Skip to main content
Clinical Trials/NCT04277091
NCT04277091
Completed
Not Applicable

The Effect of Upper-body High-intensity Interval Exercise vs. Moderate-intensity Continuous Exercise on Postprandial Metabolism

University of Bath1 site in 1 country11 target enrollmentOctober 21, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
High-Intensity Interval Training
Sponsor
University of Bath
Enrollment
11
Locations
1
Primary Endpoint
Postprandial triglyceride concentrations
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Cycling and running-based high-intensity interval training are well-established to improve a variety of health outcomes. However, the efficacy of upper-body high-intensity interval training, vital for individuals with lower-body impairments, has yet to be well-characterized. The purpose of this study is to compare the effect of a single bout of upper-body high-intensity interval exercise (HIIE) in comparison to traditional moderate-intensity continuous exercise (MICE) on the blood response (e.g. glucose, insulin, fats) following a meal.

This study is recruiting able-bodied adults (aged 18-65 years). Participants will need to attend the laboratory at the University of Bath for two preliminary sessions, and three main study trials.

Detailed Description

The aim of this research is to determine the metabolic responses to a mixed-meal tolerance test following an acute bout of HIIE and an energy-matched MICE bout in able-bodied persons. The hypothesis is that HIIE and MICE will be more effective at reducing the total triglyceride responses compared to a resting control condition. Preliminary measurements: Preliminary testing will include measurements of weight and height. There will also be an assessment of resting metabolic rate and maximal exercise capacity. On a second visit, a HIIE familiarisation session will be performed to determine total energy expenditure of the session. All of the exercise protocols will take place on an arm crank ergometer at the University of Bath. Main trial days: Before all main trials, participants will be asked to refrain from performing any strenuous physical activity in the 48-h prior (i.e. day 0 and 1) and consuming alcohol/caffeine in the 24-h prior (i.e. day 1). On day 1, participants will be asked to record/replicate their diet using a weighed food-diary. Participants will be asked perform exercise (HIIE and MICE only) at 18:00 on day 1, having consumed no food (other than plain water) from 14:00. They will be given a standardised dinner to eat at 20:00, and asked to avoid the ingestion of any further food (other than plain water) for the rest of the evening. On day 2 and upon arrival to the laboratory, a cannula will be inserted into a vein, and a baseline blood sample and expired air sample will be taken. The participant will then be asked to consume a smoothie, consisting of peanut butter, banana, coconut oil, sugar, and chocolate-flavoured whey protein powder. The meal should be consumed within 10 minutes and blood samples will be taken from the cannula at 15, 30, 45 60, and 90 minutes and then at every hour for 5 hours after consumption of the meal to monitor changes in metabolic markers. Expired gas samples will also be taken hourly and indirect calorimetry will be used to estimate relative fat and carbohydrate metabolism in response to the meal.

Registry
clinicaltrials.gov
Start Date
October 21, 2019
End Date
January 1, 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

James Bilzon

Professor

University of Bath

Eligibility Criteria

Inclusion Criteria

  • Non-smoker
  • No history of cardiovascular, metabolic, or neuromuscular disease

Exclusion Criteria

  • Individuals with a nut allergy

Outcomes

Primary Outcomes

Postprandial triglyceride concentrations

Time Frame: 5 hours

Postprandial triglyceride concentrations in serum samples

Secondary Outcomes

  • Heart Rate(HIIE: End of Warm-Up, 8 min, 12 min, 16 min, 20 min, 24 min. MICE: 0, 20, 40, 60, 80, 100% through exercise session (exact time points dependent on exercise time for each participant))
  • Self-efficacy(30 min post-exercise)
  • Postprandial insulin concentrations(5 hours)
  • Rating of Perceived Exertion(HIIE: End of Warm-Up, 8 min, 12 min, 16 min, 20 min, 24 min. MICE: 0, 20, 40, 60, 80, 100% through exercise session (exact time points dependent on exercise time for each participant))
  • Postprandial glucose concentrations(5 hours)
  • Affect(HIIE: End of Warm-Up, 8 min, 12 min, 16 min, 20 min, 24 min. MICE: 0, 20, 40, 60, 80, 100% through exercise session (exact time points dependent on exercise time for each participant))
  • Postprandial substrate oxidation(5 hours)
  • Exercise Enjoyment(30 min post-exercise)

Study Sites (1)

Loading locations...

Similar Trials