Recruiting

Artificial Pancreas

Sponsor:

University of Illinois at Chicago

Code:

NCT05145374

Conditions

Type 1 Diabetes

Eligibility Criteria

Sex: All

Age: 20 - 60

Healthy Volunteers: Not accepted

Study Details

Brief summary:

The objective of this proposal is to demonstrate a viable, functionally integrated multivariable artificial pancreas (mvAP) that will address meal, physical activity (PA) and acute psychological stress (APS) challenges without any manual inputs to better regulate glucose levels of people with diabetes. Acute psychological stress and many other forms of PA besides planned exercise can affect blood glucose levels and cause challenges to maintaining euglycemia for people with type 1 diabetes mellitus (T1DM). Various PA and APS affect the metabolism and sensitivity to insulin in different ways. Hence, their types, intensities and durations, and their individual and concurrent presence must be detected in order to determine the optimal insulin administration. The mvAP approach provides a well-integrated and user-friendly technology with minimal burden on the user and mitigates the effects of unexpected PA and APS inducements. Twenty subjects with type 1 diabetes (ages 18-60) who use insulin pumps enrolled in this study. The study will take place at the UIC-College of Nursing Diabetes and Exercise Laboratory. The protocol will include 1 screening visit and 5 sessions at the laboratory. The primary activities at each meeting will include: (1) screening; (2) measurement of peak exercise capacity; (3) estimation of maximal strength from submaximal strength tests; (4) Trier Social Stress Test; (5) submaximal bouts of aerobic and resistance exercise, and activities of daily living with and without stress (e.g., mental calculations, video games). These activities will be included visit 3, 4 and 5 as appropriate. In addition, subjects will perform activities at home include: housekeeping chores, stationary bike (if available); treadmill (if available); walking; and light weights (if available). Periodically, the research assistant will call the subject during these times and ask them to perform stress-inducing activities while performing the activity. The stress inducing activities will include mental challenges such as a mathematical computation while performing the activity. The subjects will be called at home 3-5 times during the study. The fully automated algorithm will be tested in a home setting, however, the methodology will be developed and approved for testing later in the study.

Conditions

Type 1 Diabetes

Study ID

NCT05145374

Start date

Jul 1, 2022

Status verified date

Aug, 2024

Completion date

Sep 1, 2025

Anticipated

Primary completion date

Jul 15, 2025

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 20 - 60

Healthy Volunteers: Not accepted

Inclusion Criteria:

Men and Women with T1DM

Insulin pump users

Exclusion Criteria:

  • Metabolic instability as evidenced by hospitalizations for diabetes or other diabetes-related complications (e.g., diabetic ketoacidosis and hypoglycemic seizures) within the preceding three months;
  • Severe macrovascular disease, as evidenced by severe peripheral artery disease; history of myocardial infarction, heart failure, thromboembolic disease, or unstable angina; uncontrolled hypertension; abnormal resting EKG;
  • Maximal exercise stress test with significant brady/tachy arrhythmia, ectopic beats, bundle branch block, or signs of acute ischemia;
  • Severe microvascular disease as evidenced by history of vision-threatening proliferative or non-proliferative retinal disease; kidney disease;
  • Any uncontrolled non-musculoskeletal condition that would limit the subject's ability to participate in the exercise program (e.g., chronic obstructive airways disease);
  • Musculoskeletal conditions such as neurological or orthopedic conditions affecting lower limb strength and mobility (e.g., stroke; insensitive foot);
  • Pregnancy;
  • Documented medical condition or physical impairment that is judged by the health care practitioner to contraindicate exercise.

Study Design

Enrollment

20 participants

Anticipated

Interventions and Outcome Measures

Arms

Stressful Stimuli

Participation in meal, exercise, sleep activities alone or in combination with stressful stimuli.

Primary outcome measure

  • Measurement of Glucose Concentration [ Time Frame: 2 years ]

Central Contacts and Locations

Central contacts

Locations

University of Illinois Chicago

Recruiting

Chicago, Illinois, United States, 60612

Contacts

Laurie T Quinn, PhD

312-771-6497lquinn1@uic.edu

More Information

Sponsor

University of Illinois at Chicago

Last update posted

Aug 28, 2024

Last verified

Aug, 2024

Keywords

  • Physical Activity
  • Psychological Stress
  • Artificial Pancreas
  • Sleep
  • Stress

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by University of Illinois at Chicago on 2024-08-28.