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Clinical Trials/NCT04370353
NCT04370353
Completed
Not Applicable

Investigating the Impact of Cocoa Flavanol Supplementation on Pulmonary Oxygen Uptake Kinetics and Exercise Tolerance in Sedentary Middle-aged Adults

Liverpool John Moores University1 site in 1 country18 target enrollmentApril 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aging
Sponsor
Liverpool John Moores University
Enrollment
18
Locations
1
Primary Endpoint
Exercise tolerance
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

In recent years, there has been significant interest in dietary flavonoids (biologically active plant-derived compounds) as potential therapeutics. This is due to the capacity of flavonoids to enhance processes related to energy metabolism and cardiovascular health. We are interested in implementing a short-term supplementation regime (daily cocoa-flavanoid ingestion), in order to explore the possible beneficial effects of flavonoid-based interventions on responses to exercise. Hence, the objective of our study is to examine the impact of short term cocoa-flavanoid supplementation on processes related to energy use (oxygen utilisation). Our aim is to develop a novel intervention which improves cardiovascular health and enhances exercise tolerance.

Registry
clinicaltrials.gov
Start Date
April 1, 2018
End Date
June 7, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Aged 35-55 years
  • Healthy (no known cardiovascular or metabolic disorders e.g. diabetes)
  • Do not engage in regular structured physical training (i.e. less than two sessions for 60 minutes per week, for at least 1 year

Exclusion Criteria

  • Medical history of cardiovascular and/or metabolic disease, including diabetes and abnormal blood pressure
  • Family history of cardiovascular disease
  • Currently taking any medication
  • Asthmatic
  • Currently suffering from musculoskeletal injury
  • Younger than 35 or older than 55 years old
  • Known food allergies or special dietary requirements
  • Currently taking any dietary supplements
  • Currently engaging in \>2 hours structured training per week

Outcomes

Primary Outcomes

Exercise tolerance

Time Frame: Over 3 week period (After 7 days of each intervention).

Participants capacity to exercise to the limit of tolerance, measured to the nearest second. Participants are instructed to exercise at a severe-intensity exercise load (representative of 60% ∆), on a cycle ergometer until volitional exhaustion.

Oxygen uptake kinetics

Time Frame: Over 3 week period (After 7 days of each intervention). Oxygen uptake measured for 9 minutes continuously during exercise bouts (3 min warm up period and 6 minutes of exercise transition)

Oxygen uptake kinetics (including time constant, time delay and amplitude of the fundamental oxygen uptake response) will be determined by modelling oxygen uptake during exercise using a mono exponential function. The oxygen uptake data is measured on a breath-by-breath basis during exercise (on a cycle ergometer) using a gas analysis system and face mask. Oxygen kinetics will be measured during three moderate-intensity step exercise tests (at 80% of the gas exchange threshold) and during one severe-intensity (60%∆) step exercise test that is completed to failure.

Secondary Outcomes

  • Heart rate(Over 3 week period (After 7 days of each intervention). Measured during the length of each exercise transition (9 minutes for each moderate intensity bout).)
  • Perceived workload(Over 3 week period (After 7 days of each intervention). Measured immediately before and after exercise)
  • Blood pressure(Over 3 week period (After 7 days of each intervention). Measured over 5 minutes before any exercise testing.)
  • Blood lactate(Over 3 week period (After 7 days of each intervention). Measured immediately before and after exercise)
  • Physical activity and sedentary behaviour(Over 3 week period (In the 6 days preceding experimental testing))

Study Sites (1)

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