PDF: Patient-Driven Lifestyle Modification Using FreeStyle Libre in Type 2 Diabetes Patients

Sponsor
Seoul National University Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04932928
Collaborator
Inje University (Other), Kangbuk Samsung Hospital (Other)
126
1
2
24
5.3

Study Details

Study Description

Brief Summary

We aim to provide medical nutritional therapy to patients with type 2 diabetes who are on oral hypoglycemic agents or on basal insulin only and monitor the glycemic response with flash glucose monitoring or self-monitoring of blood glucose.

Specifically, this is a randomized, open-label, controlled study where half of the study participants will have FreeStyle Libre device on for 12 weeks and compare the change in glycated hemoglobin (HbA1c) value with the patients in the control group.

Condition or Disease Intervention/Treatment Phase
  • Device: FreeStyle Libre
  • Device: Blood glucose meter
N/A

Detailed Description

Subjects: 126 patients with type 2 diabetes mellitus Scheme: Multi-center, Randomized, open-label, controlled study

This study is referred to as the "Patient-Driven lifestyle modification using FreeStyle Libre in type 2 diabetes patients", also known as the PDF study.

It will assess potential benefits of using Continuous Glucose Monitoring (CGM) versus Self Monitoring of Blood Glucose (SMBG) when combined with personalized education on lifestyle modification in people with type 2 diabetes. Specifically, we will investigate patients who have an elevated HbA1c between 7.0 - 10.0% who are not using prandial insulin.

Potential participants will be screened from routine outpatient clinic visits, will be randomized to either the CGM or SMBG group in a 1:1 ratio. Participants from both groups will receive education on lifestyle modification and will be reminded every 4 weeks with structured phone visits. Study will be completed at the visit on 12 weeks of follow up with the same laboratory examinations (including HbA1c) and survey from the baseline.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
126 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Patient-Driven Lifestyle Modification Using FreeStyle Libre in Type 2 Diabetes Patients
Actual Study Start Date :
Mar 23, 2021
Anticipated Primary Completion Date :
Sep 23, 2022
Anticipated Study Completion Date :
Mar 23, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: FreeStyle Libre (CGM) Group

Device: FreeStyle Libre (ver 1.0) Education on lifestyle modification

Device: FreeStyle Libre
Flash glucose monitoring + Education on lifestyle modification
Other Names:
  • Education on lifestyle modification
  • Active Comparator: Self Monitoring of Blood Glucose (SMBG) Group

    Device: Blood glucose meter Education on lifestyle modification

    Device: Blood glucose meter
    Self monitoring of blood glucose + Education on lifestyle modification
    Other Names:
  • Education on lifestyle modification
  • Outcome Measures

    Primary Outcome Measures

    1. Change in HbA1c [Baseline to Month 3]

      Between group differences (CGM and SMBG) for the change in HbA1c from baseline to Month 3

    Secondary Outcome Measures

    1. Change in mean fasting glucose [Baseline to Month 3]

      Between group differences (CGM and SMBG) for the change in fasting glucose from baseline to Month 3

    2. Change in body weight [Baseline to Month 3]

      Between group differences (CGM and SMBG) for the change in body weight from baseline to Month 3

    3. Change in blood pressure [Baseline to Month 3]

      Between group differences (CGM and SMBG) for the change in blood pressure from baseline to Month 3

    4. Change in waist circumference [Baseline to Month 3]

      Between group differences (CGM and SMBG) for the change in waist circumference from baseline to Month 3

    5. Change in lipid level [Baseline to Month 3]

      Between group differences (CGM and SMBG) for the change in lipid level (total cholesterol, triglycerides, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol) from baseline to Month 3

    6. Change in the Korean Version of Revised Summary of Diabetes Self-Care Activities Questionnaire (SDSCA-K) survey score [Baseline to Month 3]

      Between group differences (CGM and SMBG) for the change in survey score from baseline to Month 3

    Other Outcome Measures

    1. Change in CGM time in target range [Baseline to Month 3]

      Change in CGM time in target range 70-180 mg/dL from baseline to Month 3 in the CGM group

    2. Change in CGM time-hyperglycemic [Baseline to Month 3]

      Change in CGM time in time above target range, defined as >250 mg/dL from baseline to Month 3 in the CGM group

    3. Change in CGM time-hypoglycemic [Baseline to Month 3]

      Change in CGM time in time below target range, defined as <70 mg/dL (level 1) and < 54 (level 2) from baseline to Month 3 in the CGM group

    4. Change in CGM glucose variability [Baseline to Month 3]

      Change in CGM glucose variability measured by the coefficient of variation from baseline to Month 3 in the CGM group

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age 19-80

    • Diagnosed with type 2 diabetes mellitus (DM)

    • Uncontrolled type 2 DM: HbA1c 7.0-10.0%

    • Signed informed consent

    Exclusion Criteria:
    • Diagnosed with other types of diabetes mellitus (i.e. Type 1 DM)

    • Use of prandial insulin

    • Change in diabetes medication in the preceding 3 months

    • Pregnant/lactating women

    • Addiction to drugs and alcohol

    • Use of medications that result in drug-induced hyperglycemia (i.e. steroid)

    • Severe liver disease

    • End-stage renal disease (i.e. on dialysis)

    • Unable to wear CGM devices due to dermatologic side effects (i.e. severe burn, inflammation, active skin infection, severe skin reactions, hypertrichosis, etc.)

    • Conditions that impact the stability of HbA1c measurement

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Seoul National University Hospital Seoul Korea, Republic of 110-744

    Sponsors and Collaborators

    • Seoul National University Hospital
    • Inje University
    • Kangbuk Samsung Hospital

    Investigators

    • Principal Investigator: Young Min Cho, MD, PhD, Seoul National University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Seoul National University Hospital
    ClinicalTrials.gov Identifier:
    NCT04932928
    Other Study ID Numbers:
    • H-2011-062-117
    First Posted:
    Jun 21, 2021
    Last Update Posted:
    Jun 21, 2021
    Last Verified:
    Mar 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 21, 2021