Effects of Prenatal DHA Supplements on Infant Development

June 6, 2022 updated by: Usha Ramakrishnan, Emory University
This research study research is about the significance of polyunsaturated fatty acids (PUFAs) for human development. Specifically, the study team will assess the effect of docosahexanoic acid (DHA) supplementation during pregnancy on infant growth and development through a randomized controlled intervention trial in Cuernavaca, Mexico. This is a collaborative effort between the Rollins School of Public Health, Emory University, the Instituto Nacional de Salud Publica (INSP) and the Instituto Mexicano del Seguro Social (IMSS), Cuernavaca, Mexico. Pregnant women attending the IMSS General Hospital I are recruited between 18-22 weeks gestation and assigned randomly to receive either DHA (400 mg) or a placebo daily until delivery. The main study outcomes include a) birth outcomes: birth size, gestational age, cord blood levels of DHA and neurodevelopment b) maternal blood and breast milk DHA levels at 1 and 3 months post-partum, c) postnatal growth and development during the first 5 years of age and d) infant DHA status at 3, 12 and 18 months.

Study Overview

Status

Completed

Conditions

Detailed Description

This research study is about the significance of polyunsaturated fatty acids (PUFAs) for human development. Specifically, the study team will assess the effect of docosahexanoic acid (DHA) supplementation during pregnancy on infant growth and development through a randomized controlled intervention trial in Cuernavaca, Mexico. This is a collaborative effort between the Rollins School of Public Health, Emory University, the Instituto Nacional de Salud Publica (INSP) and the Instituto Mexicano del Seguro Social (IMSS), Cuernavaca, Mexico. Pregnant women attending the IMSS General Hospital I are recruited between 18-22 wks gestation and assigned randomly to receive either DHA (400 mg) or a placebo daily until delivery. The main study outcomes include a) birth outcomes: birth size, gestational age, cord blood levels of DHA and neurodevelopment b) maternal blood and breast milk DHA levels at 1 and 3 mo post-partum c) postnatal growth and development during the first 5 years of age and d) infant DHA status at 3, 12 and 18 mo. All data collection is carried out at the study headquarters (IMSS) except for home environment that is assessed during home visits. Physical growth (length, weight, and head circumference) and infant and child development (visual and auditory evoked potentials, visual attention, Bayley scales of infant development, McCarthy child development score, Hearts and Flowers stroop test, and other computerized child development tests) are measured at birth, 1, 3, 6, 9, 12, 18, 24, 36 months and at 4 and 5 years of age by trained workers. Data are also obtained on socioeconomic status, obstetric history, maternal diet, anthropometry and intelligence, quality of home environment and infant feeding practices. Data analysis will include group comparisons (intent-to-treat) after ensuring effectiveness of randomization, and structural equation modeling to examine the various pathways by which DHA supplementation during pregnancy affects child growth and development. The findings of this project will contribute significantly to our understanding of the functional consequences of DHA supplementation during pregnancy.

Study Type

Interventional

Enrollment (Actual)

1094

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Morelos
      • Cuernavaca, Morelos, Mexico
        • IMSS General Hospital I

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • 18-22 weeks pregnant (based on last menstrual period)
  • 18 - 35 years old
  • Resident of Cuernavaca who intends to deliver at the IMSS General Hospital I and remain in the area for the 2 years following recruitment
  • Intends to predominantly breastfeed infant until 3 months of age
  • Agrees to participate with informed consent

Exclusion criteria

  • High risk pregnancy: If documented in the clinical record at recruitment and will include history and prevalence of abruptio placentae, any serious bleeding episode in the current pregnancy, gestational diabetes, pregnancy induced hypertension, maternal toxoplasmosis infection during pregnancy, coagulation disorders, thrombocytopenia or chronic vascular, renal or systemic disease and drug use.
  • Lipid metabolism (hyperlipidemia) and/or absorption disorders
  • Regular intake of fish oil or DHA supplements during pregnancy
  • Chronic use of medication for illnesses like epilepsy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: DHA arm
Docosahexonic acid (DHA) (400 mg/day). Pregnant women attending the IMSS General Hospital I are recruited between 18-22 wks gestation and assigned randomly to receive either DHA (400 mg) or a placebo daily until delivery.
400 mg/d of docosahexanoic acid (DHA) during pregnancy
Other Names:
  • Martek Algal DHA
Placebo Comparator: Placebo arm
Pregnant women attending the IMSS General Hospital I are recruited between 18-22 wks gestation and assigned randomly to receive either DHA (400 mg) or a placebo daily until delivery.
2 tablets daily during pregnancy
Other Names:
  • Specially formulated by Martek Biosciences

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Birth size
Time Frame: Birth
Birth size will be determined by measuring the newborn, a baby's length is measured from the top of their head to the bottom of one of their heels.
Birth
Gestational age
Time Frame: Birth
Gestational age is measured in weeks, from the first day of the woman's last menstrual cycle to the current date.
Birth
Changes in visual evoked potentials
Time Frame: 3 and 6 months of age
Visual evoked potential (VEP) is an electrical signal emanated from the brain while a visual stimulus is presented to the subject in a time locked manner. The VEP can be used as a diagnostic tool to detect ocular diseases in patients with visually impaired. VEP response can also be used to detect eye diseases like glaucoma, diabetic retinopathy, multiple sclerosis, ocular hypertension, loss of peripheral (side) vision, macular degeneration and color blindness.
3 and 6 months of age
Changes in infant weight
Time Frame: Birth, months 1, 3, 6, 9, 12, 18, 24, 36 and at 4 and 5 years of age
Infant weight is measured in kilograms (kg) and weight is measured in the hospital and at all check-ups.
Birth, months 1, 3, 6, 9, 12, 18, 24, 36 and at 4 and 5 years of age
Changes in infant height
Time Frame: Birth, months 1, 3, 6, 9, 12, 18, 24, 36 and at 4 and 5 years of age
Infants will be measured in the hospital and at all check-ups. Height is measured in centimeters (cm).
Birth, months 1, 3, 6, 9, 12, 18, 24, 36 and at 4 and 5 years of age
Changes In infant head circumference
Time Frame: Birth, months 1, 3, 6, 9, 12, 18, 24, 36 and at 4 and 5 years of age
Head circumference or OFC [occipital frontal circumference] is measured over the most prominent part on the back of the head (occiput) and just above the eyebrows (supraorbital ridges). This can be translated to mean the largest circumference of the head. Head circumference is measured in centimeters (cm).
Birth, months 1, 3, 6, 9, 12, 18, 24, 36 and at 4 and 5 years of age
Changes in auditory evoked potentials
Time Frame: 1 and 3 months of age
A brainstem auditory evoked response (BAER) test measures how the brain processes the sounds a person hears. The BAER test records the subject's brainwaves in response to clicks or other audio tones that are played for them.
1 and 3 months of age
Changes in child development score
Time Frame: 1, 1.5 and 5 years of age
The Bayley Scales of Infant Development -II are used to assess child development during the first two years of life while The McCarthy Scales of Children's Abilities (MSCA) is a psychological instrument for young children that measures cognitive ability in six domain areas: Verbal, Perceptual-Performance, Quantitative, General Cognitive, Memory, and Motor at age 5 y.
1, 1.5 and 5 years of age
Changes in Hearts and Flowers Stroop Test
Time Frame: 5 years of age
This tests working memory, response inhibition, and task switching/cognitive flexibility . The task requires participants to press a response button that is either on the same side (congruent) or opposite side (incongruent) of an image. When children see an image of a heart, they are instructed to press the corresponding directional arrow button on a keyboard. When children see an image of a flower, they are instructed to press the opposite directional arrow button on the keyboard . The task consists of three separate levels that contain only congruent trials (12 trials total), only incongruent trials (12 trials total), and mixed congruent and incongruent trials respectively (33 trials total). Images are presented on a computer monitor. Before both the congruent and incongruent trial blocks, a training period is administered which consists of 5 trials. The child is unable to advance to the next question until they respond correctly.
5 years of age

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes Immune function
Time Frame: first 6 months of life
first 6 months of life
Changes in Morbidity
Time Frame: Birth, months 1, 3, 6, 9, 12, 18, 24, 36 and at 4 and 5 years of age
Changes in morbidity (health) factors will be assessed.
Birth, months 1, 3, 6, 9, 12, 18, 24, 36 and at 4 and 5 years of age
Cognitive outcomes at age 7 years of age
Time Frame: At 7 year follow up
The cognitive intelligence test WAIS-IV offers compound scores that reflect the intellectual functioning of 4 cognitive areas (verbal understanding, perceptive reasoning, working memory and processing speed). It also offers a compound score that reflects intellectual aptitude in general (Intelligence quotient).
At 7 year follow up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2005

Primary Completion (Actual)

January 3, 2013

Study Completion (Actual)

August 16, 2014

Study Registration Dates

First Submitted

March 25, 2008

First Submitted That Met QC Criteria

March 25, 2008

First Posted (Estimate)

March 28, 2008

Study Record Updates

Last Update Posted (Actual)

June 7, 2022

Last Update Submitted That Met QC Criteria

June 6, 2022

Last Verified

June 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • IRB00024976
  • 5R01HD043099 (U.S. NIH Grant/Contract)
  • 5R03HD087606 (U.S. NIH Grant/Contract)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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