RecruitingNot ApplicableNCT04416191

Immune Cells During Disuse and Recovery

Muscle Immune Cells During Disuse and Recovery in Aging and Metabolic Disease


Sponsor

University of Utah

Enrollment

45 participants

Start Date

May 15, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

This is an interventional study enrolling healthy individuals aged 18-35 and 60-85 to understand the recovery of muscle health following a period of inactivity. The enrollment goal is 45 participants. The study will occur over the course of 1-2 months where participants will undergo testing before and after a 2-week limb immobilization period.


Eligibility

Min Age: 18 YearsMax Age: 85 Years

Inclusion Criteria3

  • Age between 18-35 and 60-85 yrs
  • Ability to sign informed consent
  • Free-living, prior to admission

Exclusion Criteria19

  • History of cardiovascular disease (e.g., CHF, CAD, right-to-left shunt)
  • History of endocrine or metabolic disease such as hypo/hyperthyroidism and diabetes
  • History of kidney disease or failure
  • Vascular disease
  • Risk of DVT including family history of thrombophilia, DVT, pulmonary emboli, myeloproliferative diseases including polycythemia (Hb>18 g/dL) or thrombocytosis (platelets>400x103/mL), and connective tissue diseases (positive lupus anticoagulant), hyperhomocystinemia, deficiencies of factor V Leiden, proteins S and C, and antithrombine III
  • Use of anticoagulant therapy (e.g., Coumadin, heparin)
  • Elevated systolic pressure >150 or a diastolic blood pressure > 100
  • Implanted electronic devices (e.g., pacemakers, electronic infusion pumps, stimulators)
  • Cancer or history of successfully treated cancer (less than 1 year) other than basal cell carcinoma
  • Currently on a weight-loss diet
  • Chronic systemic corticosteroid use (≥ 2 weeks) within 4 weeks of enrollment and for study duration (intra-articular/topical/inhaled therapeutic or physiologic doses of corticosteroids are permitted)
  • Androgens or growth hormone within 6 months of enrollment and for study duration (topical physiologic androgen replacement is permitted)
  • History of stroke with motor disability
  • A recent history (<12 months) of GI bleed
  • History of liver disease
  • History of respiratory disease (acute upper respiratory infection, history of chronic lung disease)
  • Pregnancy as determined by a pregnancy test
  • Any staff members who report directly to an investigator or who report to someone who reports directly to an investigator.
  • Any other condition or event considered exclusionary by the PI and faculty physician

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Interventions

OTHERLimb immobilization

Participants will undergo a 2-week period of leg immobilization


Locations(1)

The University of Utah

Salt Lake City, Utah, United States

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NCT04416191


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