CGM Intervention in Teens and Young Adults With Type 1 Diabetes (T1D) (CITY)
Volunteers
Health Professionals
What is the purpose of this trial?
Adolescents and young adults with T1D and poor glycemic control (age 14-< 25 years, T1D duration >12 months, HbA1c 7.5-<11.0%, using an insulin pump or MDI)) will be randomly assigned to either CGM or BGM. Sample size will be 150. The primary outcome assessment will be HbA1c after 6 months. Secondary outcomes will include HbA1c, CGM metrics (control group will wear blinded CGM at 13 and 24 weeks), and quality of life measures. The randomized trial will be followed by a 6-month extension study during which the RCT control group will initiate CGM and the RCT CGM group will continue CGM
- Trial withJaeb Center for Health Research
- Ages14 years - 24 years
- GenderBoth
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Principal Investigator
- Last Updated04/21/2023
- Study HIC#2000021899