Many adults in the United States regularly consumer energy drinks. Currently, the safety of energy drinks is still questionable and there are many reports associating energy drinks with adverse events including hospitalizations and deaths. Previous research shows that energy drink can affect heart rhythm and elevate blood pressure. However, these studies use a higher volume (32 ounces) of energy drinks than those available in the market (24 ounces). The purpose of this study is to study if 24-ounce energy drinks can significantly affect heart rhythm and elevate blood pressure when compared to a placebo.
The study is a randomized, double blind, controlled, crossover study comparing the effect of energy drinks and placebo on cardiovascular parameters including heart rhythm and blood pressure. Subjects who contact the PI for interest in study participation will be scheduled a time to study facility for initial evaluation on eligibility criteria. At initial evaluation, participants will be informed about the study details, presented with Informed Consent Document (ICD), and be asked to sign the appropriate forms voluntarily if they decide to participate. Once consented, participants will be asked a series of questions and screened for blood pressure and heart rhythm parameters to determine eligibility to enroll. If patient is eligible to enroll, they will be allocated a randomized identification number. Participants will be randomly assigned to consume either two-12 oz bottles of energy drink and two-12 oz bottles of control drink on 2 separate days. The study will occur over approximately 8 days with each session taking about 5 hours per day. Each session will have 6 days between each other. Participants will be expected to refrain from any products containing caffeine or alcohol 48 hours and fast 10 hours before each study visit. At the beginning of each study visit, baseline measurements of ECG, blood pressures, and heart rate will be obtained prior to consuming study drinks. Repeat measurements will be obtained every 60 minutes after consumption over 4 hours.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Enrollment
20
Two 12 oz bottles of commercially available energy drink
Two 12 oz bottles placebo drink. Placebo drink will contain carbonated water, lime juice, and cherry flavoring.
University of Pacific
Stockton, California, United States
QTc interval
Maximum change in QTc interval from baseline in each of 2 arm
Time frame: Measurements are obtained at baseline and every 60 minutes after study drink consumption over 4 hours
Central systolic blood pressure
Maximum change in central systolic blood pressure from baseline in each of 2 arm
Time frame: Measurements are obtained at baseline and every 60 minutes after study drink consumption over 4 hours
QT interval
Maximum change in QT interval from baseline in each of 2 arm
Time frame: Measurements are obtained at baseline and every 60 minutes after study drink consumption over 4 hours
PR interval
Maximum change in PR interval from baseline in each of 2 arm
Time frame: Measurements are obtained at baseline and every 60 minutes after study drink consumption over 4 hours
QRS duration
Maximum change in QRS duration from baseline in each of 2 arm
Time frame: Measurements are obtained at baseline and every 60 minutes after study drink consumption over 4 hours
Heart rate
Maximum change in heart rate from baseline in each of 2 arm
Time frame: Measurements are obtained at baseline and every 60 minutes after study drink consumption over 4 hours
Central diastolic blood pressure
Maximum change in central diastolic blood pressure from baseline in each of 2 arm
Time frame: Measurements are obtained at baseline and every 60 minutes after study drink consumption over 4 hours
Peripheral systolic and diastolic blood pressure
Maximum change in peripheral systolic and diastolic blood pressures in each of 2 arm
Time frame: Measurements are obtained at baseline and every 60 minutes after study drink consumption over 4 hours
Augmentation index
Maximum change in augmentation index from baseline in each of 2 arm
Time frame: Measurements are obtained at baseline and every 60 minutes after study drink consumption over 4 hours
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.