ClinicalTrials.Veeva

Menu

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

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Completed

Conditions

Hyperinsulinism
Glucose Metabolism Disorders
Arterial Occlusive Diseases
Insulin Resistance
Cardiovascular Diseases
Metabolic Disease
Metabolic Syndrome X
Vascular Diseases
Arteriosclerosis
Atherosclerosis

Treatments

Behavioral: Prolonged sitting with interval exercise
Behavioral: Prolonged sitting without exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT03856606
2017-11-0141

Details and patient eligibility

About

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.

Full 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.

Enrollment

8 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

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
  • susceptibility to fainting
  • Pregnancy

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

8 participants in 2 patient groups

Prolonged sitting without exercise
Experimental group
Description:
Subjects will be asked to undergo prolonged sitting (\~14 hours) of 1 day and will not be asked to perform interval exercise.
Treatment:
Behavioral: Prolonged sitting without exercise
Prolonged sitting with interval exercise
Experimental group
Description:
Subjects will be asked to undergo prolonged sitting (\~14 hours) of 1 day and will be asked to perform interval exercise every hour on the hour.
Treatment:
Behavioral: Prolonged sitting with interval exercise

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems