- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01603563
Stepped Care for Young Children After Trauma
April 23, 2015 updated by: University of South Florida
The aim of this R34 study is to develop and test the feasibility of a Stepped Care intervention for young children with Posttraumatic Stress Disorder (PTSD).
Phase I will focus on developing and testing the feasibility of Stepped Care Trauma-Focused Cognitive Behavioral Therapy (SC-TF-CBT) in a small open trial (N=10).
Phase II will consist of a randomized controlled trial (N=54) examining the efficacy of SC-TF-CBT relative to standard Trauma-Focused Cognitive Behavioral Therapy (TF-CBT)on a number of outcome measures, treatment acceptability and satisfaction, and costs of treatment delivery.
Findings from this pilot study will establish the feasibility and preliminary efficacy (see Kraemer et al., 2006) of SC-TF-CBT before progressing to a larger, randomized R01 to examine the effectiveness of SC-TF-CBT for early childhood PTSD.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Young children who are exposed to traumatic events such as abuse, disasters, accidents, illnesses, injury and the death of a person close to them are at risk for developing PTSD.
While effective treatments for childhood PTSD exist, novel interventions that are more accessible, efficient, and cost-effective are needed to improve access to evidence-based treatment.
The purpose of this study is to develop and test the feasibility of an intervention called Stepped Care Trauma-Focused Cognitive Behavioral Therapy which has the potential to greatly improve service delivery approaches to make treatment more accessible and less costly, thereby reducing childhood PTSD and related societal impacts and costs.
Study Type
Interventional
Enrollment (Actual)
63
Phase
- Phase 2
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Florida
-
Tampa, Florida, United States, 33613-1238
- Crisis Center of Tampa Bay
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
3 years to 7 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Child must have experienced at least one traumatic event after the age of 36 months.
- At least five Postttraumatic stress symptoms with one symptom of reexperiencing or one symptom of avoidance.
- Child must be between 3 and 7 years of age at the time of enrollment.
- The parent must be willing and able to participate in the treatment and complete informed consent.
Exclusion Criteria:
- Psychosis, mental retardation, autism, or related pervasive developmental disorders in child or any condition that would limit the caregiver's ability to understand CBT and the child's ability to follow instructions.
- Parent has had substance use disorder within the past 3 months.
- Child or parent is suicidal (the DIPA will be used to screen for child suicidal ideation and the SCID-RV will be used to screen for parent suicide ideation; assessed by all available information). A delayed entry once the parent or child is stabilized (at least 6 months post suicidal) and not having suicidal ideation will be allowed.
- Child or parent is not fluent in English.
- Child is currently taking psychotropic medication and is not on a stable medication regimen for at least 4 weeks prior to admission to the study. If appropriate, a delayed entry will be allowed so that once a child is on a stable dosage the child may be enrolled in the study.
- Child is receiving trauma-focused psychotherapy when study treatment is provided.
- Parent or caregiver who would be treatment participant was the perpetrator, or the child was perpetrated by a person who still lives in the home (e.g. mother's boyfriend, sibling).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Stepped Care TF-CBT
Patients will receive step one: 3 (1 hr.) in-office therapist-led sessions over 6 weeks, the parent-child workbook (Stepping Together), scheduled weekly phone meetings (15 minutes), and information from the National Child Traumatic Stress Network website (via web or paper for those without access).
Children who do not meet responder status will receive step two: 9 (1 to 1.5 hr.) in-office therapist-directed sessions of TF-CBT over 6 to 8 weeks.
|
Stepped Care TF-CBT patients will receive step one: 3 (1 hr.) in-office therapist-led sessions over 6 weeks, the parent-child workbook (Stepping Together), scheduled weekly phone meetings (15 minutes), and information from the National Child Traumatic Stress Network website (via web or paper for those without access).
Children who do not meet responder status will receive step two: 9 (1 to 1.5 hr.) in-office therapist-directed sessions of TF-CBT over 6 to 8 weeks.
|
|
Active Comparator: Standard TF-CBT
Patients will receive 12 (1 to 1.5 hr.) standard weekly in-office therapist-directed sessions over 12 to 14 weeks (Phase II only).
The 2 additional weeks allow for scheduling difficulty.
Standard TF-CBT includes child, parent and conjoint parent-child sessions addressing the core trauma treatment components discussed in section a.3 (e.g.
stress management, skill building, gradual exposure, & trauma narrative etc.).
|
Standard TF-CBT patients will receive 12 (1 to 1.5 hr.) standard weekly in-office therapist-directed sessions over 12 to 14 weeks (Phase II only).
The 2 additional weeks allow for scheduling difficulty.
Standard TF-CBT includes child, parent and conjoint parent-child sessions addressing the core trauma treatment components discussed in section a.3 (e.g.
stress management, skill building, gradual exposure, & trauma narrative etc.).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Posttraumatic stress symptoms
Time Frame: baseline, week 14, and 3 month follow up
|
Change from baseline in Diagnostic Preschool Infant Assessment PTSD module (DIPA; Scheeringa, 2010) and in the Trauma Symptom Checklist for Young Children (Briere et al., 2001) at 14 weeks and 3 month follow up
|
baseline, week 14, and 3 month follow up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Externalizing behaviors
Time Frame: baseline and week 14 and 3 month follow up
|
Change from baseline in the Child Behavior Checklist (Achenbach & Rescorla, 2000) externalizing behaviors at 14 weeks and 3 month follow up
|
baseline and week 14 and 3 month follow up
|
|
Internalizing behaviors
Time Frame: baseline, week 14 and 3 month follow up
|
Change from baseline in the Child Behavior Checklist (Achenbach & Rescorla, 2000) internalizing behaviors at week 14 and 3 month follow up
|
baseline, week 14 and 3 month follow up
|
|
Independent Evaluator-rated PTSD symptom and impairment severity
Time Frame: baseline, week 14 and 3 month follow up
|
Change from baseline in clinical global impression severity (NIMH, 1985)at week 14 and 3 month follow up
|
baseline, week 14 and 3 month follow up
|
|
Global improvement
Time Frame: baseline, week 14 and 3 month follow up
|
Change from baseline in clinical global impression - improvement (Guy, 1976)at week 14 and 3 month follow up
|
baseline, week 14 and 3 month follow up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Alison A Salloum, PhD, University Of South Florida
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2011
Primary Completion (Actual)
August 1, 2014
Study Completion (Actual)
November 1, 2014
Study Registration Dates
First Submitted
May 9, 2012
First Submitted That Met QC Criteria
May 18, 2012
First Posted (Estimate)
May 23, 2012
Study Record Updates
Last Update Posted (Estimate)
April 24, 2015
Last Update Submitted That Met QC Criteria
April 23, 2015
Last Verified
April 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1R34MH092373-01A1 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Posttraumatic Stress Disorder
-
Sofie FolkeAarhus University Hospital; Copenhagen Trial Unit, Center for Clinical Intervention... and other collaboratorsNot yet recruiting
-
University Hospital, ToursCompletedPostTraumatic Stress DisorderFrance
-
ARQ National Psychotrauma CentreLeiden University Medical CenterEnrolling by invitationPosttraumatic Stress Disorder (PTSD)Netherlands
-
The University of Texas Health Science Center at...University of Pennsylvania; Brooke Army Medical Center; C.R.Darnall Army Medical... and other collaboratorsCompletedPosttraumatic Stress Disorder (PTSD)United States
-
Icahn School of Medicine at Mount SinaiCompletedPosttraumatic Stress Disorder (PTSD)United States
-
Berlin Center for the Treatment of Torture VictimsCompletedPosttraumatic Stress Disorder (PTSD)Germany
-
VA Office of Research and DevelopmentCompletedPosttraumatic Stress Disorder (PTSD)United States
-
Michael E. DeBakey VA Medical CenterSouth Central VA Mental Illness Research, Education & Clinical CenterCompletedPosttraumatic Stress Disorder (PTSD)United States
-
TEMPVA Research Group, Inc.C.R.Darnall Army Medical Center; VA Boston Healthcare System; Central Texas Veterans...UnknownPosttraumatic Stress Disorder, Combat-relatedUnited States
-
VA Office of Research and DevelopmentCompleted
Clinical Trials on Stepped Care TF-CBT
-
University of South FloridaCompletedPosttraumatic Stress DisorderUnited States
-
Norwegian Center for Violence and Traumatic Stress...University of South FloridaCompletedDepressive Symptoms | Parental Stress | Post Traumatic Stress Disorder (PTSD) | Health Related Quality of LifeNorway
-
Hartford HospitalNational Institute of Mental Health (NIMH)Completed
-
Baylor College of MedicineCompletedObsessive-Compulsive Disorder | Anxiety Disorders | Generalized Anxiety Disorder | Autism Spectrum Disorder | Social Anxiety Disorder | Specific Phobia | Cognitive Behavioral TherapyUnited States
-
Dr. Nazanin AlaviCompletedDepression | Depressive Symptoms | Major Depressive DisorderCanada
-
Milton S. Hershey Medical CenterEunice Kennedy Shriver National Institute of Child Health and Human Development...CompletedChild Abuse | Posttraumatic StressUnited States
-
University of WashingtonNational Institute of Mental Health (NIMH)RecruitingTrauma and Stressor Related Disorders | Trauma, PsychologicalUnited States
-
The University of Hong KongThe Hong Kong Jockey Club Charities Trust; Baptist Oi Kwan Social Service; Hong... and other collaboratorsRecruiting
-
Medical University of South CarolinaCompletedPost Traumatic Stress DisorderUnited States
-
Universidad Complutense de MadridMinistry of Science and Innovation, Spain; Spanish Association of Victims of...CompletedAnxiety Disorders | Major Depressive Disorder | Posttraumatic Stress Disorder