Actively Recruiting
Personalized Nutrition for Type 2 Diabetes
Led by University of Minnesota · Updated on 2025-07-15
72
Participants Needed
1
Research Sites
106 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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).
CONDITIONS
Official Title
Personalized Nutrition for Type 2 Diabetes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- At least 18 years of age
- Previous diagnosis of type 2 diabetes mellitus
- Hemoglobin A1c (HbA1c) level between 6.8% and 8.5%
You will not qualify if you...
- Diagnosis of type 1 diabetes mellitus
- Treatment with insulin, sulfonylurea, or meglitinide
- Use of non-diabetic medications affecting blood glucose control (e.g., corticosteroids)
- Body mass index (BMI) less than 25 kg/m2 or less than 23 kg/m2 for participants who identify as Asian
- Weight change greater than 5 pounds in the 3 months before study enrollment
- Estimated glomerular filtration rate less than 60 ml/minute/1.73 m2
- Pregnancy, plans to become pregnant soon, or breastfeeding
- Anemia affecting HbA1c measurement
- Changes to glucose-lowering medications, including dose changes, in the 3 months before enrollment
- Presence of any disease that would make following the study protocol difficult
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Minnesota
Minneapolis, Minnesota, United States, 55455
Actively Recruiting
Research Team
A
Anne Bantle
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
TREATMENT
Number of Arms
4
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