Skip to main content
Clinical Trials/NCT01649141
NCT01649141
Unknown
N/A

National Child Traumatic Stress Initiative: Community Treatment and Service Centers

Delaware Division of Prevention and Behavioral Health Services1 site in 1 country110 target enrollmentAugust 2006

Overview

Phase
N/A
Intervention
Not specified
Conditions
Posttraumatic Stress Disorder
Sponsor
Delaware Division of Prevention and Behavioral Health Services
Enrollment
110
Locations
1
Primary Endpoint
Change in baseline PTSD Symptoms at 3-,6-,9- and 12-months
Last Updated
13 years ago

Overview

Brief Summary

This effectiveness study is being conducted to determine whether Trauma-Focused Cognitive Therapy (TF-CBT), a treatment model developed in specialty clinics by experts in the treatment of child sexual abuse, can be effectively transported to a state-contracted community mental health agency in the state of Delaware and used effectively by clinicians with little prior TF-CBT experience. The sample is comprised of youths receiving public mental health services and with diverse trauma histories.

Detailed Description

This investigation aims to examine the effectiveness of Trauma-Focused Cognitive Behavioral Therapy (TF-CBT) in treating child traumatic stress when implemented in community settings on a state-wide level in Delaware. Youth (ages 7-16 years) with a history of documented trauma (sexual or physical abuse, traumatic loss, domestic or community violence) and symptoms of Posttraumatic Stress Disorder (PTSD) receive approximately 10 sessions of TF-CBT delivered in a state-contracted mental health agency. Children and adolescents are recruited from a public mental health population. PTSD symptoms and internalizing and externalizing behavior problems have been assessed in the first 72 participants at pre-treatment and then at 3-, 6-, 9-, and 12-months after intake; subsequent participants (n=38) are only being assessed for symptoms and problems at pre-treatment and then at 3-, 6-months after intake.

Registry
clinicaltrials.gov
Start Date
August 2006
End Date
December 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Delaware Division of Prevention and Behavioral Health Services
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • child is 7-17 years old
  • positive screen for PTSD
  • child qualifies for public insurance
  • parent willing to co-participate in treatment
  • English-speaking (child and parent)

Exclusion Criteria

  • intellectual disability (child)
  • untreated psychosis (child)
  • untreated substance abuse (child)
  • sibling already in study
  • unable to participate in year-long follow-up (e.g., moving out of state)

Outcomes

Primary Outcomes

Change in baseline PTSD Symptoms at 3-,6-,9- and 12-months

Time Frame: Baseline and post-baseline (3-,6-,9-,12-months)

PTSD symptoms area assessed with the UCLA PTSD Reaction Index for DSM-IV (UPID). The UPID (Pynoos, et al., 1998) includes 48 items that can be administered as a questionnaire or structured interview. The instrument's three sections assess for trauma exposure and symptoms of DSM-IV PTSD in children ages 7-18. The UPID has good convergent validity (i.e., 0.70 in comparison to the K-SADS, epidemiologic version), a sensitivity of 0.93 and specificity of 0.87 in diagnosing PTSD (Steinberg et al., 2004), and test-retest reliability of 0.84 (Steinberg et al., 2004)

Secondary Outcomes

  • Change in baseline behavioral problems at 3-, 6-, 9- and 12-months.(Baseline and post-baseline (3-,6-,9-,12-months))

Study Sites (1)

Loading locations...

Similar Trials