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NCT03481829Recruiting

Early Tracking of Childhood Health Determinants (ETCHED) Study

Early Tracking of Childhood Health Determinants Study

Source: ClinicalTrials.gov · Last updated 2 Nov 2026

Brief summary (registry, in English)

Background: Children s weight has increased sharply in recent years. This may put them at higher risk for health problems. High blood glucose in a pregnant mother and too much weight gain during pregnancy also may have long-term effects on the child s health. Children who become overweight or obese during childhood tend to remain so as adults. Researchers want to study many risk factors during and after pregnancy, and how these affect a child s development. They will also follow the mother s health and well-being after pregnancy. Objectives: To learn how a pregnant mother s environment, lifestyle, and health conditions may affect her child s growth and development from birth until adulthood. Eligibility: American Indian/Alaska Native (AI/AN) or Hispanic adult pregnant women and their offspring. Design: Mothers will have 3 visits during pregnancy. In the child s first year, mothers will have 2 visits and their child will have 4. Children will have 2 visits in their second year and 1 each year until they turn 18. Mothers will have a visit 2 years after birth and 4-5 years later. Both the mother and child s medical records will be reviewed. They will have physical exams and give blood and stool samples. Mothers may give cord blood and placenta samples. They will give breastmilk and urine samples. They will fill out questionnaires. They will have an ultrasound. They may get an activity monitor. Mother and child will be followed until the child s 18th birthday.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1500 (estimated)
First submitted
28 Mar 2018
Start date
14 Apr 2022
Primary completion date
31 Dec 2041
Lead sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Diseases
Obesity
NCT number
NCT03481829

What you commit to

  • Study type: Observational
  • Planned participants: 1500
  • From 14 Apr 2022 to the primary completion date, 31 Dec 2041
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • An individual who meets any of the following criteria will be excluded from participation in this study:
  • Women who are incarcerated or are unable to consent.
  • Women whose fetus is not viable or are not planning to continue the pregnancy.

Criteria the registry did not label

  • INCLUSION CRITERIA:
    • In order to be eligible to participate in this study, an individual must meet all of the following criteria:
  • Pregnant women aged 18 years or older (pregnancy confirmed by urine or serum pregnancy test, or ultrasound examination)
  • American Indian or Hispanic by self-report
  • Agree to continue with research study participation (both mother and their offspring), for at least 3 years after delivery.
    • In case where a pregnant mother is carrying multiple fetuses (multiple pregnancy), she will be eligible to participate in this study and all her live newborns, as a result of that pregnancy, will be eligible for participation in this study. Mothers will also be eligible to participate with any consecutive pregnancies.

Age in the registry: 1 day to 99 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
NIDDK, Phoenix
Coordinator of this site? Confirm its status
PhoenixUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.