IMPEDE: CGM Plus GEM in Prediabetes
Study Details
Study Description
Brief Summary
This study is designed to look into the effect of a lifestyle management guide called GEM (Glycemic Excursion Minimization) alongside continuous glucose monitoring (CGM) and an activity monitor (FitBit) and the effect this can have on persons with prediabetes.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Detailed Description
For people with prediabetes, it may be possible to delay or prevent the progression to diabetes by reducing postprandial glucose (PPG). The Glycemic Excursion Minimization (GEM) lifestyle intervention guide can reduce PPG in people with type 2 diabetes and has been studied in this population with continuous glucose monitor (CGM) feedback to help the user learn what elevates and lowers their PPG. This study examines if the GEM lifestyle intervention guide plus continuous feedback from the FreeStyle Libre 2 CGM and FitBit will allow participants with prediabetes with HbA1c 6.0-6.4% to (1) improve their metabolic status by illustrating the effects of their routine food and physical activity choices on their glucose levels and variability, more than Routine Care (RC), and (2) to enhance these investigations by adding comprehensive plasma proteomics to the analyses. The investigators will recruit up to 36 adult participants with prediabetes through the University of Colorado, with the goal of having at least 30 participants complete the study. Participants will be randomized to the intervention or RC. Those randomized to the intervention will be given a GEM treatment manual, Libre2 CGM, and an activity monitor and will follow the GEM lifestyle intervention guide for 4 months. Those participants randomized to RC will follow recommendations from their primary care provider. RC participants will have the opportunity to receive GEM four months after consenting and completing the RC pre-post assessments if they meet eligibility criteria. It is anticipated that 50% of the RC participants will want/be able to cross over to GEM upon completion of RC. Pre-post blinded CGM data and activity data, clinical, and psychosocial outcomes will be collected and analyzed. It is anticipated that this pilot project will demonstrate the benefits of using GEM plus FreeStyle Libre 2 and FitBit to reduce percentage of CGM readings >120 mg/dL, from blinded pre-post FreeStyle Libre Pro, as well as reduce BMI and depressive symptoms and increase modified diabetes empowerment. Comprehensive proteomics will be measured on small samples of EDTA treated venous blood. Individual proteins and protein pathways will be measured for each of the participants.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: GEM + CGM + Activity Monitor GEM plus CGM and Activity Monitor (FitBit) |
Behavioral: GEM
The intervention group will be given Libre 2 supplies for 4 months, an activity monitor, and the 4-chapter GEM paper guide. The intervention group will complete a virtual or inperson study visit where they will receive instructions on how to apply their unblinded Freestyle Libre and connect it to the study account, as well as how to register their Fitbit to the study account. Participants will receive one telephone call to review use of the GEM Guide and call at two weeks and six weeks later when the probability of dropouts from lifestyle intervention peaks. Participants will follow the self-directed GEM guide for 4 months (a 1-month treatment period followed by a 3-month maintenance period) while wearing a FitBit activity monitor and a Freestyle Libre 2 CGM.
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| Active Comparator: Routine Care Usual care already being received for prediabetes as treated by their care team. |
Other: Routine Care
Participant's current prediabetes treatment.
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Outcome Measures
Primary Outcome Measures
- Change in percentage of CGM glucose readings > 120 mg/dL [4.5 months]
Change in percentage of CGM glucose readings > 120 mg/dL from pre-intervention blinded CGM to post-intervention blinded CGM.
Secondary Outcome Measures
- Change in HbA1c [4.5 months]
Change in HbA1c from baseline to post-intervention.
- Change in Glucose Variability [4.5 months]
Change in glucose variability (GV%) as measured by CGM, from baseline to post-intervention.
- Change in Body Mass Index [4.5 months]
Change in Body Mass Index (BMI) from baseline to post-intervention.
- Change in Cardiovascular Risk [4.5 months]
Change in cardiovascular risk as calculated by a validated risk calculator from baseline to post-intervention
- Change in Empowerment [4.5 months]
Change in empowerment as measured by modified Diabetes Empowerment Scale, from baseline to post-intervention.
- Change in Depressive Symptoms [4.5 months]
Change in depression score as measured by PHQ-8 at baseline and post-intervention.
- Change in Diabetes Knowledge [4.5 months]
Change in diabetes knowledge as measured by a modified Diabetes Knowledge Scale from baseline to post-intervention.
- Dietary Habits [4.5 months]
Change in dietary habits as measured by Carbohydrate Routine Consumption Scale from baseline to post-intervention.
- Motivation and Attitudes Toward Changing Health [4.5 months]
Change in Motivation and Attitudes Toward Changing Health (MATCH) score from baseline to post-intervention.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age 25-70 years
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A1C 6.0-6.4
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Documented diagnosis of prediabetes
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Have a smart phone
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Able to read English, as the GEM guide is currently only available in English
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Willing and able to follow the study procedures as instructed
Exclusion Criteria:
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Diagnosis of diabetes mellitus
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Currently taking any diabetes medication
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Currently taking medication that promotes insulin resistance or otherwise interferes with metabolic control (e.g., prednisone)
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Has a condition that precludes a low carbohydrate diet, such as gastroparesis
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Has a physical or medical condition that precludes walking 120 steps per minute for 10 minutes or longer
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Has documented kidney disease that would preclude participation in study per PI discretion
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Active or planned cancer treatment
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Extreme visual or hearing impairment that would impair ability to use real-time CGM
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Pregnant or anticipates becoming pregnant in the next 4 months
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Anticipates moving within the next 4 months
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Treating physician, for any reason, considers their patient inappropriate for the study (e.g., uncontrolled bipolar disease)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Colorado- Anschutz Medical Campus | Aurora | Colorado | United States | 80045 |
Sponsors and Collaborators
- University of Colorado, Denver
- Abbott Diabetes Care
- University of Virginia
Investigators
- Principal Investigator: Tamara Oser, MD, Associate Professor, Dept. Family Medicine
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 21-4931