Status:
NOT_YET_RECRUITING
CGM-Enhanced DPP to Prevent Type 2 Diabetes in Adults With Prediabetes
Lead Sponsor:
State University of New York at Buffalo
Conditions:
PreDiabetes
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Prediabetes affects over one-third of adults in the United States, placing them at a higher risk for developing type 2 diabetes and heart disease, which can lead to serious health complications and in...
Detailed Description
CGM devices give individuals real-time information about their blood sugar levels, which can help them understand how their diet, exercise, and daily habits impact their health. By pairing CGM technol...
Eligibility Criteria
Inclusion
- adults aged 18 years or older,
- diagnosis of prediabetes, as defined by current clinical guidelines (HbA1c 5.7% to 6.4%, fasting plasma glucose 100-125 mg/dL, or 2-hour plasma glucose 140-199 mg/dL following a 75g oral glucose tolerance test),
- body mass index (BMI) of at least 24 kg/m² (or 22 kg/m² for Asian Americans),
- willingness to comply with all aspects of the study protocol, including attending coaching sessions and using CGM devices.
Exclusion
- Individuals will be excluded from the study if they
- have a diagnosis of type 1 or type 2 diabetes,
- are currently using CGMs or have medical contraindications to CGM use, such as severe skin allergies or implantable defibrillators, or
- are currently enrolled in another clinical trial for prediabetes. Additionally, using validated assessments, we will exclude participants with significant dementia, alcohol or drug abuse/dependency, active psychosis, or life expectancy less than 12 months as these conditions are likely to interfere with adherence to the intervention.
Key Trial Info
Start Date :
January 2 2026
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 2 2028
Estimated Enrollment :
214 Patients enrolled
Trial Details
Trial ID
NCT07140848
Start Date
January 2 2026
End Date
January 2 2028
Last Update
August 26 2025
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