Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06658067

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Fair Haven Community Health Care (FHCHC)

New Haven, Connecticut, United States, 06520

Actively Recruiting

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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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