Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
208 participants
OBSERVATIONAL
2023-06-26
2027-05-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The purpose of this study is to determine how a child's usual intake of carotenoids is related to their visual development and their blood and skin levels of carotenoids. The study involves 6 visits. For each visit, we will ask about the child's recent diet, will measure their body size, collect a blood sample, collect optical measurements of their skin, and will test how sharp their vision is.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Maternal Carotenoids Across Pregnancy Study
NCT06004479
Biological Functions of Carotenoids in Humans
NCT00356252
Feeding the Rainbow to Investigate Endothelial Dysfunction
NCT01175577
Dietary Lipids as Primary Modulators of Carotenoid Absorption in Vegetables
NCT01006174
Novel Metabolites of Beta-Carotene and Lycopene
NCT02550483
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Carotenoids are fat-soluble pigments found primarily in fruits and vegetables (F\&Vs) that support healthy functioning. Carotenoids support vitamin A requirements, reduce inflammation and cancer risk, and support cognitive, visual, and cardiovascular health. Since carotenoids are colorful, researchers can easily measure them in blood and tissues using color-measuring devices. Blood carotenoid concentrations are used as biomarkers of adult F\&V intake. Advances in carotenoid measurement technologies may make carotenoid biomarker measures in children more feasible. However, the precision and accuracy of these biomarkers in children is not as well understood.
With better measures of carotenoid intake comes the opportunity to understand how carotenoid intake relates to children's health. A high priority area to investigate in this young children is whether dietary carotenoids are associated with visual function. Lutein and zeaxanthin, carotenoids that accumulate in the back of the eye (macula), are associated with visual contrast sensitivity in children and adults, a visual function which may support children's interactions with their environments, but this association has not been sufficiently studied in healthy infants and toddlers. In this study, the investigators will define in infants and toddlers 1) the rigorous validation of a skin carotenoid biomarker of dietary intake and 2) the associations between carotenoid intake and visual function.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Observational Group
Children will be followed from 4-24 months of age.
Carotenoid Intake
Carotenoid intake calculated from food diary records reported by guardians.
Serum carotenoid concentrations
Serum carotenoid concentrations measured by HPLC.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Carotenoid Intake
Carotenoid intake calculated from food diary records reported by guardians.
Serum carotenoid concentrations
Serum carotenoid concentrations measured by HPLC.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* born at term (more than or equal to 37 weeks gestation)
* between the 1st to 99th weight for age percentile at 3 months of age
* participating guardian speaks, reads, and understands English
* guardian categorizes child as non-Hispanic white, Hispanic white, Asian, or non-Hispanic Black
Exclusion Criteria
* diagnosed food intolerance or allergy
* has a sibling enrolled in the study
3 Months
24 Months
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Houston
OTHER
East Carolina University
OTHER
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
NIH
Baylor College of Medicine
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Nancy Engelmann Moran
Assistant Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
USDA/ARS Children's Nutrition Research Center, Baylor College of Medicine
Houston, Texas, United States
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
H-52929
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.