AIDANET At Home Study

Launched by SUE BROWN · Jun 17, 2025

Keywords

ClinConnect Summary

This clinical trial is studying a new diabetes management system called AIDANET for people with Type 1 diabetes. The study will compare how well blood sugar is controlled using three different ways of using AIDANET: fully automated control, hybrid control, and a mix of both. Before trying AIDANET, participants will use their usual diabetes devices or a study-provided monitoring system without AIDANET to gather baseline information.

Adults aged 18 and older who have had Type 1 diabetes for at least one year and have used an automated insulin delivery system recently may be eligible. Participants must be currently using insulin and willing to use specific study devices, including a continuous glucose monitor (CGM) and insulin pump, during the study. They also need to have someone nearby who knows how to help in an emergency. Throughout the trial, participants will receive training, wear the study devices at home, and share their data online. The study is not yet recruiting, but it aims to help improve blood sugar control by testing different ways of using this promising technology.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Age ≥18.0 years old at time of consent
• • 2. Clinical diagnosis, based on investigator assessment, of Type 1 Diabetes for at least one year.
• • 3. Having used an Food and Drug Administration (FDA) approved AID system within the last six months (can be intermittent use).
• • 4. Currently using insulin for at least six months.
• • 5. Willingness to switch to use an FDA-approved personal insulin for the study pump (e.g., lispro or aspart, or biosimilar FDA-approved products) as directed by the study team.
• • 6. Has one or more supportive companions knowledgeable about emergency procedures for severe hypoglycemia and able to contact emergency services and study staff who either lives with participant or located within approximately 30 minutes of participant and able to locate participant in the event of an emergency.
• • 7. Participant not currently known to be pregnant or breastfeeding.
• • 8. If participant capable of becoming pregnant, must agree to use a form of contraception to prevent pregnancy while a participant in the study (e.g. hormonal contraception, abstinence from heterosexual intercourse). A negative serum or urine pregnancy test will be required for all participants of childbearing potential. Participants who become pregnant will be discontinued from the study. Also, participants who during the study develop and express the intention to become pregnant within the timespan of the study will be discontinued.
• • 9. Willingness to wear a Dexcom CGM during each of the four study phases.
• • 10. Willingness to use the study AIDANET system (CGM, pump, and phone) during the relevant study periods.
• • 11. Willingness not to start any new non-insulin glucose-lowering agent during the course of the trial.
• • 12. Willingness to participate in all study procedures including in person training.
• • 13. Access to internet at home and willingness to upload data during the study as needed.
• • 14. Investigator has confidence that the participant can successfully operate all study devices and is capable of adhering to the protocol.
• • 15. Participant is proficient in reading and verbal communication in English.
• Exclusion Criteria:
• • 1. Plans to start a new non-insulin glucose-lowering agent (e.g. glucagon-like peptide-1 (GLP-1) receptor agonists, Symlin, (DPP-4 inhibitors, also known as dipeptidyl peptidase 4). Participants may be on a stable dose of such an agent for at least the past month.
• • 2. Current use of sulfonylurea medications.
• • 3. Current use of an Sodium-Glucose Cotransporter 2 (also known as a SGLT-2 or SGLT-1/2 inhibitor) due to risk of euglycemic diabetic ketoacidosis (DKA).
• • 4. Hemophilia or any other bleeding disorder.
• • 5. History of severe hypoglycemic events with seizure or loss of consciousness in the last 12 months.
• • 6. History of DKA event in the last 12 months.
• • 7. Currently on peritoneal or hemodialysis.
• • 8. Currently being treated for adrenal insufficiency.
• • 9. Currently being treated for a seizure disorder.
• • 10. Hypothyroidism or hyperthyroidism is not adequately treated.
• • 11. Use of oral or injectable steroids at the time of enrollment.
• • 12. Known ongoing adhesive intolerance that is not well managed.
• • 13. A condition, which in the opinion of the investigator or designee, would put the participant or study at risk.
• • 14. Participation in another interventional trial at the time of enrollment.
• • 15. Participant with a direct supervisor at work/school who is involved in the conduct of the trial.