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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05368493
Other study ID # 8232
Secondary ID R01ES032870-01
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date January 23, 2023
Est. completion date June 2027

Study information

Verified date April 2024
Source New York State Psychiatric Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study seeks to understand the relationship between prenatal maternal air pollution exposure and offspring risk for ADHD and examine two potential -modifiable- mechanisms: prenatal maternal inflammation and offspring sleep problems. We will employ a longitudinal neuroimaging study design and leverage a well-characterized intergenerational cohort of Puerto Ricans to address prior literature's limitations. This will be the first study to use infant neuroimaging to disassociate the effects of prenatal pollution exposure from those of postnatal pollution exposure, adversity and disadvantage, and offspring genetic risk for ADHD.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 182
Est. completion date June 2027
Est. primary completion date June 2027
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Months to 11 Years
Eligibility Inclusion Criteria: - Having been enrolled in the BYS-ECHO birth cohort (parent study). - Speaks English or Spanish. - Having a parent that is eligible to participate, based on criterial detailed below, and agrees to participation. - One parent must speak English or Spanish. Exclusion Criteria: - Having serious neurological disorder, excluding ASD (e.g., seizure disorder). - MRI contraindications (irremovable metal in body like braces, pacemakers). - Claustrophobia. - Having a parent that is not competent to consent (e.g., severe intellectual disability would have triggered exclusion) or under 18 years of age.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
MRI task
Task fMRI (Simon) [ Time Frame: Children will undergo MRI scans when they are 6-11 years of age. ] Children will also complete a task, which will allow exploratory analyses of the functionality of attention-related neural circuits. The Simon fMRI task is a non-verbal task equivalent to the Stroop that tests sustained attention and inhibitory control and discriminates children with and without ADHD. Exploratory fMRI time-series data for each participant will be modeled using a general linear model with 3 predictors: congruent correct, incongruent correct, and incorrect. Contrast images for each participant (e.g., incongruent-minus-congruent) will be generated and entered into a group-level random-effects model. Analyses are exploratory, and will focus on frontal lobe activity during each type of trial.

Locations

Country Name City State
United States New York State Psychiatric Institute New York New York

Sponsors (3)

Lead Sponsor Collaborator
New York State Psychiatric Institute National Institute of Environmental Health Sciences (NIEHS), University of Puerto Rico

Country where clinical trial is conducted

United States, 

References & Publications (2)

Myhre O, Lag M, Villanger GD, Oftedal B, Ovrevik J, Holme JA, Aase H, Paulsen RE, Bal-Price A, Dirven H. Early life exposure to air pollution particulate matter (PM) as risk factor for attention deficit/hyperactivity disorder (ADHD): Need for novel strategies for mechanisms and causalities. Toxicol Appl Pharmacol. 2018 Sep 1;354:196-214. doi: 10.1016/j.taap.2018.03.015. Epub 2018 Mar 14. — View Citation

Perera FP, Tang D, Wang S, Vishnevetsky J, Zhang B, Diaz D, Camann D, Rauh V. Prenatal polycyclic aromatic hydrocarbon (PAH) exposure and child behavior at age 6-7 years. Environ Health Perspect. 2012 Jun;120(6):921-6. doi: 10.1289/ehp.1104315. Epub 2012 Mar 14. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Exploratory- Task fMRI (Simon) Children will also complete a task, which will allow exploratory analyses of the functionality of attention-related neural circuits. The Simon fMRI task is a non-verbal task equivalent to the Stroop that tests sustained attention and inhibitory control and discriminates children with and without ADHD. Exploratory fMRI time-series data for each participant will be modeled using a general linear model with 3 predictors: congruent correct, incongruent correct, and incorrect. Contrast images for each participant (e.g., incongruent-minus-congruent) will be generated and entered into a group-level random-effects model. Analyses are exploratory, and will focus on frontal lobe activity during each type of trial. Children will undergo MRI scans when they are 6-11 years of age.
Primary Frontal lobe and corpus callosum volumes Frontal lobe and corpus callosum volumes in will be measure in offspring. Bilateral middle frontal cortex and corpus callosum volumes will be used in hypothesis testing. Children will be scanned either at 6-36 months or 6-11 years of age, depending on when the participants are enrolled.
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