Benefits of Continuous Glucose Monitoring With GEM Lifestyle Modification for Adults With Type 2 Diabetes
Primary Purpose
Diabetes Mellitus, Type 2
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
GEM lifestyle modification & continuous glucose monitoring
Routine Care
Sponsored by

About this trial
This is an interventional treatment trial for Diabetes Mellitus, Type 2
Eligibility Criteria
Inclusion Criteria:
- Type 2 diabetes
- Between the ages of 21 and 80
- Failed on an oral medication regimen (HbA1c > 7.5%).
Exclusion Criteria:
- Takes insulin
- Took medications in the last 3 months that impede weight loss (e.g., prednisone)
- Pregnant or contemplating pregnancy in the next 12 months
- Conditions that preclude increasing physical activity (e.g. severe neuropathy, cardiovascular disease, chronic obstructive pulmonary disease/emphysema, osteoarthritis, stroke)
- Severe mental disease (e.g. manic depressive illness, severe depression, or active substance abuse)
- Undergoing treatment for cancer
- History of lactic acidosis
- Marked renal impairment (eGFR < 45; stage 3b chronic kidney disease)
- Takes psychotropic medications that raise blood glucose (e.g. atypical antipsychotics)
- Cannot read English.
Sites / Locations
- University of Virginia, Dept. of Psychiatry and Neurobehavioral Sciences
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
GEM+CGM
Routine Care
Arm Description
GEM lifestyle modification & continuous glucose monitoring
Subject's current t2d treatment
Outcomes
Primary Outcome Measures
HbA1c
Change in HbA1c measured via blood test
Medication changes
Changes in prescribed medications (type and/or dosage)
Secondary Outcome Measures
change in food choices (ASA24 survey)
ASA24 survey across 3 separate days
change in food choices (energy bar selection)
At assessment visits, subjects will choose between energy bars that do or dont support the intervention principles.
Exercise (Fitbit)
daily activity will be recorded
change in psychological functioning (dietary habits questionnaire)
The Food Questionnaire
change in psychological functioning (quality of life questionnaire)
WHOQO-BREF Questionnaire
change in psychological functioning (depression questionnaire)
Patient Health Questionnaire (PHQ-9)
change in psychological functioning (numeracy questionnaire)
Numeracy Scale - measures how good one is with numbers
change in psychological functioning (diabetes knowledge questionnaire)
Diabetes Knowledge Scale - measures diabetes knowledge
change in psychological functioning (empowerment questionnaire)
Diabetes Empowerment Scale
Psychological functioning (PAID questionnaire)
Problem Area In Diabetes scale (PAID) - measures concerns about diabetes
change in psychological functioning (attitude towards glucose monitoring questionnaire)
The Glucose Monitoring Satisfaction Survey (GMSS)
Full Information
NCT ID
NCT03207893
First Posted
October 28, 2016
Last Updated
February 24, 2021
Sponsor
University of Virginia
Collaborators
DexCom, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT03207893
Brief Title
Benefits of Continuous Glucose Monitoring With GEM Lifestyle Modification for Adults With Type 2 Diabetes
Official Title
Benefits of Adding Continuous Glucose Monitoring to Glycemic Load, Exercise, and Monitoring of Blood Glucose (GEM) for Adults With Type 2 Diabetes - Phase 2
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
July 19, 2018 (Actual)
Primary Completion Date
January 23, 2020 (Actual)
Study Completion Date
January 23, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia
Collaborators
DexCom, Inc.
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
The purpose of this study is to determine if the use of continuous glucose monitoring with the GEM lifestyle modification program (Glycemic load, Exercise and Monitoring glucose) will result in better diabetes control than routine care.
Detailed Description
Type 2 diabetes (t2d) is a major epidemic of the developing world which has huge fiscal consequences and many physical complications. It is thought to be brought on in part by contemporary easy access to high energy foods and reduced physical activity, resulting in increased belly fat that culminates in growing insulin resistance and subsequent hyperglycemia. Because of ease and efficacy of medication management, t2d is primarily managed with ever-escalating medication use, which significantly contributes to medical cost and possibly the progression of the disease itself.
An effective supplement or alternative to medication management is lifestyle modification. Conventional lifestyle modification focuses on reducing body fat and insulin resistance through weight reduction from caloric restriction and aerobic exercise. Sustained routine application of this approach is limited because some individuals do not need to lose weight, some do not want to lose weight, others cannot lose weight, and when successful, lifelong weight reduction is difficult to sustain. A useful paradigm shift in lifestyle treatment of t2d might be to go from reducing calories to reducing postprandial glucose (PPG), the primary contributor to glycosylated hemoglobin (HbA1c).
PPG spikes can be prevented by replacing high with low glycemic load foods and dampened by engaging in postprandial physical activity. This is exemplified by the integrated Glycemic load, Exercise and Monitoring glucose (GEM) program. It promotes choices of low glycemic load foods and increased physical activity, directed by glucose monitoring feedback. Glucose feedback can: 1) educate people as to what food choices minimize PPG and what physical activity choices directly lower PPG, 2) activate individuals when glucose is out of their desired range by alerting them to make choices to lower high glucose or raise low glucose, and 3) motivate individuals to repeat those choices that resulted in desirable glucose consequences. The educating, activating and motivating benefits of glucose feedback are thought to be qualitatively and quantitatively enhanced through continuous glucose monitoring (CGM).
It is hypothesized that, compared to Routine Care (RC), GEM with CGM (GEM+CGM) administered to adults with t2d who are failing with oral medication management will result in better diabetes control (lower HbA1c), reduced medication management (less medication), and better psychological functioning (e.g. greater sense of empowerment) in the short term (3 month follow-up). Further, it is hypothesized that their reduction in HbA1c will be driven by a reduction in PPG.
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
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
24 (Actual)
8. Arms, Groups, and Interventions
Arm Title
GEM+CGM
Arm Type
Experimental
Arm Description
GEM lifestyle modification & continuous glucose monitoring
Arm Title
Routine Care
Arm Type
Active Comparator
Arm Description
Subject's current t2d treatment
Intervention Type
Behavioral
Intervention Name(s)
GEM lifestyle modification & continuous glucose monitoring
Intervention Description
Four treatment sessions of GEM lifestyle modification in 3 months and continuous glucose monitoring during the first 14 days of each of the 3 months.
Intervention Type
Other
Intervention Name(s)
Routine Care
Intervention Description
Subject's current t2d treatment
Primary Outcome Measure Information:
Title
HbA1c
Description
Change in HbA1c measured via blood test
Time Frame
baseline, 3 months post-intervention
Title
Medication changes
Description
Changes in prescribed medications (type and/or dosage)
Time Frame
baseline, 3 months post-intervention
Secondary Outcome Measure Information:
Title
change in food choices (ASA24 survey)
Description
ASA24 survey across 3 separate days
Time Frame
baseline, 3 months post-intervention
Title
change in food choices (energy bar selection)
Description
At assessment visits, subjects will choose between energy bars that do or dont support the intervention principles.
Time Frame
baseline, 3 months post-intervention
Title
Exercise (Fitbit)
Description
daily activity will be recorded
Time Frame
baseline, 3 months post-intervention
Title
change in psychological functioning (dietary habits questionnaire)
Description
The Food Questionnaire
Time Frame
baseline, 3 months post-intervention
Title
change in psychological functioning (quality of life questionnaire)
Description
WHOQO-BREF Questionnaire
Time Frame
baseline, 3 months post-intervention
Title
change in psychological functioning (depression questionnaire)
Description
Patient Health Questionnaire (PHQ-9)
Time Frame
baseline, 3 months post-intervention
Title
change in psychological functioning (numeracy questionnaire)
Description
Numeracy Scale - measures how good one is with numbers
Time Frame
baseline, 3 months post-intervention
Title
change in psychological functioning (diabetes knowledge questionnaire)
Description
Diabetes Knowledge Scale - measures diabetes knowledge
Time Frame
baseline, 3 months post-intervention
Title
change in psychological functioning (empowerment questionnaire)
Description
Diabetes Empowerment Scale
Time Frame
baseline, 3 months post-intervention
Title
Psychological functioning (PAID questionnaire)
Description
Problem Area In Diabetes scale (PAID) - measures concerns about diabetes
Time Frame
baseline, 3 months post-intervention
Title
change in psychological functioning (attitude towards glucose monitoring questionnaire)
Description
The Glucose Monitoring Satisfaction Survey (GMSS)
Time Frame
baseline, 3 months post-intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Type 2 diabetes
Between the ages of 21 and 80
Failed on an oral medication regimen (HbA1c > 7.5%).
Exclusion Criteria:
Takes insulin
Took medications in the last 3 months that impede weight loss (e.g., prednisone)
Pregnant or contemplating pregnancy in the next 12 months
Conditions that preclude increasing physical activity (e.g. severe neuropathy, cardiovascular disease, chronic obstructive pulmonary disease/emphysema, osteoarthritis, stroke)
Severe mental disease (e.g. manic depressive illness, severe depression, or active substance abuse)
Undergoing treatment for cancer
History of lactic acidosis
Marked renal impairment (eGFR < 45; stage 3b chronic kidney disease)
Takes psychotropic medications that raise blood glucose (e.g. atypical antipsychotics)
Cannot read English.
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
University of Virginia, Dept. of Psychiatry and Neurobehavioral Sciences
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Links:
URL
http://www.diabetes.org/living-with-diabetes/complications/
Description
American Diabetes Association (2012). Living with diabetes: Complications. Retrieved on 5/17/15
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Benefits of Continuous Glucose Monitoring With GEM Lifestyle Modification for Adults With Type 2 Diabetes
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