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NCT Number: NCT04575844

Effects of Exercise and GLP-1 Agonism on Muscle Microvascular Perfusion and Insulin Action in Adults With Metabolic Syndrome

The primary objective of this study is to examine whether exercise training alone, liraglutide treatment alone or exercise training plus liraglutide treatment increases cardiac and skeletal muscle microvascular blood volume, improves vascular function of the conduit vessels, and enhances insulin's metabolic action in humans with Metabolic Syndrome. Subjects will be randomized to one of the 4 groups: control, exercise training, liraglutide treatment, and exercise + liraglutide. They will be studied at the baseline and then after 24 weeks of intervention.

Recruiting

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Key information

Age range

21 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

About this study

Our hypothesis is that sustained activation of the GLP-1 receptor with Liraglutide and exercise training each will enhance microvascular insulin responses and angiogenesis in both cardiac and skeletal muscle to increase muscle insulin delivery and action and the combination of both is more effective than either alone in adults with metabolic syndrome.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female ≥21 and ≤60 years old.
  • Body mass index >25 and ≤35 kg/m2 and is weight stable (<5 kg weight change in the past 6 months). BMI is limited to ≤35 kg/m2 for easier vascular access and cardiac imaging.
  • Meet 3 of 5 National Cholesterol Education Program Adult Treatment Panel III Metabolic Syndrome criteria:
  • Increased waist circumference (≥102 cm in men; ≥88 cm in women)
  • Elevated triglycerides (≥150 mg/dl)
  • Reduced HDL-cholesterol (<40mg/dl in men, <50 mg/dl in women)
  • High blood pressure (≥130 mmHg systolic or ≥85mmHg diastolic)
  • Elevated fasting glucose (≥100 mg/dl)
  • Subject may participate if on the following drugs, provided the drug doses have been stable for at least 3 months.
  • Ace inhibitor
  • ARB
  • HMG CoA reductase inhibitor
  • Beta blocker
  • Calcium channel blockers
  • Alpha-adrenergic antagonist
  • Statin

Exclusion criteria

  • A diagnosis of any type of diabetes or history of diabetes medication use
  • 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) or hypercholesterolemia (>260 mg/dl)
  • Subjects with BP>160/90
  • 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
  • Subjects with contraindications to participation in an exercise training program
  • Allergic to perflutren
  • A prior use of Liraglutide

Treatment and study plan

liraglutide

Drug

24 weeks of Liraglutide

Exercise training

Other

24 weeks of Exercise training

Liraglutide + Exercise training

Drug

24 weeks of Liraglutide + Exercise training

Primary outcomes

  1. Microvascular Blood Volume - change from baseline

    Time frame: 24 weeks

    measured at baseline and 24 weeks

Secondary outcomes

  1. Augmentation Index - change from baseline

    Time frame: 24 weeks

    measured at baseline and 24 weeks

  2. Flow Mediated Dilation

    Time frame: 24 weeks

    measured at baseline and 24 weeks

  3. Pulse Wave Velocity

    Time frame: 24 weeks

    measured at baseline and 24 weeks

  4. Post Ischemic Flow Velocity - change from baseline

    Time frame: 24weeks

    measured at baseline and 24 weeks

  5. Insulin Sensitivity - change from baseline

    Time frame: 24 weeks

    measured at baseline and 24 weeks

Study contacts

Contact information is provided by the study sponsor or research team.

Lee Hartline, MEd

CONTACT

[email protected]

434-924-5247

Linda Jahn, MEd

CONTACT

[email protected]

434-924-1134

Sponsors and collaborators

Lead sponsor

University of Virginia

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  • National Institutes of Health (NIH)

Registry information

Acronym: ZQL008

Important dates

Study start
2020
Primary completion
2027
Study completion
2027
First posted
Oct 5, 2020
Registry last updated
May 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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