Home › Type 2 Diabetes › NCT06784375

Individualized Diabetes Education Assisted by CGM (IDEA-CGM)

Who can join

Ages 18 and older · All sexes

Inclusion Criteria:

* at least 18 years of age
* previous diagnosis of T2DM
* HbA1c of 6.8-8.5%

Exclusion Criteria:

* 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."

About the study

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).

What is being tested

• Unblinded CGM/Nutrition Therapy (behavioral)
• Blinded CGM/Nutrition Therapy (behavioral)
• Unblinded CGM/No Nutrition Therapy (behavioral)
• Blinded CGM/No Nutrition Therapy (behavioral)

Sponsor: University of Minnesota · Participants: 72 · Started: Jul 14, 2025

Contact the study team

• Anne Bantle · Phone: 612-625-8673

Official record on ClinicalTrials.gov — NCT06784375

Locations in the U.S.

Conditions

• Type 2 Diabetes

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.