Status:
COMPLETED
Continuous Glucose Monitoring in Diabetes and Prediabetes
Lead Sponsor:
Nicole Ehrhardt, MD
Collaborating Sponsors:
DexCom, Inc.
Conditions:
Diabetes Mellitus, Type 2
PreDiabetes
Eligibility:
All Genders
18-55 years
Phase:
NA
Brief Summary
Evaluate the use of brief serial real time continuous monitoring (RT-CGM) as a behavior modification tool in obese patients with prediabetes and diabetes. After receiving RT-CGM, nutrition and exercis...
Eligibility Criteria
Inclusion
- Age 18-55
- Prediabetes (A1c 6.0-6.4) or Diabetes (A1c 7.0-10)
- BMI ≥ 30 kg/m2
- Willing to wear pedometer during study period
- Able to walk 2 city blocks at baseline without assistance (self-reported)
- Reading level at least 6th grade in English
- Expected to remain in local community for at least 4 months
- Either is not treated with or has been on a stable treatment regimen of any of the following medications for a minimum of 3 months prior to Visit 1 (Screening/Enrollment):
- Sulfonylureas
- Biguanidine
- Thyroid replacement therapy
- Glp-1 agonists
- Sodium-glucose co-transporters
- Basal insulin
- Thiazolidinediones
- Hormone replacement therapy (female subjects) estrogen/progesterone products
- Oral contraceptives/birth control (female subjects)
- Antidepressant agents (SSRIs, Paxil, Prozac, Celexa, Zoloft, etc.)
- Is able to read, understand, and sign the Informed Consent Form (ICF) and if applicable, an Authorization to Use and Disclose Protected Health Information form (consistent with Health Insurance Portability and Accountability Act of 1996 \[HIPAA\] legislation), communicate with the investigator, and understand and comply with protocol requirements.
Exclusion
- Women who are pregnant, lactating, planning to become pregnant
- Subjects who are taking amphetamines, anabolic, or weight-reducing agents
- Contraindications to moderate exercise
- Pre-prandial insulin
- On any antipsychotic medication or history of schizophrenia or bipolar disorder
- Daily use of any form of steroid medication (oral, inhaled, injected) within the last 3 months
- Active wounds or recent surgery within 3 months
- Inflammatory disease, or chronic and current use of anti-inflammatory drugs or narcotics
- Active cardiovascular diseases within 12 months of Visit 1, such as myocardial infarction, clinically significant arrhythmia, unstable angina, coronary artery bypass surgery, or angioplasty; or are expected to require coronary artery bypass surgery or angioplasty during the course of the study
- Presence or history of severe congestive heart failure (New York Heart Association Class IV \[CCNYHA 1994\])
- Has evidence of current abuse of drugs or alcohol or a history of abuse that, in the investigator's opinion, would cause the individual to be noncompliant
- Enrolled in another weight loss program
- Already receiving continuous glucose monitoring (CGM)
Key Trial Info
Start Date :
January 10 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 3 2020
Estimated Enrollment :
23 Patients enrolled
Trial Details
Trial ID
NCT03805412
Start Date
January 10 2019
End Date
July 3 2020
Last Update
March 1 2023
Active Locations (1)
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1
GWU Medical Faculty Associates
Washington D.C., District of Columbia, United States, 20037