RECRUITING

Pharmacist-led Continuous Glucose Monitoring

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a pilot study. The goal of this prospective cohort study is to determine impact of pharmacist-led continuous glucose monitoring on glycemic control and health behavior change in people with type 2 diabetes. The main questions it aims to answer are: 1. to assess change in hemoglobin A1c in people with type 2 diabetes using continuous glucose monitoring under a pharmacist-led approach as compared to a pharmacist-led approach utilizing no continuous glucose monitoring (only self-monitoring blood glucose with a glucometer). 2. to assess change in continuous glucose monitoring-derived glycemic outcomes among the pharmacist-led continuous glucose monitoring cohort (intervention group) 3. to assess change in health behavior among the pharmacist-led continuous glucose monitoring cohort (intervention group)

Official Title

Investigating the Impact of Pharmacist-led Flash Continuous Glucose Monitoring on Clinical and Behavioral Health Outcomes

Quick Facts

Study Start:2024-09-01
Study Completion:2025-08-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06572306

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * type 2 diabetes
  2. * hemoglobin A1c ≥ 8%
  3. * compatible smartphone with FreeStyle Libre 2 continuous glucose monitoring system
  4. * current use and access to a glucometer for self-monitoring of blood glucose
  1. * any continuous glucose monitor use within 6 months prior to study enrollment
  2. * pregnant and planning to become pregnant during study time frame
  3. * history of hypoglycemia requiring third party assistance
  4. * history of diabetic ketoacidosis or hyperosmolar hyperglycemic state within 6 months prior to study enrollment
  5. * known allergy to medical grade adhesives
  6. * current use of systemic steroids for any medical condition
  7. * current use of dialysis

Contacts and Locations

Study Contact

Kevin Cowart, PharmD, MPH
CONTACT
813-974-5562
kcowart2@usf.edu

Principal Investigator

Kevin Cowart, PharmD, MPH
PRINCIPAL_INVESTIGATOR
University of South Florida

Study Locations (Sites)

USF Health Department of Family Medicine - Morsani Center for Advanced Health Care
Tampa, Florida, 33612
United States
USF Health Department of Family Medicine - University Partnership Center
Tampa, Florida, 33613
United States

Collaborators and Investigators

Sponsor: University of South Florida

  • Kevin Cowart, PharmD, MPH, PRINCIPAL_INVESTIGATOR, University of South Florida

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-09-01
Study Completion Date2025-08-05

Study Record Updates

Study Start Date2024-09-01
Study Completion Date2025-08-05

Terms related to this study

Keywords Provided by Researchers

  • type 2 diabetes
  • endocrine disorders
  • continuous glucose monitor
  • pharmacist

Additional Relevant MeSH Terms

  • Type 2 Diabetes