- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06139874
Thrive Intervention in Schools
Promoting Emotional Development Among Young Children Facing Adversity: An Effectiveness Implementation Study in St. Louis Schools
This study is designed to test the effectiveness and implementation of an early intervention therapy for children and their primary caregivers by using existing school counselors across several school districts.
The intervention is a 6-8 week caregiver-child intervention (THRIVE) which will be conducted via video conference in the family's home (i.e., zoom), or within the school setting (or a combination of those 2 modalities depending upon feasibility for the family). THRIVE will be compared to an asynchronous on-line parenting education program, Parenting Wisely (PW). This online parenting course will be accessed at www.parentingwisely.com.
Existing school counselors will be trained in the delivery of THRIVE to 3-7 year old children (in preschool, kindergarten and first grade) and their primary caregivers. In addition to testing the effectiveness of THRIVE compared to PW, we will also compare two implementation strategies: THRIVE-Coached and THRIVE-Low Coached (LC). We will assess ongoing coaching of THRIVE trainees to increase therapist efficacy and adherence to the intervention (THRIVE-Coached). This will be compared to implementation of THRIVE with low supports (e.g. weekly supervision) provided only for the first case following the initial training (THRIVE-LC].
Compared to those randomized to PW, we expect children who receive THRIVE will have significantly better behavioral and socio-emotional outcomes. Caregivers who receive THRIVE will experience less parenting stress and depression, more optimism and will show more nurturing, emotional tolerance, and supportive caregiving.
Therapists in the THRIVE-Coached condition will deliver the intervention with higher achieved outcomes and find the intervention to be more acceptable than therapists in the THRIVE-LC condition. Therapists in the THRIVE-Coached condition will be more likely to plan to sustain the intervention following the completion of the study than those in the THRIVE-LC condition. Parents and children receiving THRIVE from therapists in the THRIVE-Coached condition will have better socio-emotional outcomes than those in the THRIVE-LC and PW conditions.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Missouri
-
St Louis, Missouri, United States, 63108
- Early Emotional Development Program
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Near the clinical threshold on the Teacher or Parent Report Form
- An active primary caregiver can be identified and is available to participate in the intervention (mother, father, grandparent or any adult in this role)
Exclusion Criteria:
- Autism
- Major neurological disorder
- Participating in active weekly individual or family therapy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: THRIVE Coached
Thrive is a promising early intervention for depression that directly targets developing affective systems and builds on the empirical literature on emotion development and prevention.
It will be delivered by school social workers/counselors.
Following training in THRIVE, school therapists in this condition will receive ongoing weekly group supervision over the life of the study.
|
Early intervention for depression that directly targets developing affective systems and builds on the empirical literature on emotion development and prevention.
|
|
Experimental: THRIVE Low Coached
Thrive is a promising early intervention for depression that directly targets developing affective systems and builds on the empirical literature on emotion development and prevention.
It will be delivered by school social workers/counselors.
Following training in THRIVE, school therapists in this condition will receive weekly group supervision only during thier first THRIVE case.
|
Early intervention for depression that directly targets developing affective systems and builds on the empirical literature on emotion development and prevention.
|
|
Active Comparator: Parenting Wisely
Online asynchronous parenting training that parents will complete independently.
|
Online asynchronous parenting program.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child Behavior Checklist
Time Frame: T1 (baseline), T2 (halfway through intervention), T3 (completion of intervention) and T4 (12 weeks post intervention)
|
Measure of child psychopathology/impairment (emotional and behavioral functioning).
Raw scores are converted into T-scores.
The T-scores range from 50 to 100, with higher scores indicating more problematic behaviors.
T-scores above 65 indicate psychiatric symptoms.
|
T1 (baseline), T2 (halfway through intervention), T3 (completion of intervention) and T4 (12 weeks post intervention)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Emotion Regulation Checklist
Time Frame: T1 (baseline), T3 (completion of intervention)
|
Measure of children's self-regulation that targets affective lability, intensity, valence, and flexibility.
The total scores range from 24 to 96, with higher scores indicating better emotion regulation.
|
T1 (baseline), T3 (completion of intervention)
|
|
Coping with Children's Negative Emotions Scale
Time Frame: T1 (baseline), T2 (halfway through intervention), T3 (completion of intervention)
|
Measure of parental coping styles in response to children's negative emotions.
It consists of six subscales: Distress Reactions, Punitive Reactions, Expressive Encouragement, Emotion-Focused Reactions, Problem-Focused Reactions, and Minimization Reactions.
The scores of each subscale range from 12 to 84, with higher scores indicating a greater likelihood of the parent engaging the type of response measured by that subscale.
|
T1 (baseline), T2 (halfway through intervention), T3 (completion of intervention)
|
|
Parenting Stress Index
Time Frame: T1 (baseline), T3 (completion of intervention)
|
Measure of potential dysfunctional parent-child relationships and severity of parenting stress.
Higher scores indicate higher levels of stress.
|
T1 (baseline), T3 (completion of intervention)
|
|
Parent-Child Observed Interaction Coding
Time Frame: T1 (baseline), T3 (completion of intervention)
|
Objective ratings of the parent-child relationship functioning, parent emotion learning and child emotional competence.
|
T1 (baseline), T3 (completion of intervention)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Beck Depression Inventory-II
Time Frame: T1 (baseline), T3 (completion of intervention)
|
Measure of parental depression.
The total scores range from 0 to 63, with higher scores indicating more severe symptoms.
|
T1 (baseline), T3 (completion of intervention)
|
Collaborators and Investigators
Investigators
- Principal Investigator: Joan Luby, PhD, Washington University School of Medicine
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202306092
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.
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