individually focused sessions including psychoeducation and relaxation.

Sponsors & Collaborators

  • Yale University

    lead OTHER

Principal Investigators

  • Steven Berkowitz, M.D. · University of Pennsylvania

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
7 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-10-31
Primary Completion
2009-09-30
Completion
2009-09-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01031615 on ClinicalTrials.gov