Individualized Diabetes Education Assisted by CGM (IDEA-CGM)
Recruiting now · Not applicable
Conditions studied: Type 2 Diabetes
In brief
This project will compare medical nutrition therapy personalized by continuous glucose monitor (CGM) feedback to control interventions in participants with type 2 diabetes mellitus (T2DM).
Key facts
- Study ID
- NCT06784375
- Run by
- University of Minnesota
- People needed
- 72
- Starts
- 2025-07-14
- Expected to finish
- 2027-09-15
- Last updated by the study team
- 2026-07-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- at least 18 years of age
- previous diagnosis of T2DM
- HbA1c of 6.8-8.5%
You may not qualify if…
- type 1 diabetes mellitus
- treatment with insulin, sulfonylurea, or meglitinide
- use of nondiabetic medications that affect blood glucose control (such as corticosteroids)
- BMI <25 kg/m2 or <23 kg/m2 for participants who self-identify as Asian
- weight change >5 pounds in the 3 months prior to study enrollment
- estimated glomerular filtration rate <60 ml/minute/1.73 m2
- pregnancy or immediate plans to become pregnant 8) breastfeeding 9) anemia (which would affect measurement of HbA1c) 10) changes to glucose lowering medications, including change in dose, in the 3 months prior to enrollment 11) presence of any disease that would make adherence to the protocol difficult."
Where it is running
- University of Minnesota — Minneapolis, Minnesota, United States (enrolling)
Full record on ClinicalTrials.gov
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