The T1D Exchange Registry

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

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

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• 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

Locations
United States
Massachusetts
T1D Exchange
RECRUITING
Boston
Contact Information
Primary
Kelsie LaFerrier
klaferriere@t1dexchange.org
(617) 892-9941
Backup
Julia Ravelson
jravelson@t1dexchange.org
(617) 892-9941
Time Frame
Start Date: 2018-12-13
Estimated Completion Date: 2030-12-31
Participants
Target number of participants: 50000
Treatments
Individuals diagnosed with type 1 diabetes
T1D Exchange Registry is currently looking for participants:~* Of all ages, genders, races, and ethnic groups~* Living in the United States~* Diagnosed with type 1 diabetes~* Currently taking insulin or have had a pancreatic or islet cell transplant
Related Therapeutic Areas
Sponsors
Leads: T1D Exchange, United States

This content was sourced from clinicaltrials.gov