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Enrolling by Invitation

NCT Number: NCT04398901

Neurodevelopmental Outcomes in ZIKV-Exposed Children

In this study the investigators will follow the neurodevelopmental outcome of children with in utero ZIKV exposure who do not have microcephaly or severe abnormalities consistent with Congenital Zika Syndrome. The ZIKV-exposed children will be compared to non-ZIKV exposed controls. Children will be assessed at age 3 and 4 years using standardized neurodevelopmental assessments. Children will also have neurodevelopmental assessment at age 5 and 7 years along with a brain MRI at age 7 years.

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Key information

Age range

3 year–7 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Biomelab, Barranquilla, Atlántico, Colombia

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About this study

Zika-virus (ZIKV) infection in pregnancy can result in severe brain damage in 4-12% of cases. Children exposed to ZIKV in utero during the years of 2015-2017 are now in early childhood. Children with severe neurologic injury (Congenital Zika Syndrome; CZS) have a poor developmental outcome, however the developmental outcome of apparently normal infants following in utero ZIKV-exposure is not well known. The incidence of abnormal neurodevelopmental outcome in apparently normal children with in utero ZIKV-exposure is not known.

The investigators will determine if neurodevelopmental assessment scores in children exposed to ZIKV in utero who are normal appearing differ from norms. The investigators hypothesize that ZIKV-exposed normal appearing children will have lower multi-domain developmental assessment scores compared to normative samples. The investigators hypothesize that the presence of mild postnatal non-specific cranial US findings is associated with persistent lower developmental assessment scores compared to ZIKV-exposed children who had normal cranial US and quantitative imaging will find structural and functional brain differences between ZIKV-exposed children and controls..

The investigators will perform a prospective developmental outcome study at 2 sites: 1) Department of Atlántico, Colombia through collaboration with BIOMELAB, the research center of Dr. Carlos Cure, and 2) Children's National, Washington, DC.

The objective of the study is to determine whether children who were exposed to ZIKV in utero and who do not have CZS have abnormalities in neurodevelopment during early childhood and at school age.

The primary outcome at early childhood will be neurodevelopmental assessment scores at age 3 and 4 years. Scores will be compared between Zika-exposed children and controls. The primary outcome at school age will be neurodevelopmental assessment scores at age 5 and 7 years and quantitative brain MRI at 7 years.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Zika-exposed cohort:

  • born to mothers with Zika lab confirmation by PCR, IgM, and/or PRNT, or mother was symptomatic for Zika but infection could not be excluded due to late testing and evaluated at Children's National, Washington, DC (USA) or at BIOMELAB, Barranquilla (Colombia)
  • normal fetal neuroimaging
  • normal birth head circumference
  • normal birth clinical exam
  • no more than mild non-specific postnatal cranial ultrasound or brain MRI findings during infancy (if performed)
  • able to be contacted for follow-up

Non-ZIKV exposed Controls:

  • healthy
  • no chronic medical conditions
  • no developmental concerns
  • born at term (>= 37 weeks)
  • birth date prior to March 31, 2016 (Colombian controls)

Exclusion criteria

Zika-exposed cohort:

  • another diagnosis that would impact neurodevelopment
  • abnormal brain MRI (non-specific mild findings are not an exclusion criteria)

Non-ZIKV exposed controls:

  • chronic medical condition with in-patient hospitalization since birth
  • under care of a medical specialty provider for a chronic medical condition
  • surgery with general anesthesia since birth (brief anesthesia for ear tubes, tonsillectomy, or other minor pediatric procedure is not an exclusion criteria)
  • history of seizure
  • abnormal vision (children wearing corrective lenses are eligible)
  • abnormal hearing affecting language development
  • developmental concerns expressed by caregiver
  • receiving physical, occupational, speech or developmental therapy
  • receiving special education services in school
  • behavioral or psychological condition
  • birth date March 31, 2016 or later (Colombian controls)
  • preterm birth (≤36 weeks)
  • planned relocation of child within 5 years and likely inability to complete study

Treatment and study plan

Neurodevelopmental assessments

Other

The investigators will evaluate multiple domains of neurodevelopment at age 3, 4, 5 and 7 years using parental questionnaires and child exams. At age 7 years, the children will have a non-sedated quantitative brain MRI.

Primary outcomes

  1. Neurodevelopmental assessment at age 4 years

    Time frame: 4 years of age

    PEDI-CAT score

  2. Executive function

    Time frame: 5 and 7 years of age

    BRIEF-2 score

  3. Motor function assessment

    Time frame: 5 and 7 years of age

    MABC-2 score

  4. Brain maturation

    Time frame: 7 years of age

    Quantitative brain MRI volumetric measurement

Secondary outcomes

  1. Motor function assessment

    Time frame: 4 years of age

    MABC-2 score

  2. Intellectual ability

    Time frame: 5 and 7 years of age

    Age-appropriate Wechsler

Sponsors and collaborators

Lead sponsor

Children's National Research Institute

Other

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  • National Institutes of Health (NIH)
  • Thrasher Research Fund

Registry information

Official study title

Developmental Outcome After In Utero ZIKV Exposure in Children Without Congenital Zika Syndrome

Important dates

Study start
2020
Primary completion
2025
Study completion
2025
First posted
May 21, 2020
Registry last updated
Jul 3, 2025

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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