Mode
Text Size
Log in / Sign up
N/A N=30 Randomized Diagnostic

Exercise Detection Study

Type 1 Diabetes

Enrolled (actual)
30
Serious AEs
0.0%
Results posted
Jul 2019
Primary outcome: Primary: Mean Change in Sensor Glucose in Subjects With Type 1 Diabetes — -26.4; 12.0 mg/dL

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Aerobic Exercise (Behavioral); Resistance Exercise (Behavioral)
Age
Adult · 21+ yrs
Sex
All
Sponsor
Oregon Health and Science University
Primary completion
Feb 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Mean Change in Sensor Glucose in Subjects With Type 1 Diabetes
-26.4; 12.0

Summary

The risk of hypoglycemia in individuals with type 1 diabetes increases considerably during exercise. As a result, many patients with type 1 diabetes experience fear of and reluctance to pursue physical activity, in order to avoid the discomforting symptoms associated with hypoglycemia. The bi-hormonal artificial pancreas, a device used for automatic delivery of insulin and glucagon subcutaneously to subjects with type 1 diabetes, is paving the way to revolutionize the management of this disease. The investigator's group has recently completed a study of the bi-hormonal artificial pancreas system during exercise, suggesting reduced hypoglycemia around the exercise period. In order to prepare for a future home study, the ability to detect, grade, and classify physical activity so as to appropriately adjust system parameters is vital in helping to prevent exercise induced hypoglycemia in the home setting. This study is designed to collect 3-axis accelerometry data and heart rate data during a variety of different home activities, as well as during formal exercise in both healthy subjects and subjects with type 1 diabetes. Additionally, the investigators will observe the change in glucose levels before and after exercise in subjects with type 1 diabetes.

Eligibility Criteria

TYPE 1 DIABETIC SUBJECT CRITERIA

Inclusion criteria

  • Male or female subjects 21 to 45 years of age with a diagnosis of T1D for at least 6 months on an insulin pump.
  • Physically active on a regular basis, i.e. at least 3 days of scheduled physical activity per week and willing to perform approximately 60 minutes of exercise (as determined by the investigator after reviewing the subjects activity level).
  • Willingness to follow all study procedures.
  • Willingness to sign informed consent and HIPAA documents.

Exclusion criteria

a. Pregnancy or Lactation: i. For women of childbearing potential, there is a requirement for a negative urine pregnancy test. b. Any cardiovascular disease, defined as a clinically significant EKG abnormality at the time of screening or any history of: stroke, heart failure, myocardial infarction, angina pectoris, or coronary arterial bypass graft or angioplasty. Diagnosis of 2nd or 3rd degree heart block or any non-physiological arrhythmia judged by the investigator to be exclusionary. c. Renal insufficiency (GFR < 60 ml/min, using the MDRD equation as report by the OHSU laboratory). d. Hematocrit of less than or equal to 34%. e. History of severe hypoglycemia during the past 12 months prior to screening visit or hypoglycemia unawareness as judged by the investigator. f. Adrenal insufficiency. g. Any active infection. h. Known or suspected abuse of alcohol, narcotics, or illicit drugs (except marijuana use).

i. Seizure disorder. j. Active foot ulceration. k. Severe peripheral arterial disease characterized by ischemic rest pain or severe claudication. l. Major surgical operation within 30 days prior to screening. m. Use of an investigational drug within 30 days prior to screening. n. Chronic usage of any immunosuppressive medication (such as cyclosporine, azathioprine, sirolimus, or tacrolimus). o. Bleeding disorder, treatment with warfarin, or platelet count below 50,000. p. Current administration of oral or parenteral corticosteroids. q. Any life threatening disease, including malignant neoplasms and medical history of malignant neoplasms within the past 5 years prior to screening (except basal and squamous cell skin cancer). r. Any concurrent illness, other than diabetes, that is not controlled by a stable therapeutic regimen. s. Beta blockers or non-dihydropyridine calcium channel blockers. t. A positive response to any of the questions from the Physical Activity Readiness Questionnaire, see Appendix A. u. Any chest discomfort with physical activity, including pain or pressure, or other types of discomfort. v. Any clinically significant disease or disorder which in the opinion of the Investigator may jeopardize the subject's safety or compliance with the protocol.

HEALTHY SUBJECT CRITERIA

Inclusion Criteria

  • Male or female subjects 21 to 45 years of age.
  • Physically active on a regular basis, i.e. at least 3 days of scheduled physical activity per week and willing to perform approximately 60 minutes of exercise (as determined by the investigator after reviewing the subjects activity level).
  • Willingness to follow all study procedures.
  • Willingness to sign informed consent and HIPAA documents.

Exclusion criteria

  • Pregnancy or Lactation: For women of childbearing potential, there is a requirement for a negative urine pregnancy test.
  • Any history or evidence of renal insufficiency, adrenal insufficiency, liver disease or anemia.
  • A history of cerebrovascular disease or coronary artery disease (or angina) regardless of the time since occurrence.
  • Congestive heart failure, New York Heart Association (NYHA) any class.
  • Diagnosis of 1st, 2nd or 3rd degree heart block or any arrhythmia judged by the investigator to be exclusionary.
  • Any condition which, in the opinion of the investigator, makes it difficult to engage in vigorous physical activity.
  • Any active infection.
  • Severe peripheral arterial disease characterized by ischemic rest pain or severe claudication.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02688218). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search