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Impact of Cocoa Flavanols on Pulmonary Oxygen Uptake Kinetics and Exercise Tolerance in Sedentary Middle-aged Adults

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04370353
Enrollment
18
Registered
2020-04-30
Start date
2018-04-01
Completion date
2019-06-07
Last updated
2020-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging, Sedentary Behavior

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.

Interventions

DIETARY_SUPPLEMENTCocoa flavanols

Flavonoid-rich cocoa powder, containing 100mg total flavanols per 316mg.

DIETARY_SUPPLEMENTPlacebo supplement

Microcrystalline filler, containing 0mg total flavanols.

Sponsors

Liverpool John Moores University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
35 Years to 55 Years
Healthy volunteers
Yes

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

* Smokers * 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

Design outcomes

Primary

MeasureTime frameDescription
Oxygen uptake kineticsOver 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.
Exercise toleranceOver 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.

Secondary

MeasureTime frameDescription
Blood lactateOver 3 week period (After 7 days of each intervention). Measured immediately before and after exerciseA finger prick blood sample will be taken to measure blood lactate pre- and post-exercise of each transition using a hand-held automated blood lactate analyser
Heart rateOver 3 week period (After 7 days of each intervention). Measured during the length of each exercise transition (9 minutes for each moderate intensity bout).Heart rate will be measured during moderate and severe-intensity exercise bouts, by short-range telemetry.
Perceived workloadOver 3 week period (After 7 days of each intervention). Measured immediately before and after exercisePerceived mental workload will be measured pre and post exercise using NASA Task Load Index and BORG rating of perceived exertion scale.
Physical activity and sedentary behaviourOver 3 week period (In the 6 days preceding experimental testing)Physical activity levels will be assessed in the 6 days prior to visiting the laboratory by an accelerometer, worn on the hip during waking hours.
Blood pressureOver 3 week period (After 7 days of each intervention). Measured over 5 minutes before any exercise testing.Systolic and diastolic blood pressure will be assessed following 10 min of seated rest using an automated sphygmomanometer

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026