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Study identifier: NCT07525193 Synced from ClinicalTrials.gov · July 29, 2026
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PREnatal Choline and Infant Outcomes Study

Condition: Nutrition During Pregnancy  ·  Sponsor: East Carolina University

PhaseNA
Planned participants102
Who can joinFemale, 18 Years to 40 Years
Healthy volunteersYes

About this study

Less than 10% of pregnant women consume adequate levels of choline, an essential nutrient for maternal lipid metabolism, placental efficiency, and fetal development. Most prenatal vitamins do not contain choline; a research survey shows that only 6% of OB/GYNs were likely to recommend choline-rich foods to pregnant women. Nutrition education grounded in the Health Belief Model (HBM) has high efficacy among pregnant women; therefore, it is likely that HBM-driven choline education intervention will increase maternal choline levels. No studies have evaluated the influence of prenatal choline education intervention on maternal, placental, and neonatal outcomes. Our preliminary data suggest that increased choline intake corresponds with lower maternal body fat percentage (BF%), infant 1-month BF%, and MSC lipid accumulation, as well as increased placental efficiency. The central hypothesis is that choline education will increase maternal choline levels and improve placental function and infant health. We will test this hypothesis with three aims: to determine the influence of choline education intervention on maternal choline intake, placental efficiency, and infant health at the whole-body and cellular levels. The proposed study will be the first to provide a critical translational understanding of the influence of prenatal choline education intervention on maternal, placental, and child health.

This description comes directly from the study's public registry record.

Talk to the study team

Ericka M Biagioni, PhD, RDN  ·  252-737-5043  ·  biagionie24@ecu.edu

Always discuss trial participation with your own doctor first.

Locations (1)

East Carolina UniversityGreenville, North Carolina, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07525193