Study Results
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View full resultsBasic Information
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COMPLETED
NA
9 participants
INTERVENTIONAL
2021-10-08
2024-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
PREVENTION
NONE
Study Groups
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Stationary Cycling
All participants will complete one, 60-minute bout of stationary cycling
Exercise Mode
Stationary cycling or treadmill walking
Treadmill Walking
All participants will complete one, 60-minute bout of treadmill walking
Exercise Mode
Stationary cycling or treadmill walking
Interventions
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Exercise Mode
Stationary cycling or treadmill walking
Eligibility Criteria
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Inclusion Criteria
* All volunteers must be accustomed to performing 60 minutes of vigorous cycling and treadmill exercise
Exclusion Criteria
* hepatobiliary disease, defined as liver function tests (AST, ALT) \>1.5 times the upper limit of normal
* thyroid dysfunction, defined as an ultrasensitive thyroid stimulating hormone (TSH) \<0.5 or \>5.0 mU/L
* serum Ca \<8.5 or \>10.3 mg/dL; 5) serum 25(OH)D \<20 ng/mL
* uncontrolled hypertension, defined as resting systolic blood pressure (BP) \>150 mmHg or diastolic BP \>90 mmHg
* history of type 1 or type 2 diabetes
* cardiovascular disease; defined as subjective or objective indicators of ischemic heart disease (e.g., angina, ST segment depression) or serious arrhythmias at rest or during the graded exercise test (GXT)
* volunteers who have a positive GXT can be re-considered after follow-up evaluation, which must include diagnostic testing (e.g., stress echocardiogram or thallium stress test) with interpretation by a cardiologist
* anemia, defined as a serum hemoglobin \<12.1 g/dL for women and \<14.3 g/dL for men
* fracture in the past 6 months
* current diagnosis or symptoms of COVID-19
* In the event of abnormal BP, live function, TSH, 25(OH)D, or hemoglobin values, volunteers can be reassessed, including after appropriate follow-up evaluation and treatment by a primary care provider
* Those who have experienced symptoms of COVID-19 or have been formally diagnosed will be allowed to participate once symptoms have resolved and they are approved to return to exercise by their primary care provider
60 Years
ALL
Yes
Sponsors
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University of Colorado, Denver
OTHER
VA Office of Research and Development
FED
Responsible Party
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Principal Investigators
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Sarah J Wherry, PhD
Role: PRINCIPAL_INVESTIGATOR
Rocky Mountain Regional VA Medical Center, Aurora, CO
Locations
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Rocky Mountain Regional VA Medical Center, Aurora, CO
Aurora, Colorado, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Document Type: Informed Consent Form
Other Identifiers
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F3593-P
Identifier Type: -
Identifier Source: org_study_id
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