The T1D Exchange Registry

Recruiting now

Conditions studied: Diabetes Mellitus, Type 1, Diabetes, Type 1 Diabetes, Diabetes Mellitus

In brief

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

Key facts

Study ID

NCT04629586

Run by

T1D Exchange, United States

People needed

50000

Starts

2018-12-13

Expected to finish

2030-12-31

Last updated by the study team

2023-05-08

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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.

Where it is running

• T1D Exchange — Boston, Massachusetts, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.