Pilot Study of Prenatal Choline Supplementation

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-45
SponsorWayne State University

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age ≥18 yr

≤20 wk gestation

Singleton pregnancy

Abstinence from alcohol since conception (by report)

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • Placebo

    Dietary supplement

    Provided in beverage form

  • Choline bitartrate

    Dietary supplement

    Provided in beverage form.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: High-dose choline supplementationExperimental treatment 1 intervention
Group B: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Infant recognition memory

Novelty preference from the Fagan Test of Infant Intelligence

Time frame
12 months
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

Processing speed on the Fagan Test of Infant Intelligence

Time frame
12 months
2

Postnatal growth in infant length

Time frame
6.5 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Wayne State University

Lead sponsor

Columbia University

Collaborator

University of Cape Town

Collaborator