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The Use of Libre to Improve Metabolic Control and Reduce Reliance on Medication

Primary Purpose

Diabetes Mellitus, Type 2

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
GEM + CGM
Sponsored by
University of Virginia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2

Eligibility Criteria

35 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:(GEM group)

  1. Provision of signed and dated informed consent form.
  2. Willing to comply with study procedures and be available for the entire study.
  3. 35 to 85 years of age, inclusive.
  4. Diagnosed with Type 2 Diabetes within the last 12 months.
  5. HbA1c between 6.5% and 11.5%.
  6. Medical record contains HbA1c, lipid panel, BMI and blood pressure measures collected in the past three months.

Inclusion Criteria:(Routine Care group)

  1. 35 to 85 years of age, inclusive.
  2. Diagnosed with Type 2 Diabetes within the last 12 months.
  3. HbA1c between 6.5% and 11.5%.
  4. Medical record contains HbA1c, lipid panel, BMI and blood pressure measures collected in the past three months.

Exclusion Criteria (GEM group):

  1. Has Type 1 Diabetes
  2. Currently takes diabetes medication
  3. Currently takes medication that can interfere with metabolic control, such as prednisone
  4. Has a condition that precludes a low carbohydrate diet, such as gastroparesis
  5. Has a physical or medical condition that precludes walking 120 steps per minute, for 10 minutes or longer
  6. Has kidney disease.
  7. Is receiving cancer treatment
  8. Cannot speak English
  9. Has blindness
  10. Is pregnant or anticipates becoming pregnant in the next 4 months
  11. Anticipates moving away within the next 4 months

Exclusion Criteria (Routine Care group): Individuals who met any of the following criteria in the first year after their T2D diagnosis will be excluded from the Routine Care group

  1. Took medication that can interfere with metabolic control, such as prednisone
  2. Had a condition that precludes a low carbohydrate diet, such as gastroparesis
  3. Had a physical or medical condition that precludes walking 120 steps per minute, for 10 minutes or longer
  4. Had kidney disease.
  5. Was receiving cancer treatment
  6. Was pregnant

Sites / Locations

  • Dept. of Psychiatry and Neurobehavioral Sciences, University of Virginia

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

GEM + CGM

Arm Description

A self-directed lifestyle intervention for controlling Type 2 Diabetes

Outcomes

Primary Outcome Measures

Total Treatment Effect (TTE)
Measures the effect of the intervention on HbA1c. The TTE factors out the confounding effects of diabetes medications on HbA1c by adjusting for each medication's HbA1c-lowering equivalent.

Secondary Outcome Measures

Blood glucose
CGM measurement of blood glucose time in range, time above 150 mg/dL and time above 180 mg/dL Higher time in range means better outcomes.Higher time above 150 and 180 mg/dL means worse outcomes.
Physical activity
FitBit measurement of hours active, active minutes, and total steps. Higher activity means better outcomes.
Food Choice Questionnaire: High Glycemic Load (HGL)
Measures the servings of HGL foods eaten in a typical week. The scale ranges from 0 to no maximum. Higher scores mean worse outcomes.
Food Choice Questionnaire: Low Glycemic Load (LGL)
Measures the servings of LGL foods eaten in a typical week. The scale ranges from 0 to no maximum. Higher scores mean better outcomes.
Patient Health Questionnaire (PHQ-8)
Measures depressive symptoms. The scale ranges from 0 to 24. Higher scores mean worse outcomes.
Diabetes Knowledge Scale
Measures diabetes-related knowledge. The scale ranges from 0 to 26. Higher scores mean better outcomes.
Diabetes Empowerment Scale
Measures the psychosocial self-efficacy of people with diabetes. The scale ranges from 0 to 40. Higher scores mean better outcomes.
Diabetes Distress Scale (Emotional Distress & Regimen Distress subscales)
Measures concerns about diabetes. Each subscale ranges from 5 to 30. Higher scores mean worse outcomes.
Treatment Optimization Scale
Generates user feedback about improving the intervention. The scale ranges from 43 to 215. Higher scores mean better outcomes.

Full Information

First Posted
November 3, 2020
Last Updated
October 4, 2021
Sponsor
University of Virginia
Collaborators
University of Colorado, Denver, West Virginia University
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1. Study Identification

Unique Protocol Identification Number
NCT04632849
Brief Title
The Use of Libre to Improve Metabolic Control and Reduce Reliance on Medication
Official Title
The Use of Libre to Educate, Motivate and Activate Adults With Newly Diagnosed Type 2 Diabetes to Improve Metabolic Control and Reduce Their Reliance on Medication: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
November 1, 2020 (Actual)
Primary Completion Date
August 1, 2021 (Actual)
Study Completion Date
September 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia
Collaborators
University of Colorado, Denver, West Virginia University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
GEM (Glycemic Excursion Minimization) is a new lifestyle treatment for type 2 diabetes that aims to lower glucose levels after meals and snacks. This is different from the current lifestyle treatment, which is to lose weight. This study is trying to find out if people who are newly diagnosed with type 2 diabetes can use a continuous glucose monitor together with the GEM lifestyle to improve control of their diabetes. Study participants will follow the GEM lifestyle for 4 months (1 month of treatment and 3 months of maintenance) instead of seeking usual care (medications or weight loss programs) to lower blood glucose.
Detailed Description
For people who are newly diagnosed with Type 2 Diabetes (T2D), it might be possible to delay or prevent the need for diabetic medications by reducing postprandial glucose (PPG). Our Glycemic Excursion Minimization (GEM) lifestyle intervention can reduce PPG, but it depends on blood glucose feedback to help the user learn what elevates their PPG. This study examines if continuous feedback from the Libre 2 continuous glucose monitor (CGM) will be advantageous for reaching the goals of GEM. We will recruit 18 adult participants newly diagnosed with type 2 diabetes who are interested in using the Libre 2 CGM. Six participants will be recruited from each of the primary care clinics at the University of Virginia (Dr. Cox), the University of Colorado (Dr. Oser) and the University of West Virginia, East Branch (Dr. Cucuzzella). Each site will also search their medical records to select 4 participants who match their study participants, meet the study criteria, but are being treated with routine care. These data will form the Routine Care control group (n=12). Routine Care participants will follow their doctor's treatment recommendations, while GEM participants will complete the 1-month, self-directed GEM lifestyle training using the Libre 2 CGM and a FitBit to monitor progress. They will then maintain the GEM lifestyle for 3 more months. The Total Treatment Effect (a measure of treatment effectiveness that considers both A1c and medication changes) will be calculated pre- and post-treatment from medical record data. CGM data from GEM participants will be collected and analyzed. CGM sensor use will be tracked to estimate participant engagement. We anticipate this multi-center pilot project will demonstrate the benefits of using Libre 2 with a structured lifestyle intervention designed to reduce postprandial blood glucose excursions for individuals newly diagnosed with T2D.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All participants will receive the GEM intervention.
Masking
None (Open Label)
Allocation
N/A
Enrollment
17 (Actual)

8. Arms, Groups, and Interventions

Arm Title
GEM + CGM
Arm Type
Experimental
Arm Description
A self-directed lifestyle intervention for controlling Type 2 Diabetes
Intervention Type
Behavioral
Intervention Name(s)
GEM + CGM
Intervention Description
Participants follow the GEM guidebook for 4 months (1 month of intervention and 3 months of maintenance) while wearing a FitBit activity monitor and a Freestyle Libre 2 CGM to provide feedback about activity and blood glucose. The GEM guidebook covers Routine choices, Recovering from blood glucose excursions, Reducing blood glucose excursions, and Maintenance.
Primary Outcome Measure Information:
Title
Total Treatment Effect (TTE)
Description
Measures the effect of the intervention on HbA1c. The TTE factors out the confounding effects of diabetes medications on HbA1c by adjusting for each medication's HbA1c-lowering equivalent.
Time Frame
Change from baseline TTE at 3 months post-intervention
Secondary Outcome Measure Information:
Title
Blood glucose
Description
CGM measurement of blood glucose time in range, time above 150 mg/dL and time above 180 mg/dL Higher time in range means better outcomes.Higher time above 150 and 180 mg/dL means worse outcomes.
Time Frame
Change from baseline blood glucose at 3 months post-intervention
Title
Physical activity
Description
FitBit measurement of hours active, active minutes, and total steps. Higher activity means better outcomes.
Time Frame
Change from baseline physical activity at 3 months post-intervention
Title
Food Choice Questionnaire: High Glycemic Load (HGL)
Description
Measures the servings of HGL foods eaten in a typical week. The scale ranges from 0 to no maximum. Higher scores mean worse outcomes.
Time Frame
Change from baseline Food Choice Questionnaire HGL at 3 months post-intervention
Title
Food Choice Questionnaire: Low Glycemic Load (LGL)
Description
Measures the servings of LGL foods eaten in a typical week. The scale ranges from 0 to no maximum. Higher scores mean better outcomes.
Time Frame
Change from baseline Food Choice Questionnaire LGL at 3 months post-intervention
Title
Patient Health Questionnaire (PHQ-8)
Description
Measures depressive symptoms. The scale ranges from 0 to 24. Higher scores mean worse outcomes.
Time Frame
Change from baseline PHQ-8 at 3 months post-intervention
Title
Diabetes Knowledge Scale
Description
Measures diabetes-related knowledge. The scale ranges from 0 to 26. Higher scores mean better outcomes.
Time Frame
Change from baseline Diabetes Knowledge Scale at 3 months post-intervention
Title
Diabetes Empowerment Scale
Description
Measures the psychosocial self-efficacy of people with diabetes. The scale ranges from 0 to 40. Higher scores mean better outcomes.
Time Frame
Change from baseline Diabetes Empowerment Scale at 3 months post-intervention
Title
Diabetes Distress Scale (Emotional Distress & Regimen Distress subscales)
Description
Measures concerns about diabetes. Each subscale ranges from 5 to 30. Higher scores mean worse outcomes.
Time Frame
Change from baseline Diabetes Distress Scale at 3 months post-intervention
Title
Treatment Optimization Scale
Description
Generates user feedback about improving the intervention. The scale ranges from 43 to 215. Higher scores mean better outcomes.
Time Frame
Change from baseline Treatment Optimization Scale at 3 months post-intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:(GEM group) Provision of signed and dated informed consent form. Willing to comply with study procedures and be available for the entire study. 35 to 85 years of age, inclusive. Diagnosed with Type 2 Diabetes within the last 12 months. HbA1c between 6.5% and 11.5%. Medical record contains HbA1c, lipid panel, BMI and blood pressure measures collected in the past three months. Inclusion Criteria:(Routine Care group) 35 to 85 years of age, inclusive. Diagnosed with Type 2 Diabetes within the last 12 months. HbA1c between 6.5% and 11.5%. Medical record contains HbA1c, lipid panel, BMI and blood pressure measures collected in the past three months. Exclusion Criteria (GEM group): Has Type 1 Diabetes Currently takes diabetes medication Currently takes medication that can interfere with metabolic control, such as prednisone Has a condition that precludes a low carbohydrate diet, such as gastroparesis Has a physical or medical condition that precludes walking 120 steps per minute, for 10 minutes or longer Has kidney disease. Is receiving cancer treatment Cannot speak English Has blindness Is pregnant or anticipates becoming pregnant in the next 4 months Anticipates moving away within the next 4 months Exclusion Criteria (Routine Care group): Individuals who met any of the following criteria in the first year after their T2D diagnosis will be excluded from the Routine Care group Took medication that can interfere with metabolic control, such as prednisone Had a condition that precludes a low carbohydrate diet, such as gastroparesis Had a physical or medical condition that precludes walking 120 steps per minute, for 10 minutes or longer Had kidney disease. Was receiving cancer treatment Was pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel J Cox, PhD
Organizational Affiliation
University of Virginia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dept. of Psychiatry and Neurobehavioral Sciences, University of Virginia
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33094208
Citation
Cox DJ, Banton T, Moncrief M, Conaway M, Diamond A, McCall AL. Minimizing Glucose Excursions (GEM) With Continuous Glucose Monitoring in Type 2 Diabetes: A Randomized Clinical Trial. J Endocr Soc. 2020 Aug 18;4(11):bvaa118. doi: 10.1210/jendso/bvaa118. eCollection 2020 Nov 1. Erratum In: J Endocr Soc. 2020 Nov 06;4(12):bvaa174.
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The Use of Libre to Improve Metabolic Control and Reduce Reliance on Medication

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