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The Effect of Real Time Continuous Glucose Monitoring in Subjects With Pre-diabetes — CGM PreDM  

Pre-diabetes Clinical Trial

Official title:
The Effect of Real Time Continuous Glucose Monitoring in Subjects With Pre-diabetes

Clinical Trial Summary

This study will investigate whether real-time continuous glucose monitoring can be used as a tool for behavior change in people with pre-diabetes.

Clinical Trial Description

The protocol is a prospective, non-blinded, randomized controlled study in persons with newly diagnosed pre-diabetes comparing the effects of real-time continuous glucose monitoring (RT-CGM) combined with diet and lifestyle education to those who have diet and lifestyle education alone. During a "wash-in" phase both groups will wear a masked CGM for 1 week at baseline and again after 12 weeks. Those randomized to the RT-CGM will wear it for 4 cycles of 2 week on/1 week off over the next 12 weeks. Both groups will follow-up with their primary care providers as clinically indicated over the next year with quarterly measurements of blood pressure, weight, and BMI. At the end of this period, they will wear a masked CGM for 1 week. ;

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01741467
Study type Interventional
Source Walter Reed National Military Medical Center
Contact
Status Completed
Phase N/A
Start date May 2012
Completion date August 2016
View Details
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