RECRUITING

PRenatal and Obstetric Maternal Exposures and ISlet Autoantibodies in Early Life

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This research study is called 'PRenatal and Obstetric Maternal Exposures and ISlet Autoantibodies in Early Life: The PROMISE Study'. The purpose of this study is to find out more about how exposures during pregnancy, such as having an infection, diet and growth may impact later risk of type 1 diabetes (TID) and islet autoimmunity in the child. We are also interested in finding out more about why having a father or sibling with T1D increases risk of autoimmunity in the child more than having a mother with T1D. We are enrolling women who are pregnant and either have T1D or another first degree relative (father or full sibling) of the baby has T1D. The biological father is also invited to enroll in study, as it is important to understand how the father's health and genetics may contribute to the child's risk of developing T1D. The study procedures for the mother, father and baby are explained below. Mother: Pregnant women will be asked to complete a visit once per trimester (3 visits) during pregnancy and one visit up to 12 weeks after delivery. At each visit, mothers will consent to a blood draw, collection of biological samples and the completion of questionnaires. . Mothers who have T1D will also be asked to download any diabetes device data they have, such as continuous glucose monitor or insulin pump data. Father: The (biological) father will be invited to enroll in a single visit. He will consent to a blood draw and completion of questionnaires. Fathers with T1D will also be asked to download any diabetes device data they have, such as continuous glucose monitor or insulin pump data. Baby: The baby will have blood collected at birth to determine the genetic risk for T1D. Families will consent to the completion of questionnaires about growth, health and diet at 6, 12, 18 and 24 months of age and between 5-7 years of age, and to complete blood testing for islet autoantibodies at 24 months and between 5-7 years of age. For those children with a high genetic risk score, we will also collect blood for autoantibody testing at 6, 12, and 18 months of age.

Official Title

PRenatal and Obstetric Maternal Exposures and ISlet Autoantibodies in Early Life

Quick Facts

Study Start:2022-12-01
Study Completion:2032-11-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06141434

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.

Ages Eligible for Study:0 Days to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Pregnant women and their offspring where the offspring has a first degree relative (mother, biological father, full sibling) with type 1 diabetes
  2. * Mother is 18 or older
  3. * Mother is both gestational and biological mother
  4. * Gestation up to 24 weeks at enrollment
  1. * Parents do not agree to inclusion of the offspring in the study and genetic risk testing
  2. * Greater than singleton pregnancy

Contacts and Locations

Study Contact

JANET K SNELL-BERGEON, PhD, MPH
CONTACT
7208917122
Janet.Snell-Bergeon@cuanschutz.edu
Catherine Chartier-Logan, MPH
CONTACT
3037247505
Catherine.Chartier-Logan@cuanschutz.edu

Principal Investigator

JANET K SNELL-BERGEON, PhD, MPH
PRINCIPAL_INVESTIGATOR
University of Colorado, Denver

Study Locations (Sites)

University of Colorado
Aurora, Colorado, 80045
United States
Joslin Diabetes Center
Boston, Massachusetts, 02215
United States
Mt Sinai
New York, New York, 10029
United States
Ohio State University
Columbus, Ohio, 43081
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

  • JANET K SNELL-BERGEON, PhD, MPH, PRINCIPAL_INVESTIGATOR, University of Colorado, Denver

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 Registration Dates

Study Start Date2022-12-01
Study Completion Date2032-11-30

Study Record Updates

Study Start Date2022-12-01
Study Completion Date2032-11-30

Terms related to this study

Additional Relevant MeSH Terms

  • Type 1 Diabetes
  • Pregnancy in Diabetic