- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02945384
Broader Implementation of a Successful Dual-Generation Intervention in Partnership With Head Start of Lane County
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Based on basic research on the neuroplasticity of attention, stress, and family dynamics, the investigators developed a successful dual-generation intervention that targets attention, stress, and self-regulation. The intervention has been shown to improve brain function for attention, cognition, and behavior in preschool children in Head Start (HS) and also improves communication skills and reduces stress in parents. This project involves the development of a scaled-up model of this intervention working with with Head Start of Lane County (HSOLC).
Goal 1: In partnership with HSOLC, the investigators have developed a scaled-up model of the intervention that is delivered by HS specialists and sustainable and replicable by other HS programs. This intervention is called Creating Connections: Strong Families, Strong Brains (CC).
Goal 2: To characterize the degree to which CC improves distal outcomes related to parent/family well-being by assessing health and safety outcomes in parents and children, parental education, financial literacy and decision making, household chaos, and biomarkers of allostatic load related to health outcomes.
Goal 3: To evaluate hypothesized mediating factors related to changes in family well-being, specifically changes in foundational systems (stress and self-regulation) by refining measures of family stress and self-regulation by assessing heart rate variability in parents and children and neurophysiological measures of self-regulation in parents.
Children and parents at randomly assigned HSOLC sites will receive CC, and other HSOLC sites will deliver the regular HS curriculum. The investigators hypothesize that participation in CC will result in improved brain function for attention and self-regulation as well as improved physiological function for stress regulation in both children and their parents compared to families not receiving the intervention.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Oregon
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Eugene, Oregon, United States, 97403
- University of Oregon
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Student at Head Start of Lane County (child); parent of student at HSOLC (parent)
Exclusion Criteria:
- Not a native speaker of English or Spanish
- does not have normal hearing, vision, physical, motor, and emotional development
- has history of brain injury or disorder
- currently taking medications that affect brain function
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Creating Connections
Dual-generation intervention: child component delivered in classroom setting, parent component delivered in small-group setting
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Dual-generation intervention
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No Intervention: Head Start as usual
Regular Head Start curriculum
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in brain function for selective attention: event-related potential (ERP) auditory selective attention paradigm (children and adults)
Time Frame: 3-6 months
|
To measure brain function for selective attention using ERPs, participants selectively attend to one of two simultaneously presented stories that differ in location (left/right), voice (male/female), and content.
ERPs are recorded to identical 100 msec probes embedded in stories when attended and unattended, and the effects of selective attention are quantified by comparing the brain response to probes embedded in the attended story with the response to identical probes embedded in the unattended story.
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3-6 months
|
|
Changes in stress physiology: respiratory sinus arrhythmia (parasympathetic nervous system function) and pre-ejection period (sympathetic nervous system function)
Time Frame: 3-6 months
|
RSA is an index of high-frequency beat-to-beat variability of the electrocardiogram (ECG) signal, while accounting for variability in respiration rate.
PEP is the amount of time between depolarization of the left ventricle, seen in the ECG wave as the "Q" component directly preceding a heart beat, and subsequent ejection of blood through the ventricles, measured via the maximal rate of change in the impedance waveform of the subsequent "B" component.
Baseline values of RSA and PEP will be acquired upon arrival to the lab during a five-minute neutral video of ocean scenes.
Following this, RSA and PEP will be collected during two ERP paradigms measuring selective attention (children and adults) and self-regulation (adults only).
After the tasks, physiology will be recorded during a final five-minute recovery period while a neutral video is shown.
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3-6 months
|
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Changes in child school performance: Head Start Teaching Strategies Gold assessments
Time Frame: 3-6 months
|
3-6 months
|
|
|
Changes in child behavior for cognition: language (Clinical Evaluation of Language Fundamentals-Preschool: 2nd Ed.), IQ (Stanford-Binet Intelligence Scales-5th Ed.), executive function (Snack Delay, Shape School, Noisy Book)
Time Frame: 3-6 months
|
3-6 months
|
|
|
Changes in brain function for self-regulation: event-related potential (ERP) stop-signal task paradigm (adults only)
Time Frame: 3-6 months
|
Brain function for self-regulation will be measured with an ERP variant of the stop-signal task with an added feedback component.
Each trial begins with a fixation cross for 500 ms, followed by an arrow cue pointing either left or right for 500 ms (the "go signal"), a feedback stimulus presented 400-600 ms after a response and remaining on the screen for 100 ms, and finally a jittered intertrial interval of 2000 to 4000 ms.
On 25% of trials, an auditory stop signal is played at a variable latency and adjusts trial-by-trial to appear 50 ms earlier following failed stops and 50 ms later after successful stops, while adjusting to maintain 50% response accuracy over blocks of eight stop trials.
Shorter delay between cue and stop signal for successful stops indicates better inhibitory control.
ERPs will be averaged to the onset of auditory stop signals, responses, and feedback stimuli.
|
3-6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in child social behavior: Preschool and Kindergarten Behavior Scale - 2nd Ed.
Time Frame: 3-6 months
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3-6 months
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|
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Changes in parenting behavior: videotaped parent-child interactions coded for parent language behavior using Systematic Analysis of Language Transcripts-8
Time Frame: 3-6 months
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3-6 months
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|
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Changes in parenting stress: Parenting Stress Index
Time Frame: 3-6 months
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3-6 months
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|
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Changes in home environment: Confusion, Hubbub, and Order Scale (CHAOS)
Time Frame: 3-6 months
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3-6 months
|
|
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Changes in adult health: systolic and diastolic blood pressure
Time Frame: 3-18 months
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3-18 months
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Changes in family well-being: Head Start Family Partnership Plan (FPP): Assessment of Strengths, Capabilities, & Needs
Time Frame: 3-18 months
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3-18 months
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Changes in home environment: Tayside Children's Sleep Questionnaire
Time Frame: 3-6 months
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3-6 months
|
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Changes in adult health: blood spot biomarkers of immune function
Time Frame: 3-18 months
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Immune function will be assessed via the following biomarkers: C-reactive protein, Epstein-Barr Virus antibodies, interleukin-6
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3-18 months
|
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Changes in adult health: blood spot biomarkers metabolic function
Time Frame: 3-18 months
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Metabolic function will be assessed via the following biomarkers: insulin, glycosylated hemoglobin (hemoglobin A1c) lipoprotein(a)
|
3-18 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Eric Pakulak, PhD, University of Oregon
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 03172011.022
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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