Type 2 Diabetes Clinical Trial
Official title:
Assessing Continuous Glucose Monitor Use in Underserved Primary Care Patients
The goal of this clinical trial is to evaluate the perceived and experienced benefits and barriers of Continuous Glucose Monitor (CGM) use and identify outcomes associated with CGM use relative to usual care with self-monitoring of blood glucose in an underserved patient population with type 2 diabetes.
The goal of this clinical trial is to evaluate the perceived and experienced benefits and barriers of CGM use and identify outcomes associated with CGM use relative to usual care with self-monitoring of blood glucose in an underserved patient population with type 2 diabetes. The main questions it aims to answer are: - What are the perceived and experienced benefits of CGM use in an underserved patient population with type 2 diabetes? - What differences are there in glucose monitoring frequency and glucose control between CGM and traditional glucometer testing in an underserved patient population with type 2 diabetes? Participants will: - Complete a baseline and final survey evaluating perceived/expected benefits or barriers to CGM use - Be assigned to a CGM or usual care (traditional glucometer) arm for 6 months within an interprofessional primary care setting - Complete laboratory testing at regular intervals that don't differ from usual diabetes care Researchers will compare the CGM group to the traditional glucometer group to see if there are differences between (1) perceived/experienced benefits or barriers to the use of these devices, (2) glycemic clinical outcomes (hemoglobin A1c, hypoglycemia, hyperglycemia), and (3) glycemic measurement frequency. ;
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