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NCT Number: NCT07699393

Pilot Study of Prenatal Choline Supplementation

A double-blind, randomized, placebo-controlled trial (RCT; NCT04395196) of prenatal choline supplementation is ongoing (1) to assess the effectiveness of maternal choline supplementation during pregnancy to mitigate effects of PAE on three primary outcomes: infant recognition memory and postnatal growth restriction (weight and head circumference); (2) to assess the efficacy of this supplementation for mitigating alcohol effects on the following secondary outcomes: infant eyeblink conditioning, postnatal length, and information processing speed. The study design was based on a pilot feasibility study in 70 heavy-drinking pregnant women. Infants in the choline-treated arm were more likely to meet criterion for eyeblink conditioning than those in the placebo arm. Infants born to both the choline- and placebo-treated mothers were small at birth, but those in the choline arm showed considerable catch-up growth in weight and head circumference by 6.5 months, which persisted through 12 months. At 12 months, infants in the choline arm showed markedly better recognition memory compared to placebo-treated on the Fagan Test of Infant Intelligence, which is known to have predictive validity for school-age IQ. Of note, infants with heavy prenatal alcohol exposure whose mothers were in the active choline treatment arm performed better on FTII novelty preference neurobehavioral testing than infants in an observational study that was running in parallel who had no prenatal alcohol exposure. These pilot findings indicate that any beneficial effects of prenatal choline supplementation seen may be due in part or entirely due to general beneficial effects on fetal brain development rather than mechanisms that are specific to the teratogenic effects of alcohol. Thus, the aim of this pilot study is to enroll and randomize 50 alcohol-abstaining pregnant women to participate in an identical study protocol (same study procedures and primary and secondary outcomes) to NCT04395196, which includes only alcohol-consuming pregnant women. Effect sizes between this pilot, non-drinking group and the larger study of alcohol-consuming women will be compared to explore the degree to which prenatal choline supplementation benefits growth and neurobehavior in infants without prenatal alcohol exposure and to explore the degree to which beneficial treatment effects of choline are specific to prenatal alcohol exposure.

Recruiting

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

About this study

The study protocol will be identical to NCT04395196 except for sample size (goal = 50 pregnant women and their infants) and that instead of including heavy-drinking pregnant women, inclusion criteria require that women have fully abstained from alcohol during pregnancy at the time of randomization. All other inclusion/exclusion criteria and study procedures are identical.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥18 yr
  • ≤20 wk gestation
  • Singleton pregnancy
  • Abstinence from alcohol since conception (by report)
  • Current choline dietary intake <1 g/day
  • Language fluency in English or Afrikaans

Exclusion criteria

  • Use of methamphetamine or other illicit drugs other than marijuana during the past year
  • HIV positive
  • Pharmacologic treatment for a serious pre-existing medical condition (e.g., diabetes, hypertension, epilepsy, or cardiac problems)
  • Having another child enrolled in the trial from a previous pregnancy
  • Plans for mother or child to move away from the area prior to study completion

Treatment and study plan

Placebo

Dietary Supplement

Provided in beverage form

Choline bitartrate

Dietary Supplement

Provided in beverage form.

Primary outcomes

  1. Infant recognition memory

    Time frame: 12 months

    Novelty preference from the Fagan Test of Infant Intelligence

  2. Postnatal infant weight gain

    Time frame: 6.5 months

  3. Postnatal growth in infant head circumference

    Time frame: 6.5 months

Secondary outcomes

  1. Infant information processing speed

    Time frame: 12 months

    Processing speed on the Fagan Test of Infant Intelligence

  2. Postnatal growth in infant length

    Time frame: 6.5 months

Study contacts

Contact information is provided by the study sponsor or research team.

R. Colin Carter, MD, MMSc

CONTACT

[email protected]

+12123052995

Sandra W Jacobson, PhD

CONTACT

[email protected]

+13139935454

Sponsors and collaborators

Lead sponsor

Wayne State University

Other

Collaborators

  • Columbia University
  • University of Cape Town

Registry information

Official study title

A Randomized, Double-Blind, Placebo-controlled Clinical Trial of Choline Supplementation During Pregnancy to Mitigate Adverse Effects of Prenatal Alcohol Exposure on Growth and Cognitive Development: Pilot Arm for Non-Drinking Women

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
Jul 13, 2026
Registry last updated
Jul 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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