The T1D Exchange Registry
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 50,000
- 试验地点
- 1
- 主要终点
- Gather longitudinal data from individuals living with type 1 diabetes.
研究概览
简要总结
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
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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.
排除标准
- 未提供
结局指标
主要结局
Gather longitudinal data from individuals living with type 1 diabetes.
时间窗: 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.
次要结局
未报告次要终点
研究者
Kelsie LaFerriere
Lead Research Study Coordinator
T1D Exchange, United States