OptiMoM Grows Up: 5.5-year Follow-up of the OptiMoM Fortifier Study

March 29, 2022 updated by: Deborah O'Connor, The Hospital for Sick Children
In Canada, the leading cause of long-term disability in children is being born at very low birth weight (VLBW). To help improve outcomes, nutrition is a modifiable aspect of infant care. Mother's milk is the optimal way to feed VLBW infants; however, many need a supplement of donor milk or preterm formula as not enough mother's milk is available. As the ideal supplement for prolonged feeding and its long-term effects is currently unknown, this study is a prospective follow-up of infants born VLBW who were fed mother's own milk or pasteurized donor breastmilk nutrient enriched with a human milk-based fortifier or a bovine protein-based fortifier. Intakes of donor milk, fortifier type, macronutrients and fatty acids will be explored. Areas of development to be assessed include: cognition, language, motor skills, and body composition. This study will also cross-sectionally examine aspects of eating behaviours, food parenting and the home environment (e.g., stress, home chaos, family functioning) with a term-born comparison. A DNA biorepository will also be created.

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Actual)

149

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

    • Ontario
      • Toronto, Ontario, Canada, M5G 0A4
        • The Hospital for Sick Children

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

5 years to 6 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Very low birth weight infants previously enrolled in the Bovine vs. Human Milk-Based Fortifier Study (NCT02137473) and a comparison group of children born full-term (>=37 weeks gestation) and weighing >2500g.

Description

Inclusion Criteria:

  • Children who were enrolled in the Bovine vs. Human Milk-Based Fortifier Study (NCT02137473)
  • Children who were born >=37 weeks gestation and weighing > 2500g [Term-born comparison group]

Exclusion Criteria:

  • For term-born comparison only: a child with any chromosomal or congenital anomaly affecting growth

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Children previously enrolled in the OptiMoM Fortifier Study
This is an observational study of children who were previously enrolled in a trial (Bovine vs. Human Milk-Based Fortifier Study) between 2014 and 2016 during which time they were randomized to have their feeds (mother's own milk or pasteurized donor breastmilk) nutrient enriched with a human milk-based fortifier or a bovine protein-based fortifier.
Participants previously enrolled in the Bovine vs. Human Milk-Based Fortifier Study
Term-born Comparison
This is an observational study of children born at full term (>= 37 weeks gestation) and weighing more than 2500g. These children will be recruited from the communities in which the OptiMoM participants live.
Children born >=37 weeks gestation and weighing more than 2500g

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Full-Scale Intelligence Quotient (IQ)
Time Frame: 5.5 years of age
Measured using the assessor-administered Wechsler Preschool and Primary Scale of Intelligence-IV (WPPSI-IV). The WPPSI-IV Full-scale IQ and all composite sub-scales are standardized to a mean of 100, with a standard deviation of 15. Higher scores indicate superior performance.
5.5 years of age
Growth
Time Frame: 5.5 years of age
Growth as assessed by weight in kilograms (kg) and height in meters (m) measured by trained staff to assess body mass index (BMI). BMI will be the ratio of weight (kg) to the square of height (m).
5.5 years of age

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Verbal Comprehension Index
Time Frame: 5.5 years of age
Measured using the assessor-administered Wechsler Preschool and Primary Scale of Intelligence-IV (WPPSI-IV). The WPPSI-IV composite sub-scales are standardized to a mean of 100, with a standard deviation of 15. Higher scores indicate superior performance.
5.5 years of age
Visual Spatial Index
Time Frame: 5.5 years of age
Measured using the assessor-administered Wechsler Preschool and Primary Scale of Intelligence-IV (WPPSI-IV). The WPPSI-IV composite sub-scales are standardized to a mean of 100, with a standard deviation of 15. Higher scores indicate superior performance.
5.5 years of age
Working Memory Index
Time Frame: 5.5 years of age
Measured using the assessor-administered Wechsler Preschool and Primary Scale of Intelligence-IV (WPPSI-IV). The WPPSI-IV composite sub-scales are standardized to a mean of 100, with a standard deviation of 15. Higher scores indicate superior performance.
5.5 years of age
Fluid Reasoning Index
Time Frame: 5.5 years of age
Measured using the assessor-administered Wechsler Preschool and Primary Scale of Intelligence-IV (WPPSI-IV). The WPPSI-IV composite sub-scales are standardized to a mean of 100, with a standard deviation of 15. Higher scores indicate superior performance.
5.5 years of age
Vocabulary Acquisition Index
Time Frame: 5.5 years of age
Measured using the assessor-administered Wechsler Preschool and Primary Scale of Intelligence-IV (WPPSI-IV). The WPPSI-IV composite sub-scales are standardized to a mean of 100, with a standard deviation of 15. Higher scores indicate superior performance.
5.5 years of age
Processing Speed Index
Time Frame: 5.5 years of age
Measured using the assessor-administered Wechsler Preschool and Primary Scale of Intelligence-IV (WPPSI-IV). The WPPSI-IV composite sub-scales are standardized to a mean of 100, with a standard deviation of 15. Higher scores indicate superior performance.
5.5 years of age
Body Composition
Time Frame: 5.5 years of age
Trained staff will measure body composition (e.g., % fat mass, % fat-free mass) using air displacement plethysmography, i.e., BODPOD™.
5.5 years of age
Body Composition
Time Frame: 5.5 years of age
Trained staff will measure body composition using bicep, tricep, subscapular and superilliac skinfold thicknesses.
5.5 years of age
Diet Quality
Time Frame: 5.5 years of age
Diet Quality as measured using the Healthy Eating Index calculated from two 24-hour recalls conducted by trained staff. Scores on the Healthy Eating Index range from 0-100 with higher scores indicated higher diet quality.
5.5 years of age
Waist circumference
Time Frame: 5.5 years of age
Trained staff will measure waist circumference (cm) at the midpoint between the top of the iliac crest and lowest rib.
5.5 years of age
Blood pressure
Time Frame: 5.5 years of age
Trained staff will measure blood pressure using an automated sphygmomanometer.
5.5 years of age

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Influence of the diet on epigenetic changes
Time Frame: 5.5 years of age
Assessed using a buccal cell biorepository.
5.5 years of age
Affect Recognition domain
Time Frame: 5.5 years of age
Measured using the assessor-administered Developmental Neuropsychological Assessment-Second Edition (NEPSY-II). Scaled scores for each subtest consist of a mean of 10 and a standard deviation of 3 (range of 1-19). Higher scores indicate superior performance.
5.5 years of age
Inhibition domain
Time Frame: 5.5 years of age
Measured using the assessor-administered Developmental Neuropsychological Assessment-Second Edition (NEPSY-II). Scaled scores for each subtest consist of a mean of 10 and a standard deviation of 3 (range of 1-19). Higher scores indicate superior performance.
5.5 years of age
Design Fluency domain
Time Frame: 5.5 years of age
Measured using the assessor-administered Developmental Neuropsychological Assessment-Second Edition (NEPSY-II). Scaled scores for each subtest consist of a mean of 10 and a standard deviation of 3 (range of 1-19). Higher scores indicate superior performance.
5.5 years of age
Statue domain
Time Frame: 5.5 years of age
Measured using the assessor-administered Developmental Neuropsychological Assessment-Second Edition (NEPSY-II). Scaled scores for each subtest consist of a mean of 10 and a standard deviation of 3 (range of 1-19). Higher scores indicate superior performance.
5.5 years of age
Visual-Motor Integration
Time Frame: 5.5 years of age
Measured using the assessor-administered Beery-Buktenica Developmental Test of Visual-Motor Integration (Beery VMI). Standard scores with a mean of 100 and a standard deviation of 15 will be reported. Higher scores on the Beery VMI indicate superior performance.
5.5 years of age
Social-Emotional Functioning
Time Frame: 5.5 years of age
Social-Emotional functioning as measured by parent-report using the Social Responsiveness Scale Second Edition (SRS-2). T-scores on the SRS-2 have a mean of 50 and standard deviation of 10. Higher scores are associated with more severe social impairments.
5.5 years of age
Behaviour and Emotional Response
Time Frame: 5.5 years of age
Behaviour and Emotional Response as measured by parent-report using the Behavior Assessment System for Children-Third Edition (BASC-3). Scores are expressed as T-scores with a mean of 50 and standard deviation of 10. Higher values indicate increased risk for composites of clinical scales and lower risk for the composite of adaptive scales.
5.5 years of age
Executive Functioning
Time Frame: 5.5 years of age
Executive Functioning as measured by parent-report using the Behavioral Rating Inventory of Executive Function (BRIEF). T-scores have a mean of 50 and a standard deviation of 10. Higher scores indicate a potential problematic area of clinical significance.
5.5 years of age
Sensory Processing
Time Frame: 5.5 years of age
Sensory Processing related to auditory, visual, touch, movement, body position and oral processing as measured by parent-report using the Sensory Profile Second Edition (Sensory Profile-2). Higher scores indicating higher sensitivity in each category.
5.5 years of age
Gross Motor Development
Time Frame: 5.5 years of age
Measured using the assessor-administered Movement Assessment Battery for Children Second Edition (Movement ABC-2). Higher scores indicate superior performance.
5.5 years of age
Influence of genetics on taste
Time Frame: 5.5 years of age
Assessed using a buccal cell biorepository.
5.5 years of age
Fatty acid status
Time Frame: 5.5 years of age
Assessed using a buccal cell biorepository.
5.5 years of age
Children's eating behaviours and dietary intake
Time Frame: 5.5 years of age
Assessed using direct observation during a standardized lunch protocol.
5.5 years of age
Children's eating behaviours
Time Frame: 5.5 years of age
Assessed by parent-report using the Child Eating Behaviour Questionnaire (CEBQ). The CEBQ is made up of eight scales: Food responsiveness, Emotional over-eating, Enjoyment of food, Desire to drink, Satiety responsiveness, Slowness in eating, Emotional under-eating, and Food fussiness. Higher scores indicate higher frequency behaviour.
5.5 years of age
Food parenting and parent dietary intake
Time Frame: 5.5 years of age
Assessed using direct observation during a standardized lunch protocol.
5.5 years of age
Food parenting
Time Frame: 5.5 years of age
Assessed by parent-report using the Comprehensive Feeding Practices Questionnaire (CFPQ). The questionnaire contains 12 scales: 'Encourage Balance and Variety', 'Environment', 'Involvement', 'Modeling', 'Monitoring', 'Teaching about Nutrition', 'Emotion Regulation', 'Food as Reward', 'Pressure', 'Child Control', 'Restriction for Health' and 'Restriction for Weight Control'; higher scores indicate higher frequency behaviour.
5.5 years of age
Composition and community structure of the gastrointestinal microbiota
Time Frame: 5.5 years of age
High-throughput sequencing of microbial DNA from stool samples
5.5 years of age
Parent and child stress
Time Frame: 5.5 years of age
Measured using cortisol levels obtained from hair samples collected from both parent and child at the posterior vertex.
5.5 years of age
Parental stress
Time Frame: 5.5 years of age
Measured by parent-report using the Parent Distress sub-scale of the Parenting Stress Index Short Form (PSI-SF). Higher scores indicate higher levels of parental distress.
5.5 years of age
Home environment- Family Functioning
Time Frame: 5.5 years of age
Family functioning will be measured by parent-report using the General Functioning sub-scale of the Family Assessment Device (FAD). Higher scores indicate lower levels of functioning (problem solving, communication, etc.).
5.5 years of age
Home environment- Home Chaos
Time Frame: 5.5 years of age
Home Chaos will be measured by parent-report using the Confusion, Hubbub and Order Scale (CHAOS). Higher scores indicate a more chaotic home environment.
5.5 years of age

Collaborators and Investigators

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

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)

March 12, 2020

Primary Completion (Actual)

December 1, 2021

Study Completion (Actual)

December 1, 2021

Study Registration Dates

First Submitted

March 11, 2020

First Submitted That Met QC Criteria

March 11, 2020

First Posted (Actual)

March 16, 2020

Study Record Updates

Last Update Posted (Actual)

March 31, 2022

Last Update Submitted That Met QC Criteria

March 29, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 1000065339

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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