Skip to main content
OpenTrials
Completed

NCT Number: NCT07587151

Remote Pharmacy Services Plus Continuous Glucose Monitoring in an Underserved Population

The purpose of this study is to improve T2DM (type 2 diabetes mellitus) management and health outcomes among underserved patients who receive primary care at a federally qualified health center (FQHC) in Winnebago County, Illinois.

Our aim is to assess the feasibility and preliminary effectiveness of a pilot program combining continuous glucose monitoring (CGM) with monthly telehealth appointments to improve diabetes management in FQHC patients who have uncontrolled T2DM (HbA1c >7%).

Researchers will compare those who receive the intervention (usual in-person care + CGM + 2 telehealth visits with a clinical pharmacist and family medicine resident) with those receiving a CGM in additional to usual care (in-person care + CGM).

Participants will have their HbA1c tested and complete surveys to assess diabetes-related distress and diabetes management self-efficacy at baseline and 3 and 6 months from baseline. This will allow the investigators to raise glucose awareness for all participants utilizing CGM technology while simultaneously determining the necessity of more frequent follow-up than the guideline recommended intervals of 3 months for uncontrolled diabetes in an under-resourced population. This will also allow us to evaluate the feasibility of telehealth in delivering more frequent follow-up care to patients with T2DM.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Illinois College of Medicine Rockford

Rockford, Illinois, 61107, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient receiving primary care from the study clinical site
  • Uncontrolled T2DM (HbA1c >7%)
  • 18 years of age and older

Exclusion criteria

  • Patients younger than 18 years of age
  • Patients in correctional facilities
  • Pregnant or lactating women
  • Current Continuous Glucose Monitoring device (CGM) users
  • Patients with gestational diabetes mellitus or Type 1 diabetes mellitus

Treatment and study plan

CGM plus telehealth

Other

Participants will receive CGM supplies for 3 months plus 2 monthly telehealth appointments.

CGM only

Other

Participants will receive CGM supplies for 3 months

Primary outcomes

  1. HbA1c

    Time frame: Enrollment, 3 months, and 6 months

    Hemoglobin A1c

Secondary outcomes

  1. Diabetes-related distress

    Time frame: Enrollment, 3 months, and 6 months

    Diabetes-related distress as assessed by the TYPE 2 DIABETES DISTRESS ASSESSMENT SYSTEM (T2-DDAS)

  2. Diabetes Management Self-Efficacy

    Time frame: Baseline, 3 months, and 6 months

    Diabetes management self-efficacy as assessed by the Stanford English Diabetes Self-Management study diabetes self-efficacy questionnaire.

    Stanford English Diabetes Self-Management study. Study reported in Lorig K, Ritter PL, Villa FJ, Armas J. Community-Based Peer-Led Diabetes Self-Management: A Randomized Trial. The Diabetes Educator 2009; Jul-Aug;35(4):641-51.

Sponsors and collaborators

Lead sponsor

University of Illinois at Chicago

Other

Registry information

Official study title

The Role of Remote Pharmacy Services With Continuous Glucose Monitoring in an Underserved Population

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
May 14, 2026
Registry last updated
May 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.