Optimal Treatment Strategies for Sexually Abused Children

NCT00073684 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 210

Last updated 2014-05-08

No results posted yet for this study

Summary

This study will determine the necessity of including abuse-focused interventions in the treatment of sexually abused children.

Conditions

  • Child Abuse, Sexual

Interventions

BEHAVIORAL

Trauma focused cognitive behavioral therapy (TF-CBT)

This study aims to: (1) examine the differential effects of CBT with and without trauma narrative interventions; (2) examine the comparative efficacy of brief and extended (8 vs. 16 sessions) individual CBT; (3) make developmental comparisons between 4-7 year olds and 8-11 year olds as to the appropriateness and therapeutic necessity of exposure interventions and longer treatment; and (4) identify child and parent factors that may significantly mediate the relationships between treatment conditions and outcomes. The findings of this study will help establish clinical as well as developmental markers for the early identification of sexually abused children who may require more focused (i.e., including trauma narrative) and/or longer treatment to achieve optimal outcomes.

BEHAVIORAL

Brief abuse-focused treatment

Participants will receive 8 sessions of TF-CBT with abuse-focused treatment.

BEHAVIORAL

Brief coping skills treatment

Participants will receive 8 sessions of TF-CBT with brief coping skills treatment.

BEHAVIORAL

Extended abuse-focused treatment

Participants will receive 16 sessions of TF-CBT with extended abuse-focused treatment.

BEHAVIORAL

Extended coping skills treatment

Participants will receive 16 sessions of TF-CBT with extended coping skills treatment.

Sponsors & Collaborators

  • National Institute of Mental Health (NIMH)

    collaborator NIH
  • Rowan University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
4 Years
Max Age
11 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-08-31
Primary Completion
2009-07-31
Completion
2009-07-31

Countries

  • United States

Study Locations

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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 NCT00073684 on ClinicalTrials.gov