The Effects of Prolonged Standing Compared to Prolonged Sitting on Postprandial Lipemia
NCT ID: NCT03089437
Last Updated: 2018-10-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
12 participants
INTERVENTIONAL
2017-03-31
2018-08-11
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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Prolonged Standing
Subject stand for 12 hours. The following day the subject will undergo a high fat tolerance test. Order of sitting/standing will be random and each subject will perform both interventions.
Prolonged Standing
Subject will stand for 12 hours and undergo a high fat tolerance test the subsequent day
Prolonged Sitting
Subject sit for 12 hours. The following day the subject will undergo a high fat tolerance test. Order of sitting/standing will be random and each subject will perform both interventions.
Prolonged Sitting
Subject will sit for 12 hours and undergo a high fat tolerance test the subsequent day
Interventions
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Prolonged Standing
Subject will stand for 12 hours and undergo a high fat tolerance test the subsequent day
Prolonged Sitting
Subject will sit for 12 hours and undergo a high fat tolerance test the subsequent day
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* coronary artery disease
* hypertension
* respiratory problems
* musculoskeletal problems that prevent prolonged standing or sitting
* obesity
* susceptibility to fainting
18 Years
40 Years
ALL
Yes
Sponsors
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University of Texas at Austin
OTHER
Responsible Party
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Edward F. Coyle
Dr.
Locations
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University of Texas at Austin Human Performance Laboratory
Austin, Texas, United States
Countries
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Other Identifiers
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2016-12-0031
Identifier Type: -
Identifier Source: org_study_id
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