- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05135728
Development and Pilot Testing of a Novel Preschool Executive Function Curriculum
August 19, 2024 updated by: Allison Ratto, Children's National Research Institute
Development and Pilot Testing of a Novel Preschool Executive Function Curriculum Development of an Executive Function Intervention for Adolescents With Autism Spectrum Disorders
Executive function (EF) skills are a set of essential cognitive abilities that enable individuals to demonstrate their knowledge and talents, effectively complete tasks and navigate social interactions through flexible regulation of their thinking, behavior and emotions.
EF is strongly linked to academic readiness and long-term educational outcomes.
Children's EF is impacted by poverty-related experiences and is also impaired in the increasing number of children with developmental and emotional disabilities.
Interventions targeting EF skills hold particular promise for improving children's educational trajectories by leveraging brain plasticity in the preschool period.
We will directly target EF skills in preschoolers with poor EF.
This project will address a key source of the achievement gap by meeting the needs of children at the highest risk, those who: 1) show early signs of EF impairment; 2) live in low-income communities and 3) are at risk for developmental and emotional disabilities (DD/ED).
The intervention is a downward extension of Unstuck and On Target for elementary school (UOT; Cannon, Kenworthy, Alexander, Werner, & Anthony, 2018), an EF intervention shown to be effective at increasing children's learning behaviors, as delivered by school staff.
The research team will partner with key stakeholders to revise and iteratively refine UOT-P through a development trial, utilizing participant, teacher and parent feedback.
The results of this trial will be leveraged to enable the team to apply for future federal funding for a randomized comparative effectiveness trial (NIH, Institute of Educational Sciences, Patient-Centered Outcomes Research Institute).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
63
Phase
- Not Applicable
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
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Maryland
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Silver Spring, Maryland, United States, 20901
- Children's National Hospital
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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 6 years (Child)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
Enrolled as a student at a participating school site OR as a patient at a participating clinic site
- Chronological age between 3-6 years at enrollment
- English as a primary language
- Roughly age-appropriate core language skills as determined by referring school staff or provider
- Identified by school staff or provider as having problems with flexibility
Exclusion Criteria:
No longer enrolled at participating school or clinic site
• Insufficient English fluency or language skills to complete intervention
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: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Unstuck and On Target-Preschool
UOT-P is based on the foundational principles of UOT for improving EF as well as evidence-based teaching methods (e.g., positive behavior supports, visual aids).
Through this program, children, teachers and parents develop a shared self-regulatory vocabulary that enables children to improve EF at home and school through adult modeling and gradual scaffolding.
The self-regulatory vocabulary (e.g., Flexible, Make a New Plan, Unstuck) becomes a "contagious" common language.
We hypothesize this is the mechanism of change by which children will show improved EF skills, leading to increased academic readiness, improved social competence and reduced externalizing behaviors.
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Unstuck & On Target: Preschool (UOT:P) is a group-based curriculum for preschool and kindergarten students that targets executive function skills using CBT techniques.
The UOT-P curriculum consists of 16 child small-group or classroom-wide lessons.
Each lesson follows a clear structure in which the theme for the session is introduced in a storybook, supported with manipulatives and visuals.
Children implement the skills introduced in the storybook through joing play activities that require them to flexibly adjusting their plans to work together.
Children learn key vocabulary and active coping and problem-solving skills, with adult modeling and scaffolding, that enable them to build early executive functioning skills for self-regulation and classroom participation.
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Active Comparator: Waitlist Control
Children at clinic sites beginning in Year 4 will be placed in Arm 2, in which a waitlist control model will be used.
Assessment of participants on outcome measures will occur at pre-intervention, followed by a 16-week waitlist period, again at baseline, followed by a 16-week intervention, and then finally at endpoint.
All participants in Arm 2 will receive UOT-P as their intervention (see Experimental Arm).
|
Unstuck & On Target: Preschool (UOT:P) is a group-based curriculum for preschool and kindergarten students that targets executive function skills using CBT techniques.
The UOT-P curriculum consists of 16 child small-group or classroom-wide lessons.
Each lesson follows a clear structure in which the theme for the session is introduced in a storybook, supported with manipulatives and visuals.
Children implement the skills introduced in the storybook through joing play activities that require them to flexibly adjusting their plans to work together.
Children learn key vocabulary and active coping and problem-solving skills, with adult modeling and scaffolding, that enable them to build early executive functioning skills for self-regulation and classroom participation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility of Intervention
Time Frame: Through study completion, average of 20 weeks
|
Interventionist ratings of feasibility will serve as the primary outcome measure.
Interventionists will rate overall intervention feasibility using the Feasibility of Intervention Measure (FIM) at outcome.
Scores range 4-20, where higher scores indicate higher feasibility.
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Through study completion, average of 20 weeks
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Feasibility - Child Attendance
Time Frame: Through study completion, average of 20 weeks
|
Child attendance at groups will also be tracked.
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Through study completion, average of 20 weeks
|
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Acceptability of Intervention
Time Frame: Through study completion, average of 20 weeks
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Acceptability will be measured via interventionist ratings on the Acceptability of Intervention Measure (AIM).
Scores range from 4-20, where higher scores indicate higher acceptability.
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Through study completion, average of 20 weeks
|
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Intervention Appropriateness
Time Frame: Through study completion, average of 20 weeks
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Acceptability will be measured via interventionist ratings on the the Intervention Appropriateness Measure (IAM) at outcome.
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Through study completion, average of 20 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Fidelity Observations
Time Frame: twice throughout intervention period, average of 6 weeks between observations
|
The Unstuck Treatment Implementation Measure will be used to assess interventionist fidelity.
Standardized observations will be conducted, with ratings of fidelity on a Likert scale across several dimensions.
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twice throughout intervention period, average of 6 weeks between observations
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Interventionist Knowledge
Time Frame: baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
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Interventionist knowledge of executive functioning and intervention strategies will be assessed using a five-item multiple-choice survey.
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baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child Behavior Rating Scale (CBRS)
Time Frame: baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
|
This is a development trial, and thus primary outcomes assess feasibility and acceptability.
However, preliminary investigation of child-level outcomes will also be undertaken.
Classroom teachers will respond complete the CBRS, which uses a Likert scale to rate children's classroom behaviors for engagement with academic tasks, adults, and peers.
|
baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
|
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Head-Toes-Knees-Shoulders Revised (HTKS-R)
Time Frame: baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
|
This is a development trial, and thus primary outcomes assess feasibility and acceptability.
However, preliminary investigation of child-level outcomes will also be undertaken.
Trained assessors will administer the HTKS-R to child participants, which assesses self-regulation and emerging executive functioning.
The HTKS-R is a short (5-8 minutes) behavioral task that assess children's working memory and impulse control through a short game in which children are introduced to paired body parts and instructed to touch the opposite body part of the one named.
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baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
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Differential Ability Scales-II (DAS-II): Pattern Construction
Time Frame: baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
|
This is a development trial, and thus primary outcomes assess feasibility and acceptability.
However, preliminary investigation of child-level outcomes will also be undertaken.
The Pattern Construction subtest of the DAS-II will be administered to child participants.
It requires children to replicate a visual design with blocks under timed conditions.
Performance on this task is correlated with executive functioning abilities.
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baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
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Classroom Observations
Time Frame: baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
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This is a development trial, and thus primary outcomes assess feasibility and acceptability.
However, preliminary investigation of child-level outcomes will also be undertaken.
Trained evaluators will observe child participants' behavior over the course of 10-15 minutes in the classroom.
Behaviors directly targeted in the intervention will be coded using a yes/no rating to indicate the presence or absence of a problem behavior during the observation.
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baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
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Behavior Rating Inventory of Executive Functioning-Preschool (BRIEF-P): Selected subscales
Time Frame: baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
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This is a development trial, and thus primary outcomes assess feasibility and acceptability.
However, preliminary investigation of child-level outcomes will also be undertaken.
Parent report of child participant behavior on the Shift and Emotional Control subscales of the BRIEF-P (an age-normed parent report measure of daily executive functioning problems in preschoolers) will be used to assess change in daily executive functioning skills.
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baseline, end of intervention - an average of 20 weeks between baseline and end of intervention
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Lauren Kenworthy, Children's National
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 (Actual)
November 15, 2021
Primary Completion (Actual)
August 1, 2024
Study Completion (Actual)
August 1, 2024
Study Registration Dates
First Submitted
October 6, 2021
First Submitted That Met QC Criteria
November 15, 2021
First Posted (Actual)
November 26, 2021
Study Record Updates
Last Update Posted (Actual)
August 21, 2024
Last Update Submitted That Met QC Criteria
August 19, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Pro00014103
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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