RecruitingNCT05492708

The Heartland Study

Children's Health in the Heartland Study


Sponsor

Heartland Health Research Alliance

Enrollment

2,600 participants

Start Date

Jan 11, 2020

Study Type

OBSERVATIONAL

Conditions

Summary

The Heartland Study is a prospective, observational study that will enroll up to 2,600 pregnant participants across the Heartland States in the U.S.. The objective of the Heartland Study is to address major knowledge gaps concerning the health effects of herbicides on maternal and infant health. The study is being conducted to evaluate the associations between environmental exposures to herbicides during and after pregnancy and reproductive health outcomes. The study is measuring multiple biomarkers of herbicide exposure among pregnant Midwesterners and their partners to evaluate associations with pregnancy and childbirth outcomes, epigenetic biomarkers of exposure, and child development.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

The Heartland Study is a research cohort that follows pregnant people throughout their pregnancy and early childhood to understand how environmental, behavioral, and social factors during pregnancy affect the health of both mothers and children. Participants in 13 Midwestern US states are enrolled in their first or second trimester. You may be eligible if: • You are 18 years old or older • You are pregnant and 20 weeks and 6 days gestation or earlier • You live in one of the 13 participating states: Arkansas, Illinois, Indiana, Iowa, Kansas, Michigan, Minnesota, Missouri, Nebraska, North Dakota, Ohio, South Dakota, or Wisconsin • You can read, write, and speak English You may NOT be eligible if: • You are not fluent in English • You are unable to provide informed consent Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(4)

Indiana University Medical Center

Indianapolis, Indiana, United States

University of Iowa Health Care

Iowa City, Iowa, United States

Gundersen Health

La Crosse, Wisconsin, United States

Marshfield Clinic

Marshfield, Wisconsin, United States

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NCT05492708


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