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The Acute Effect of and Energy Drink vs. Water Consumption on MAP, HR, and Energy Metabolism

The Acute Effect of and Energy Drink vs. Water Consumption on MAP, HR, and Energy Metabolism

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06330649
Enrollment
32
Registered
2024-03-26
Start date
2024-01-01
Completion date
2024-09-01
Last updated
2025-04-01

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

Conditions

Cardiovascular Diseases, Hypertension, Diet

Keywords

Energy metabolism, Arterial blood pressure, heart rate

Brief summary

The objective of this protocol is to investigate the effect of consumption of a commercially available energy drink beverage on blood pressure, heart rate, and energy metabolism

Detailed description

Energy drink consumption has gained a lot in popularity and represents one of the most rapidly growing segments of the beverage industry. While regularly discussed in media outlets etc. the cardiovascular effects are not well described or well known. For example, the impacts on various cardiovascular parameters range from improved, decreased, to not impacted at all depending on the source. This can be due to a number of reasons including, study protocol design, study population tested, energy drink product used, volume consumed, etc. Accordingly, this study aims to investigate the impact of acute consumption of a standard commercially available can of energy drink beverage on the following parameters. * Arterial blood pressure * Heart rate * Energy metabolism (oxygen consumption and carbon dioxide production It is hypothesized that consumption of a 12 oz energy drink will result in modest elevations in arterial blood pressure, heart rate, and energy metabolism relative to when consuming of an equal volume of water.

Interventions

DIETARY_SUPPLEMENTEnergy Drink

This is a commercially available energy drink

This is a commercially available bottled water

Sponsors

The University of Texas at Arlington
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Intervention model description

Individuals will be randomly assigned to either an experimental or a control condition.

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Between ages 18-30 * Must be free of reported cardiovascular, respiratory, and metabolic diseases. * Must be caffeine naïve * Must be fasted

Exclusion criteria

* Food allergies * pregnant women * Breast feeding women * Individuals with cardiac, cardiovascular, respiratory, metabolic, and/or neurological disorders * taking any prescription vasoactive medications * allergies to spandex/lycra

Design outcomes

Primary

MeasureTime frameDescription
Peripheral blood pressure in millimeters of mercurybaseline & 30, 60, 90, 120 min following beverage consumptionblood pressure will be measured on the upper arm using standard procedures that are done in a doctors office.
Oxygen consumption milliliters per kilogram of body weight per minutebaseline & 30, 60, 90, 120 min following beverage consumptionThis will be assessed using a metabolic cart to measure the amount of oxygen that is consumed by the body.
Heart rate in beats per minutebaseline & 30, 60, 90, 120 min following beverage consumptionHeart will be measured using an electrocardiogram procedures that are done in a doctors office.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026