Automated Insulin Delivery for Type 1 Diabetes
What You Need to Know Before You Apply
What is the purpose of this trial?
Type 1 diabetes is a common chronic medical condition among youth in the US that requires intensive glycemic management to prevent long-term morbidity and mortality. Current pediatric diabetes care in the US underutilizes automated insulin delivery (AID) systems, which are the best available tools for promoting tight glycemic control while reducing user burden. This proposal aims to support early and sustained use of AID systems by examining and optimizing conditions, evaluating glycemic outcomes, and identifying contextual facilitators and barriers of implementation.
Who Is on the Research Team?
David Maahs, MD, PhD
Principal Investigator
Stanford University
Are You a Good Fit for This Trial?
Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants initiate early use of an automated insulin delivery system using either Tandem Mobi or Tandem X2 for approximately 2 months
Follow-up
Participants are monitored for sustained use of the AID system and glycemic outcomes
What Are the Treatments Tested in This Trial?
Interventions
- Tandem Automated Insulin Delivery System
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Participants will choose an automated Insulin Device either Tandem Mobi or Tandem X2. The participants will use the device to initiate early pump usage. Participants will use pump for approximately 2 Months, but may vary slightly upon individual insurances. The dose of insulin will vary between patient to patient based on food intake. Participants will complete surveys regarding their perspectives and experiences with the study intervention.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Stanford University
Lead Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborator
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