What this study is
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.
What's being tested
- Limb immobilization
Intervention · OTHER
Participants will undergo a 2-week period of leg immobilization
Study details
- Official title
- Muscle Immune Cells During Disuse and Recovery in Aging and Metabolic Disease
- Sponsor
- University of Utah
- Conditions
- Muscle Disuse
- Enrolling
- 45 people
- Starts
- 2022-05-15
- Est. completion
- 2028-04-30
- Design
- Open-label, single group
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years – 85 YearsSex ALLHealthy volunteers AcceptedYou may qualify if
- Age between 18-35 and 60-85 yrs
- Ability to sign informed consent
- Free-living, prior to admission
You can't join if
- 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
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openThe University of Utah
Salt Lake City, Utah, United States
- Micah Drummond, PhD · Contact8015877764
- Contactmicah.drummond@hsc.utah.edu
- Micah Drummond · Principal investigator
Recruiting
Study team
Sponsor
University of Utah
Study ID 130232
Principal investigator
Micah Drummond, PhD
University of Utah
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.