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Clinical Trials/NCT03856606
NCT03856606
Completed
Not Applicable

The Effects of Interrupting Prolonged Sitting With Intermittent Exercise on Postprandial Lipemia

University of Texas at Austin1 site in 1 country8 target enrollmentFebruary 20, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Metabolic Syndrome X
Sponsor
University of Texas at Austin
Enrollment
8
Locations
1
Primary Endpoint
Plasma Triglycerides
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to investigate the effect of interrupting prolong sedentary behavior with interval exercise on postprandial metabolism following a high fat glucose tolerance test.

Detailed Description

All subjects complete two trials in a randomized crossover design, with each trial occurring over 4 days with a minimum of seven days between trials. The first two days of each trial serve as a control period allowing for familiarization and the control of physical activity and calorie consumption prior to the intervention. Following each control period, subjects then perform one of the interventions on Day 3. The interventions consist of either eight-hours of prolonged sitting, or eight hours of sitting interrupted every hour by five sprints lasting 4 seconds each using the interval exercise. On day 4, all subjects will undergo a high fat glucose tolerance test to determine the body's ability to clear triglycerides from the blood as well as insulin/glucose response and substrate oxidation. Blood samples will be assayed for the previously mentioned substances and postprandial gas collection will be analyzed via indirect calorimetry.

Registry
clinicaltrials.gov
Start Date
February 20, 2018
End Date
July 8, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Edward F. Coyle

Professor

University of Texas at Austin

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • cardiovascular problems (e.g. pre-existing heart issues, coronary artery disease, hypertension, etc.)
  • respiratory problems
  • musculoskeletal problems that prevent prolonged sitting or exercise
  • susceptibility to fainting
  • Pregnancy

Outcomes

Primary Outcomes

Plasma Triglycerides

Time Frame: 6-hours

Areas under the curve for triglyceride concentration will be calculated for hourly samples from a 6-hour lipid tolerance test

Secondary Outcomes

  • Plasma Glucose(6-hours)
  • Plasma Insulin(6-hours)

Study Sites (1)

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