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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03098446
Other study ID # 2016-12-0022
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 8, 2017
Est. completion date August 11, 2017

Study information

Verified date October 2018
Source University of Texas at Austin
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the effect of 4 days of sitting and moderate exercise on plasma triglyceride elevation after a meal.


Description:

Subjects will undergo three weeks (two intervention, one washout) of testing during which they will participate in two conditions: 1) prolonged sitting (~14-hours/day) with a 1-hour bout of acute exercise at 65% of pre-intervention VO2max and 2) prolonged sitting (~14-hours/day) without an acute bout of exercise. During each intervention week, subjects will have 2 days of dietary and activity control, followed by 4 days during which prolonged sitting will occur. On the evening of the 4th day, subjects in the exercise group will perform the acute bout of exercise. On day 5, all subjects will undergo a lipid 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.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date August 11, 2017
Est. primary completion date August 11, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

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

- obesity

- susceptibility to fainting

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Prolonged sitting with exercise
Subjects will have a 2-day control period during which step count and diet will be controlled for and recreated for the other trial. Following this 2-day period, they will undergo the prolonged sitting trial with the acute bout of exercise on day 4. Day 5 will consist of the lipid tolerance test to determine the ability of the body to clear triglycerides.
Prolonged sitting without exercise
Subjects will have a 2-day control period during which step count and diet will be controlled for and recreated for the other trial. Following this 2-day period, they will undergo the prolonged sitting trial, but will not be asked to complete an acute bout of exercise on day 4. Day 5 will consist of the lipid tolerance test to determine the ability of the body to clear triglycerides.

Locations

Country Name City State
United States University of Texas at Austin Human Performance Laboratory Austin Texas

Sponsors (1)

Lead Sponsor Collaborator
University of Texas at Austin

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Plasma Triglycerides Areas under the curve for triglyceride concentration will be calculated for hourly samples from a 6-hour lipid tolerance test 6-hours
Secondary Plasma Insulin Areas under the curve for insulin concentration will be calculated for hourly samples from a 6-hour lipid tolerance test 6-hours
Secondary Plasma Glucose Areas under the curve for glucose concentration will be calculated for hourly samples from a 6-hour lipid tolerance test 6-hours
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