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NCT07573228Recruiting

Impact of Obesity on Microvascular Insulin Action and Cardiorespiratory Fitness in Type 1 Diabetes

Impact of Obesity on Microvascular Insulin Action and Cardiorespiratory Fitness in Type 1 Diabetes (

Source: ClinicalTrials.gov · Last updated 7 May 2026

Brief summary (registry, in English)

The purpose of this study is: * To see if insulin resistance (how sensitive your muscle tissue is to insulin) is associated with lower cardio fitness in people with Type 1 diabetes compared to healthy controls, before and after a High Intensity Interval Training (HIIT) exercise program. * To see if being overweight and having Type 1 diabetes is associated with lower cardio fitness compared to overweight healthy controls, before and after a HIIT exercise program.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
14 Apr 2026
Start date
23 Feb 2026
Primary completion date
30 Jun 2030
Lead sponsor
University of Virginia
NCT number
NCT07573228

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 23 Feb 2026 to the primary completion date, 30 Jun 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Lab values

  • • Acute or chronic disease other than T1D or obesity
    • History of microvascular or macrovascular diabetes complications
    • History of diabetic ketoacidosis in the past 24 months
    • History of hypoglycemia unawareness
    • Recently active (\>20 min of moderate/high intensity exercise, 2 times/week)
    • Subjects who are smokers or who have quit smoking \<5 years
    • Subjects with hypertriglyceridemia (\>400 mg/dl)
    • Current use of vasoactive medications (i.e. calcium channel blockers, angiotensin-converting enzyme or renin inhibitors, angiotensin-receptor blockers, nitrates, alpha- or beta-blockers, or diuretics).
    • Females taking oral contraceptives in the past 3 months
    • Subjects with a history of significant metabolic, cardiac, cerebrovascular, hematological, pulmonary, gastrointestinal, liver, renal, or endocrine disease or malignancy
    • Pregnant (as evidenced by positive pregnancy test) or nursing women
    • Musculoskeletal condition preventing participation in exercise testing or exercise training
    • History of gastroparesis
    • Pulse oximetry \<90%

Who the study is looking for

  • • Male or female ≥21 and ≤50 years old
    • For persons with T1D: Disease duration ≥ 5 years and HbA1c ≤ 8.5% on multiple daily insulin injection or insulin pump
    • Body mass index: ≥19 and ≤27 kg/m2 for control and T1D, ≥30 and ≤40 kg/m2 (27.5 to 37.5 for Asian Americans) for obesity and T1D + obesity. BMI is limited to ≤40 kg/m2 (37.5 for Asian Americans) for easier vascular access and cardiac imaging.
    • Stable use of non-insulin medications for over 6 months other than estrogen/progesterone containing medications which must be discontinued at least 3 months prior to the study (intrauterine devices may be continued due to limited systemic absorption)

Age in the registry: 21 years to 50 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Virginia
Coordinator of this site? Confirm its status
CharlottesvilleUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.