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Longitudinal Prospective Study of Maternal and Child Nutrition in Arkansas

Longitudinal Prospective Study of Maternal and Child Nutrition in Arkansas - The Thrive Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07477106
Enrollment
125
Registered
2026-03-17
Start date
2026-10-01
Completion date
2029-06-01
Last updated
2026-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infant Nutrition, Maternal Health, Maternal Nutrition, Pediatric Nutrition

Brief summary

The investigators want to learn how women's diets may impact breastfeeding outcomes. This study will help the investigators learn more about how diet and social factors like food access may impact mothers' health, breastfeeding, and their baby's health. Participants will attend a visit before birth, then 11 visits as their baby grows up. All visits will be remote using RedCap, phone or video call, text messaging or any other communication modalities of preference to the participant. The investigators will ask for personal information about participants' family, home, and finances, health literacy, medical history, current medications, pregnancy complications, mental health (depression, quality of life), confidence in breastfeeding, eating habits, and plan to feed their baby. After childbirth, the investigators will ask about participants' delivery and child's health, and request access to their child's medical records. Across all visits, the investigators will ask participants to measure their weight, height, blood pressure, activity and sleep, and child's length; the investigators will also ask them to ship urine, stool, and breast milk samples. The investigators will obtain a 24-hour feeding log for the child, as well as a log of what the mother ate and drank over 24 hours.

Interventions

None listed

Sponsors

Arkansas Children's Hospital Research Institute
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* At least 30 weeks pregnant * Ability to engage in study procedures throughout the first 12 months postpartum

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Maternal dietary intakeThird trimester of pregnancy and 0.5, 1, 2, 3, 4, 5, 6, 9, 12, 18 and 24 months postpartum24 hour dietary recall using ASA24
Child dietary pattern0.5, 1, 2, 3, 4, 5, 6, 9, 12, 18 and 24 month of age24 hour recall using NDSR
Breastfeeding outcomes0.5, 1, 2, 3, 4, 5, 6, 9, 12, 18 and 24 month postpartumExclusivity, duration and mixed feeding

Secondary

MeasureTime frameDescription
Maternal weightThird trimester and 0.5, 1, 2, 3, 4, 5, 6, 9, 12, 18 and 24 month postpartumSmart scale
Human milk composition0.5, 1, 2, 3, 4, 5, 6, 9, 12, 18, 24 month postpartum or as long as lactatingmacronutrients, micronutrients and non-nutritive components
Blood pressureThird trimester and 0.5, 1, 2, 3, 4, 5, 6, 9, 12, 18, 24 month postpartumSmart device, at home collection
Physical activityThird trimester and 0.5, 1, 2, 3, 4, 5, 6, 9, 12, 18, 24 months postpartumAccelerometry

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 29, 2026