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Clinical Trial Summary

This study is evaluate the superior efficacy of a Continuous Glucose Monitor (CGM)-based advisory system in Type 1 Diabetes Mellitus (T1DM), as compared to Sensor Augmented Mode (SAM) therapy, and with characterizing the impact of psycho-behavioral factors on system performance, which will enable system individualization and lead to automated adaptation of advice delivery to optimize glycemic control and reduce the system's psychological impact.


Clinical Trial Description

Four cohorts of about 25 participants each (expected retention 20 per cohort). Each cohort will continue for ~7 months. Following recruitment, screening, and a run-in period of SAM, participants will be randomized into one of two groups: escalation vs. de-escalation of devices and function. Each treatment modality (SAM - Sensor-Augmented Mode, PF - Personalized Feedback, DSS - Decision Support Systems) will continue for about 8 weeks, with the last 4 weeks used to assess glucose variability (GV) from CGM data. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04443153
Study type Interventional
Source University of Virginia
Contact Marc Breton, PhD
Phone 434-982-6484
Email mb6nt@virginia.edu
Status Recruiting
Phase N/A
Start date September 4, 2020
Completion date July 31, 2024

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