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Recruiting

NCT Number: NCT04629586

The T1D Exchange Registry

The T1D Exchange Registry is a research study, conducted over time, for individuals with type 1 diabetes and their supporters. Participants volunteer to provide their data for research (for example, by answering questions in annual surveys). Once enrolled, Registry participants have the opportunity to sign up for other studies on various topics related to type 1 diabetes.

To participate, you will be asked to:

* Read and sign an online informed consent form * Take a survey describing specific demographic and type 1 diabetes management information * Update your information annually * Periodically opt in for additional research opportunities (if you choose), i.e. taking new surveys or uploading health device data

Recruiting

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Key information

Conditions

Diabetes Mellitus, Type 1 Autoimmune Diseases Diabetes Diabetes Mellitus Endocrine System Diseases Glucose Metabolism Disorders Hyperinsulinism Immune System Diseases Insulin Resistance Metabolic Diseases Nutritional and Metabolic Diseases Type 1 Diabetes

Sex eligibility

All sexes

Study type

Observational

Primary location

T1D Exchange

Boston, Massachusetts, 02111, United States

Location status: Recruiting

Location contact

Kelsie LaFerriere

CONTACT

[email protected]

617-892-9941

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical diagnosis of type 1 diabetes.
  • Individuals younger than 18 years of age must have parent/guardian consent.
  • Must be able to read and understand English.
  • Currently living in the United States

Exclusion criteria

  • Does not use insulin and has not had a pancreatic or islet cell transplant.
  • Cannot fully read and understand English.
  • Does not currently live in the United States.

Treatment and study plan

No intervention

Other

Observational research study

Primary outcomes

  1. Gather longitudinal data from individuals living with type 1 diabetes.

    Time frame: 10 years

    Gather longitudinal data on disease, health status, and patient-reported outcomes of individuals living with type 1 diabetes. This will be achieved by presenting participants with annual questionnaires, tracking any changes in their responses over time.

Study contacts

Contact information is provided by the study sponsor or research team.

Julia Ravelson

CONTACT

[email protected]

(617) 892-9941

Kelsie LaFerrier

CONTACT

[email protected]

(617) 892-9941

Sponsors and collaborators

Lead sponsor

T1D Exchange, United States

Other

Registry information

Acronym: T1D Registry

Important dates

Study start
2018
Primary completion
2030
Study completion
2030
First posted
Nov 16, 2020
Registry last updated
May 8, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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