Immune Cells During Disuse and Recovery

Description

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.

Conditions

Muscle Disuse

Study Overview

Study Details

Study overview

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.

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

Immune Cells During Disuse and Recovery

Condition
Muscle Disuse
Intervention / Treatment

-

Contacts and Locations

Salt Lake City

The University of Utah, Salt Lake City, Utah, United States, 84112

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

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

Ages Eligible for Study

18 Years to 85 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

University of Utah,

Micah Drummond, PhD, PRINCIPAL_INVESTIGATOR, University of Utah

Study Record Dates

2028-04-30