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Nutritional Risk Factors for FASD in Ukraine

Primary Purpose

Fetal Alcohol Spectrum Disorders

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Prenatal multivitamin mineral supplement
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Fetal Alcohol Spectrum Disorders focused on measuring alcohol, pregnancy, infant

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • currently pregnant
  • reported alcohol consumption 4-5 drinks per occasion on 3-4 occasions in the month around conception or the most recent month of pregnancy, or
  • no more than 2 drinks per occasion in either the month around conception or the most recent month of pregnancy

Exclusion Criteria:

  • unable to provide consent
  • unable to provide information about alcohol consumption

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    No Intervention

    Arm Label

    prenatal multivitamin mineral supplement

    prenatal multivitamin mineral supplement plus choline

    Comparison

    Arm Description

    received prenatal multivitamin mineral supplement at time of enrollment TheraVit multivitamin/mineral prenatal supplement with instructions to take 1 per day through the remainder of pregnancy

    received prenatal multivitamin mineral supplement plus additional choline supplemental vitamin TheraVit multivitamin mineral supplement plus 750 mg. choline with instructions to take1 multivitamin mineral supplement and 750 mg. per day of choline through the remainder of pregnancy

    Advised to follow obstetrics standard of care which is to take a prenatal vitamin/mineral supplement

    Outcomes

    Primary Outcome Measures

    Bayley Scales of Infant Development II Mental Developmental Index
    Scaled score range 50 to 150 with higher scores indicating better performance
    Bayley Scales of Infant Development III Psychomotor Developmental Index
    Scaled score range 50 to 150 with higher scores indicating better performance

    Secondary Outcome Measures

    Full Information

    First Posted
    December 18, 2018
    Last Updated
    December 19, 2018
    Sponsor
    University of California, San Diego
    Collaborators
    National Institute on Alcohol Abuse and Alcoholism (NIAAA), Omni-Net Ukraine
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03782935
    Brief Title
    Nutritional Risk Factors for FASD in Ukraine
    Official Title
    Early Identification of Affected Children and Nutritional Risk Factors for FASD in Ukraine
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    June 2006 (undefined)
    Primary Completion Date
    June 2013 (Actual)
    Study Completion Date
    June 2013 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of California, San Diego
    Collaborators
    National Institute on Alcohol Abuse and Alcoholism (NIAAA), Omni-Net Ukraine

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Interventional study randomizing pregnant women at two sites in Ukraine who have or have not already consumed moderate to heavy levels of alcohol in pregnancy to receiving a standard prenatal vitamin supplement with or without additional choline supplement or standard of care (recommendation to take vitamin supplements) through the remainder of pregnancy, and to compare neurobehavioral performance of the offspring on the Bayley Scales of Infant Development at 12 months of age between groups. The overall sample size target was 300 alcohol exposed and 300 low or unexposed across both sites.
    Detailed Description
    Pregnant women coming in for routine prenatal diagnostic testing or prenatal care at two sites in Ukraine, Rivne Diagnostic Center or Khmelnytsky Regional Perinatal Center, were screened for alcohol consumption during pregnancy. Those who met the criteria of consuming 4-5 drinks per occasion on 3-4 occasions in either the month around conception or the most recent month of pregnancy were eligible for recruitment into the alcohol exposed group, and the next available woman who consumed no more than 2 drinks on any occasion in the month around conception or the most recent month of pregnancy was eligible for recruitment into the alcohol low or no exposure group. Within alcohol group and within site, women were randomized on a 1:1 basis to receiving a study-provided prenatal vitamin (TheraVit) manufactured in the U.S. and registered in Ukraine as an over-the-counter product, or to receiving standard of care which is obstetric advice to take prenatal vitamins on their own. Within the group randomized to receiving the prenatal vitamins, women were further randomized on a 1:1 basis to receiving an additional 750 mg. of supplemental choline manufactured in the U.S., and registered in Ukraine as an over-the-counter product. Women in both cohorts were followed until delivery and those with live born children were followed until the child reached one year of age. The primary endpoint for the intervention was performance on the mental developmental index (MDI) and the psychomotor developmental index (PDI) components of the Bayley Scales of Infant Development II. The Bayley tests were administered at approximately 12 months adjusted chronological age by trained psychologists in Ukraine. The primary comparison for the study was within the alcohol-exposed group, comparing mean Bayley scores on MDI and separately on PDI between those randomized to receiving the study prenatal vitamin and those randomized to standard of care. Secondary comparisons for the study examined the mean MDI and PDI scores on the Bayley within the alcohol-exposed group in those randomized to receiving the prenatal vitamin plus choline vs. those who received the prenatal vitamin alone the mean MDI and PDI scores on the Bayley within the low or unexposed group in those who received the prenatal vitamin vs. those who did not the mean MDI and PDI scores on the Bayley within the low or unexposed group in those who received the prenatal vitamin plus choline vs. those who received the prenatal vitamin alone adjusted comparisons for all of the above taking into account participants who were taking vitamins on their own at the time of enrollment, and/or who were taking vitamins on their own if assigned to the standard of care group.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Fetal Alcohol Spectrum Disorders
    Keywords
    alcohol, pregnancy, infant

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Pregnant women assigned to 1) over-the-counter approved prenatal multivitamin mineral supplement alone provided by the study at time of enrollment, 2)over-the-counter approved prenatal multivitamin mineral supplement with additional over-the-counter approved 750 mg choline supplement provided by the study at the time of enrollment, or 3) standard of care which is recommendation to take over-the-counter prenatal multivitamin mineral supplements
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    600 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    prenatal multivitamin mineral supplement
    Arm Type
    Experimental
    Arm Description
    received prenatal multivitamin mineral supplement at time of enrollment TheraVit multivitamin/mineral prenatal supplement with instructions to take 1 per day through the remainder of pregnancy
    Arm Title
    prenatal multivitamin mineral supplement plus choline
    Arm Type
    Experimental
    Arm Description
    received prenatal multivitamin mineral supplement plus additional choline supplemental vitamin TheraVit multivitamin mineral supplement plus 750 mg. choline with instructions to take1 multivitamin mineral supplement and 750 mg. per day of choline through the remainder of pregnancy
    Arm Title
    Comparison
    Arm Type
    No Intervention
    Arm Description
    Advised to follow obstetrics standard of care which is to take a prenatal vitamin/mineral supplement
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Prenatal multivitamin mineral supplement
    Other Intervention Name(s)
    Prenatal multivitamin mineral supplement plus choline supplement
    Intervention Description
    prenatal vitamin/mineral supplement with or without choline supplement
    Primary Outcome Measure Information:
    Title
    Bayley Scales of Infant Development II Mental Developmental Index
    Description
    Scaled score range 50 to 150 with higher scores indicating better performance
    Time Frame
    approximately 12 months of age adjusted for preterm delivery
    Title
    Bayley Scales of Infant Development III Psychomotor Developmental Index
    Description
    Scaled score range 50 to 150 with higher scores indicating better performance
    Time Frame
    approximately 12 months of age adjusted for preterm delivery

    10. Eligibility

    Sex
    Female
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: currently pregnant reported alcohol consumption 4-5 drinks per occasion on 3-4 occasions in the month around conception or the most recent month of pregnancy, or no more than 2 drinks per occasion in either the month around conception or the most recent month of pregnancy Exclusion Criteria: unable to provide consent unable to provide information about alcohol consumption

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    This study is part of a collaborative initiative on Fetal Alcohol Spectrum Disorders and de-identified data is available to share with other researchers on a specified timetable with appropriate application for use.
    IPD Sharing Time Frame
    2020 and indefinitely
    IPD Sharing Access Criteria
    Application to Collaborative Initiative on Fetal Alcohol Spectrum Disorders data oversight group at CIFASD.org
    IPD Sharing URL
    http://cifasd.org

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    Nutritional Risk Factors for FASD in Ukraine

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