ClinicalTrials.Veeva

Menu

Vascular Dysfunction During Physical Inactivity

Utah System of Higher Education (USHE) logo

Utah System of Higher Education (USHE)

Status

Completed

Conditions

Aging
Vascular Endothelium
Skeletal Muscle

Treatments

Behavioral: Step Count Reduction

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04872998
IRB #111321
UL1TR002538 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Prolonged periods of reduced activity are associated with decreased vascular function and muscle atrophy. Physical inactivity due to a sedentary lifestyle or acute hospitalization is also associated with impaired recovery, hospital readmission, and increased mortality. Older adults are a particularly vulnerable population as functional (vascular and skeletal muscle mitochondrial dysfunction) and structural deficits (loss in muscle mass leading to a reduction in strength) are a consequence of the aging process. The combination of inactivity and aging poses an added health threat to these individuals by accelerating the negative impact on vascular and skeletal muscle function and dysfunction. The underlying factors leading to vascular and skeletal muscle dysfunction are unknown, but have been linked to increases in oxidative stress. Additionally, there is a lack of understanding of how vascular function is impacted by inactivity in humans and how these changes are related to skeletal muscle function. It is the goal of this study to investigate the mechanisms that contribute to disuse muscle atrophy and vascular dysfunction in order to diminish their negative impact, and preserve vascular and skeletal muscle function.

Enrollment

14 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Individuals who have recently undergone surgery or injury requiring inactivity

Exclusion criteria

  • Cardiac abnormalities considered exclusionary by the study physician (congestive heart failure, coronary artery disease, right-to-left shunt)
  • Uncontrolled endocrine or metabolic disease
  • Glomerular filtration rate < 45 mL/min/1.73 m^2 or evidence of kidney disease or failure
  • Vascular disease or risk factors of peripheral atherosclerosis
  • Risk of deep vein thrombosis including family history of thrombophilia, pulmonary emboli, deep vein thrombosis
  • Use of anticoagulant therapy
  • Elevated systolic pressure > 180 or a diastolic blood pressure > 110
  • Implanted electronic devices such as pacemakers, 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 or body mass index > 35 kg/m^2
  • Inability to abstain from smoking for duration of study
  • History of > 20 pack per year smoking
  • Positive for human immunodeficiency virus, hepatitis B or hepatitis C
  • Recent anabolic or corticosteroids use (within 3 months)
  • Subjects with hemoglobin or hematocrit lower than accepted lab values
  • Agitation/aggression disorder
  • History of stroke with motor disability
  • Recent history (< 12 months) of gastrointestinal bleed
  • Depression diagnosis
  • Alcohol or drug abuse
  • Liver disease (AST/ALT 2 times above the normal limit, hyperbilirubinemia)
  • Respiratory disease (acute upper respiratory infection, history of chronic lung disease with resting oxygen saturation < 97% on room air)
  • Pregnancy

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

14 participants in 1 patient group

Reduced Activity
Experimental group
Description:
Reduction of daily step count by 70% for two weeks, followed by two week recovery to normal activity level
Treatment:
Behavioral: Step Count Reduction

Trial documents
2

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems