Assessing Continuous Glucose Monitor Use in Underserved Primary Care Patients
NCT05766488 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50
Last updated 2025-09-30
Summary
Continuous glucose monitoring (CGM) has demonstrated improved outcomes in both type 1 and type 2 diabetes populations in comparison to traditional methods; however, these devices have not been well studied in underserved adult patients (e.g., low-income, uninsured) who may face additional barriers to monitoring. Furthermore, there is limited data exploring long-term (3- to 6- month) health care team-based management of these devices in the primary care setting. The purpose of this study is to further understand the benefits and barriers associated with CGM use in underserved populations with type 2 diabetes and improve their overall diabetes care.
Conditions
Interventions
- DEVICE
-
Continuous Glucose Monitor (CGM)
A Freestyle Libre 2 continuous glucose monitor (CGM) will be provided in the experimental arm of this study for 6 months.
- DEVICE
-
Self-monitoring Blood Glucose (SMBG)
A traditional glucometer device will be assigned in the active comparitor arm of this study for 6 months.
Sponsors & Collaborators
-
Great Plains IDeA-CTR
collaborator UNKNOWN -
University of Nebraska
lead OTHER
Principal Investigators
-
Drew C Prescott, PharmD · University of Nebraska
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 19 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-07-24
- Primary Completion
- 2026-07-31
- Completion
- 2026-07-31
- FDA Device
- Yes
Countries
- United States
Study Locations
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