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Study identifier: NCT07507708 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Insulin Delivery With Self-Adjusting Closed-Loop and Behavioral Glycemic Control Enhanced by Prediction

Condition: Type 1 Diabetes (T1D)  ·  Sponsor: Sue Brown

PhaseNA
Planned participants20
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study is a randomized cross-over trial comparing AIDANET with Anticipation to AIDANET in FCL without Anticipation. Participants will complete 4 weeks of AID data collection which will be used to establish baseline and initialize the control algorithm. Participants will then be randomized to one of two groups: Group A: AIDANET in FCL with Anticipation (AIDANET+ACL), and Group B: AIDANET in FCL without Anticipation (AIDANET+FCL). The study duration of each group is 4 weeks each. The order of these two phases will be dependent upon randomization.

This description comes directly from the study's public registry record.

Talk to the study team

Andrea Riana, MD  ·  (434) 249-6251  ·  rys6hm@uvahealth.org

Laura Kollar, RN  ·  (434) 982-6479  ·  llk7m@uvahealth.org

Always discuss trial participation with your own doctor first.

Locations (1)

University of Virginia Center for Diabetes TechnologyCharlottesville, Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07507708