TrialNet Pathway to Prevention of T1D
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 2 Years to 45 Years
- Sex
- All sexes
- Healthy volunteers
- Accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
- Procedures mentioned: Blood draws
Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.
Show the study's own words
- "Detailed Description: The Pathway to Prevention Study is conducted in two parts: * Screening * Monitoring (annual and semi-annual depending on risk) In Screening , a simple blood test is done to screen for the presence of diabetes-related biochemical autoantibodies (GAD and mIAA)."
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
Rationale: The accrual of data from the laboratory and from epidemiologic and prevention trials has improved the understanding of the etiology and pathogenesis of type 1 diabetes mellitus (T1DM). Genetic and immunologic factors play a key role in the development of T1DM, and characterization of the early metabolic abnormalities in T1DM is steadily increasing. However, information regarding the natural history of T1DM remains incomplete. The TrialNet Natural History Study of the Development of T1DM (Pathway to Prevention Study) has been designed to clarify this picture, and in so doing, will contribute to the development and implementation of studies aimed at prevention of and early treatment in T1DM. Purpose: TrialNet is an international network dedicated to the study, prevention, and early treatment of type 1 diabetes. TrialNet sites are located throughout the United States, Canada, Finland, United Kingdom, Italy, Germany, Sweden, Australia, and New Zealand. TrialNet is dedicated to testing new approaches to the prevention of and early intervention for type 1 diabetes. The goal of the TrialNet Natural History Study of the Development of Type 1 Diabetes is to enhance our understanding of the demographic, immunologic, and metabolic characteristics of individuals at risk for developing type 1 diabetes. The Natural History Study will screen relatives of people with type 1 diabetes to identify those at risk for developing the disease. Relatives of people with type 1 diabetes have about a 5% percent chance of being positive for the antibodies associated with diabetes. TrialNet will identify adults and children at risk for developing diabetes by testing for the presence of these antibodies in the blood. A positive antibody test is an early indication that damage to insulin-secreting cells may have begun. If this test is positive, additional testing will be offered to determine the likelihood that a person may develop diabetes. Individuals with antibodies will be offered the opportunity for further testing to determine their risk of developing diabetes over the next 5 years and to receive close monitoring for the development of diabetes.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Official eligibility criteria
Inclusion Criteria: * Individuals 2 to 45 years old who have an immediate family member with type 1 diabetes (such as a child, parent, or sibling) * Individuals 2-20 years old who have an extended family member with type 1 diabetes (such as a cousin, niece, nephew, aunt, uncle, grandparent, or half-sibling) * Those aged 2 years to 45 years who are not family members and are known to have 1 or more islet antibodies Exclusion Criteria: To be eligible a person must not: * Have diabetes already * Have previous or current use of medications for the control of hyperglycemia/diabetes. * Currently be using immunosuppressive or immunomodulatory agents (topical and inhaled agents are acceptable) * Have known severe active diseases, and/or diseases which are likely to limit life expectancy or lead to the use of chronic immunosuppressive or immunomodulatory therapies during the course of the study
Study sites (17)
CA
- Childrens Hospital of Orange County · Orange, CA 92868Marissa Erickson · Study contact · 714-509-8613 · merickson@choc.orgMark Daniels, MD · Principal investigatorMore trials in Orange
- University of California San Francisco · San Francisco, CA 94143-0434Karen Ko · Study contact · 844-813-8273 · clinicalresearch@diabetes.ucsf.eduStephen Gitelman, MD · Principal investigatorMore trials in San Francisco
- Stanford University Medical Center · Stanford, CA 94305-5208Trudy Esrey, RD · Study contact · 650-498-4450 · tesrey@stanford.eduDarrell Wilson, MD · Principal investigatorMore trials in Stanford
CO
- Barbara Davis Center for Childhood Diabetes · Denver, CO 80262Brenda Bradfield · Study contact · 303-724-8595 · brenda.bradfield@CUANSCHUTZ.EDUAndrea Steck, MD · Principal investigatorMore trials in Denver
CT
- Yale University School of Medicine · New Haven, CT 06519Lori Carria · Study contact · 203-737-3595 · lori.carria@yale.eduJennifer Sherr, MD · Principal investigatorMore trials in New Haven
FL
- University of Florida · Gainesville, FL 32601-0296Jennifer Hosford · Study contact · 352-294-5759 · jennifer.hosford@peds.ufl.eduMichael Haller, MD · Principal investigatorMore trials in Gainesville
GA
- Emory Children's Center · Atlanta, GA 30322Xiaomiao Lan-Pidhainy, RN · Study contact · 404-712-0051 · xlanpid@emory.eduAndrew Muir, MD · Principal investigatorMore trials in Atlanta
IN
- Riley Hospital for Children, Indiana University · Indianapolis, IN 46202Maria Spall · Study contact · 866-230-8486 · malnicho@iu.eduLinda DeMeglio, MD · Principal investigatorMore trials in Indianapolis
MA
- Joslin Diabetes Center · Boston, MA 02215Nora Bryant · Study contact · 617-309-4141 · nora.bryant@joslin.harvard.eduJason Gaglia, MD · Principal investigatorMore trials in Boston
MN
- University of Minnesota · Minneapolis, MN 58944Beth Pappenfus · Study contact · 612-624-2922 · papp0086@umn.eduAntoinette Moran, MD · Principal investigatorMore trials in Minneapolis
MO
- The Children's Mercy Hospital · Kansas City, MO 64111Cassandra McClain · Study contact · 816-960-8877 · clmcclain@cmh.eduWayne Moore, Md, PhD · Principal investigatorMore trials in Kansas City
NY
- Columbia University · New York, NY 10032Jamie R Hyatt · Study contact · 212-851-5425 · jh4470@cumc.columbia.eduRobin S Goland, MD · Principal investigatorMore trials in New York
PA
- Children's Hospital of Pittsburgh of UPMC · Pittsburgh, PA 15213Kelli DeLallo, RN · Study contact · 412-692-5210 · kelli.delallo@chp.eduDorothy Becker, MD · Principal investigatorMore trials in Pittsburgh
TN
- Vanderbilt University · Nashville, TN 37232Faith Brendle, RN · Study contact · 615-936-8638 · faith.brendle@vanderbilt.eduWilliam Russell, MD · Principal investigatorMore trials in Nashville
TX
- University of Texas Medical Center at Dallas · Dallas, TX 75390-8858Lindsay Harter · Study contact · 214-648-4725 · Lindsay.Harter@UTSouthwestern.eduPerrin White, MD · Principal investigatorMore trials in Dallas
- Baylor College of Medicine · Houston, TX 77030Sandra Pena · Study contact · 832-822-3380 · sypena@texaschildrens.orgMaria Redondo, MD · Principal investigatorMore trials in Houston
WA
- Benaroya Research Institute · Seattle, WA 98101-2795Katie Bennett · Study contact · 206-341-8945 · diabetes@benaroyaresearch.orgCarla Greenbaum, MD · Principal investigatorMore trials in Seattle