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Using Neuroimaging to Understand Children's Mental Health and Treatment Outcomes

Primary Purpose

Anxiety, Depression, Trauma

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Modular Approach to Therapy for Children with Anxiety, Depression, Trauma, and Conduct Problems
Monitoring and Feedback System
Treatment as usual
Sponsored by
Harvard University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety focused on measuring anxiety, depression, trauma, behavior problems, evidence-based treatments, manualized treatments, cognitive-behavioral therapy, youth, mental health, self-regulation, neuroimaging

Eligibility Criteria

7 Years - 13 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. enrolled in grades 3-7
  2. have a primary clinical problem in the areas of anxiety, depression, conduct, or posttraumatic stress
  3. clinically elevated problem levels on the Internalizing, Externalizing, Anxious-Depressed, Withdrawn-Depressed, Aggressive Behavior, or Rule-Breaking Behavior scales of the Child Behavior Checklist or Youth Self-Report or on the UCLA Post-Traumatic Stress Disorder Reaction Index.

Exclusion Criteria:

  1. Mental retardation
  2. Pervasive developmental disorder
  3. Eating disorder
  4. children for whom attention problems or hyperactivity are the primary referral concern
  5. active psychosis and/or a suicide attempt in the previous year

To participate in the two neuroimaging tasks (Emotion Regulation Task; Emotional Go/No Go Task), participants must be healthy (no major medical illness), right-handed, fluent in English, have no history of neurological impairment (including but not limited to history of loss of consciousness for great than 20 minutes, seizures, stroke, etc.), have normal or corrected to normal vision, and have no contra-indications or risk factors for MRI research (such as braces or metal implants).

Sites / Locations

  • Harvard University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Child STEPS

Usual Care

Arm Description

Child STEPs includes (1) a treatment protocol, Modular Approach to Therapy for Children with Anxiety, Depression, Trauma or Conduct Problems (MATCH-ADTC), and (2) a youth monitoring and feedback system (MFS).

Treatment in the UC condition will use the procedures therapists and their supervisors consider appropriate and believe to be effective, and researchers will not influence their work.

Outcomes

Primary Outcome Measures

Change from Baseline Emotion Regulation Task at End of Treatment
Change from Baseline Emotional Go/No-Go Task at End of Treatment

Secondary Outcome Measures

Change from Baseline Attentional Bias Task at End of Treatment
Change from Baseline Granularity Task at End of Treatment
Change from Baseline Behavior Rating Inventory of Executive Function (BRIEF) at End of Treatment
Change from Baseline Early Adolescent Temperament Questionnaire Revised (EATQ-R) at End of Treatment

Full Information

First Posted
March 28, 2017
Last Updated
March 8, 2021
Sponsor
Harvard University
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1. Study Identification

Unique Protocol Identification Number
NCT03112265
Brief Title
Using Neuroimaging to Understand Children's Mental Health and Treatment Outcomes
Official Title
Using Neuroimaging to Understand Children's Mental Health and Treatment Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
July 31, 2020 (Actual)
Study Completion Date
July 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Harvard University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The study will compare the impact of Child STEPs versus usual school-based therapy on neural and companion behavioral measures of self-regulation.
Detailed Description
This project will implement and evaluate the Child STEPs treatment approach as compared to "treatment as usual" (known as Usual Care or UC) through a randomized controlled trial (RCT) at eight K-8 public schools. The STEPs model has two components: (1) a modular protocol that combines 33 modules-i.e., descriptions of common elements within evidence-based therapies for anxiety, depression, post-traumatic stress, and conduct problems; and (2) a web-based system for monitoring student responses to treatment and providing weekly feedback to therapists to guide their selection and sequencing of the STEPs modules. The project will examine: (a) whether self-regulation skills at baseline are associated with baseline patterns of mental health and school problems; (b) whether self-regulation skills at baseline predict degree of improvement during treatment; (c) whether self-regulation skills improve from pre-to post treatment, and whether extent of this improvement differs by treatment condition; and (d) whether self-regulation improvement (from pre-to-post treatment) mediates the long-term benefit of treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety, Depression, Trauma, Behavior Problems
Keywords
anxiety, depression, trauma, behavior problems, evidence-based treatments, manualized treatments, cognitive-behavioral therapy, youth, mental health, self-regulation, neuroimaging

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Child STEPS
Arm Type
Experimental
Arm Description
Child STEPs includes (1) a treatment protocol, Modular Approach to Therapy for Children with Anxiety, Depression, Trauma or Conduct Problems (MATCH-ADTC), and (2) a youth monitoring and feedback system (MFS).
Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
Treatment in the UC condition will use the procedures therapists and their supervisors consider appropriate and believe to be effective, and researchers will not influence their work.
Intervention Type
Behavioral
Intervention Name(s)
Modular Approach to Therapy for Children with Anxiety, Depression, Trauma, and Conduct Problems
Other Intervention Name(s)
MATCH, MATCH - ADTC
Intervention Description
MATCH-ADTC is designed for children aged 6-15. Unlike most evidence-based treatments (EBTs), which focus on single disorder categories (e.g., anxiety only), MATCH is designed for multiple disorders and problems encompassing anxiety, depression, post-traumatic stress, and disruptive conduct, including the conduct problems associated with ADHD. MATCH is composed of 33 modules-i.e., specific treatment procedures derived from decades of research on EBTs. The various modules can be organized and sequenced flexibly to tailor treatment to each child's characteristics and needs.
Intervention Type
Other
Intervention Name(s)
Monitoring and Feedback System
Other Intervention Name(s)
MFS
Intervention Description
For each child, the web-based MFS system provides weekly monitoring of the MATCH modules used and the child's treatment response, in two forms (a) changes on the Behavior and Emotions Survey and (b) changes in severity of the top treatment concerns identified by youths and caregivers. At the end of treatment, the MFS provides a complete record of modules used, and child treatment response, across all the weeks of treatment.
Intervention Type
Behavioral
Intervention Name(s)
Treatment as usual
Other Intervention Name(s)
Usual Care, UC
Intervention Description
Treatment in the UC condition will use the procedures therapists and their supervisors consider appropriate and believe to be effective.
Primary Outcome Measure Information:
Title
Change from Baseline Emotion Regulation Task at End of Treatment
Time Frame
Change over time from Day 1 to end of treatment, assessed up to 40 weeks
Title
Change from Baseline Emotional Go/No-Go Task at End of Treatment
Time Frame
Change over time from Day 1 to end of treatment, assessed up to 40 weeks
Secondary Outcome Measure Information:
Title
Change from Baseline Attentional Bias Task at End of Treatment
Time Frame
Change over time from Day 1 to end of treatment, assessed up to 40 weeks
Title
Change from Baseline Granularity Task at End of Treatment
Time Frame
Change over time from Day 1 to end of treatment, assessed up to 40 weeks
Title
Change from Baseline Behavior Rating Inventory of Executive Function (BRIEF) at End of Treatment
Time Frame
Change over time from Day 1 to end of treatment, assessed up to 40 weeks
Title
Change from Baseline Early Adolescent Temperament Questionnaire Revised (EATQ-R) at End of Treatment
Time Frame
Change over time from Day 1 to end of treatment, assessed up to 40 weeks
Other Pre-specified Outcome Measures:
Title
Change from Baseline Coping with Children's Negative Emotions Scale (CCNES) at End of Treatment
Time Frame
Change over time from Day 1 to end of treatment, assessed up to 40 weeks
Title
Change from Baseline Parenting Stress Index-Short Form (PSI-SF) at End of Treatment
Time Frame
Change over time from Day 1 to end of treatment, assessed up to 40 weeks
Title
Change from Baseline Family Adaptability and Cohesion Scale IV (FACES-IV) at End of Treatment
Time Frame
Change over time from Day 1 to end of treatment, assessed up to 40 weeks
Title
Change from Baseline Five Minute Speech Sample (FMSS) at End of Treatment
Time Frame
Change over time from Day 1 to end of treatment, assessed up to 40 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: enrolled in grades 3-7 have a primary clinical problem in the areas of anxiety, depression, conduct, or posttraumatic stress clinically elevated problem levels on the Internalizing, Externalizing, Anxious-Depressed, Withdrawn-Depressed, Aggressive Behavior, or Rule-Breaking Behavior scales of the Child Behavior Checklist or Youth Self-Report or on the UCLA Post-Traumatic Stress Disorder Reaction Index. Exclusion Criteria: Mental retardation Pervasive developmental disorder Eating disorder children for whom attention problems or hyperactivity are the primary referral concern active psychosis and/or a suicide attempt in the previous year To participate in the two neuroimaging tasks (Emotion Regulation Task; Emotional Go/No Go Task), participants must be healthy (no major medical illness), right-handed, fluent in English, have no history of neurological impairment (including but not limited to history of loss of consciousness for great than 20 minutes, seizures, stroke, etc.), have normal or corrected to normal vision, and have no contra-indications or risk factors for MRI research (such as braces or metal implants).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John R. Weisz, PhD
Organizational Affiliation
Harvard University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Harvard University
City
Cambridge
State/Province
Massachusetts
ZIP/Postal Code
02138
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22065252
Citation
Weisz JR, Chorpita BF, Palinkas LA, Schoenwald SK, Miranda J, Bearman SK, Daleiden EL, Ugueto AM, Ho A, Martin J, Gray J, Alleyne A, Langer DA, Southam-Gerow MA, Gibbons RD; Research Network on Youth Mental Health. Testing standard and modular designs for psychotherapy treating depression, anxiety, and conduct problems in youth: a randomized effectiveness trial. Arch Gen Psychiatry. 2012 Mar;69(3):274-82. doi: 10.1001/archgenpsychiatry.2011.147. Epub 2011 Nov 7.
Results Reference
background
Citation
Chorpita, B.F., & Weisz, J.R. (2009). Modular Approach to Therapy for Children with Anxiety, Depression, Trauma, or Conduct Problems (MATCH-ADTC). Satellite Beach, FL: PracticeWise, LLC.
Results Reference
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Using Neuroimaging to Understand Children's Mental Health and Treatment Outcomes

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