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Clinical Trials/NCT05610111
NCT05610111
Completed
Not Applicable

Adaptive Biobehavioral Control (ABC) in a Closed-Loop System: A Randomized Crossover Clinical Trial

Sue Brown1 site in 1 country72 target enrollmentJanuary 18, 2023
ConditionsType 1 Diabetes

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Type 1 Diabetes
Sponsor
Sue Brown
Enrollment
72
Locations
1
Primary Endpoint
CGM-measured percent time in range 70-180 mg/dL
Status
Completed
Last Updated
11 months ago

Overview

Brief Summary

This study is intended to test a Web-based Information Tool (WIT) software providing additional information regarding time in range, GMI, hypo- and hyperglycemia risks, variability tracker, daily glycemic profiles, and potential changes of insulin pump parameters, to users of a commercially available Closed-Loop Control (CLC) System (Control-IQ Technology).

Detailed Description

This is a randomized two-arm crossover group trial in which both groups will use the CLC (Control-IQ) plus WIT. The difference between the two groups will be the order of the interventions. Each group will undergo screening and collection of baseline data from their personal AID system (Control-IQ) followed by randomization 1:1 into two groups. Both groups will have the same three interventions but will progress in the study in a different order allowing for crossover comparisons. The three interventions are: * Use of personal CLC system for 2 weeks * Use of personal CLC system and adding a behavioral adaptation module (BAM) for 4 weeks * Use of personal CLC system and adding the ABC which includes: BAM and PAM (which includes ATM and WST described below) for 16 weeks. The BAM will consist of modules in which information only is given to participants (e.g. time in range, Glucose Management Indicator (GMI), hyper-and hypoglycemic risks, daily glycemic profiles, and variability tracker). The PAM includes auto suggestions for titration of insulin pump parameters every two weeks (ATM) and is aided by a web simulation tool (WST) which can replay 'what if' scenarios for the participant based on various combinations of insulin pump parameter changes.

Registry
clinicaltrials.gov
Start Date
January 18, 2023
End Date
September 28, 2024
Last Updated
11 months ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Sue Brown
Responsible Party
Sponsor Investigator
Principal Investigator

Sue Brown

Study Physician

University of Virginia

Eligibility Criteria

Inclusion Criteria

  • Age ≥18.0 and ≤70 years old at time of consent
  • Clinical diagnosis, based on investigator assessment, of type 1 diabetes for at least one year
  • Currently using an insulin pump for at least six months
  • Currently using insulin for at least six months
  • Currently using the t:slim X2 insulin pump for at least two months
  • Currently using or anticipated to be using the t:slim X2 insulin pump with Control-IQ technology at randomization (Visit 3).
  • Using or willing to use insulin parameters such as carbohydrate ratio and correction factors consistently on their pump in order to dose insulin for meals or corrections
  • Access to internet and willingness to upload data during the study as needed
  • Willing to use an app on a smart phone during the study.
  • For females, not currently known to be pregnant or breastfeeding

Exclusion Criteria

  • Concurrent use of any non-insulin glucose-lowering agent other than metformin or GLP-1 receptor agonists following screening (including pramlintide, DPP-4 inhibitors, SGLT-2 inhibitors, sulfonylureas)
  • A condition, which in the opinion of the investigator or designee, would put the participant at risk or interfere with the completion of the protocol.
  • History of diabetic ketoacidosis (DKA) in the 12 months prior to enrollment
  • Severe hypoglycemia resulting in seizure or loss of consciousness in the 12 months prior to enrollment
  • Currently being treated for a seizure disorder
  • Hemophilia or any other bleeding disorder
  • Planned surgery during study duration
  • Participation in another pharmaceutical or device trial at the time of enrollment or during the study
  • Having a direct supervisor at place of employment who is also directly involved in conducting the clinical trial (e.g., study investigator, coordinator, etc.); or having a first-degree relative who is directly involved in conducting the clinical trial.

Outcomes

Primary Outcomes

CGM-measured percent time in range 70-180 mg/dL

Time Frame: 4 weeks

The primary outcome for this study is CGM-measured percent time in range 70-180 mg/dL over the last 4-week periods on CLC+ABC versus 2 weeks of the current CLC system. The intervention will be considered effective if the CLC+ABC is superior to the CLC alone in a crossover design using a statistical significance of α=0.05. To preserve the overall type 1 error for selected key secondary endpoints, a hierarchical testing procedure will be used. If the primary analysis for time in range described above results in a statistically significant result (p \< 0.05), then testing (similar to the model for the primary outcome) will proceed to the next key secondary outcome metric in the following order entered.

Secondary Outcomes

  • CGM-measured percent above 180 mg/dL during the day(4 weeks)
  • CGM-measured mean glucose(4 weeks)
  • CGM-measured coefficient of variation during the day(4 weeks)
  • CGM-measured percent below 70 mg/dL during the day(4 weeks)

Study Sites (1)

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