The T1D Exchange Registry
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: No intervention.
- Who it may be relevant to
- Registry conditions: Diabetes Mellitus, Type 1, Diabetes, Type 1 Diabetes, Diabetes Mellitus. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
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
Interventions
- Other No intervention
Observational research study
Primary outcome measures
- Gather longitudinal data from individuals living with type 1 diabetes. [Time frame: 10 years]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
United States · 1 center
- T1D Exchange — Boston
Identifiers
NCT: NCT04629586 · 1822333