Actively Recruiting
Continuous Glucose Monitors (CGMs) for All: Studying the Impact of Expanding CGM Access
Led by Yale University · Updated on 2025-12-03
17
Participants Needed
1
Research Sites
80 weeks
Total Duration
On this page
Sponsors
Y
Yale University
Lead Sponsor
Y
Yale Office of Global Health
Collaborating Sponsor
AI-Summary
What this Trial Is About
This non-blinded, non-randomized pre-post study will examine the impact of providing CGM sensors free of charge to adult patients of Fair Haven Community Health Care with poorly controlled type 2 diabetes on glycemic control and quality of life.
CONDITIONS
Official Title
Continuous Glucose Monitors (CGMs) for All: Studying the Impact of Expanding CGM Access
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed and dated informed consent form
- Willingness to comply with all study procedures and be available for the study duration
- Diagnosed with type 2 diabetes mellitus
- A1c of 8.0 or greater within two weeks before enrollment
- Using insulin for at least one year, with or without other diabetes medications
- Able and willing to wear CGM sensors for 14-day periods during the trial
- Able and willing to follow provider-directed medication adjustments
- Unable to afford CGM sensors
You will not qualify if you...
- Not currently using insulin (insulin naive)
- Experienced diabetic ketoacidosis in the past 6 months
- Has end-stage renal disease
- Has medical reasons preventing use of CGM
- Has active insurance that sufficiently covers CGM sensor costs
- Currently pregnant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Fair Haven Community Health Care (FHCHC)
New Haven, Connecticut, United States, 06520
Actively Recruiting
Research Team
J
Justin A Dower, MD
CONTACT
A
Anne Camp, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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