Energy Drink Habituation Effects on Young Adults

Healthy Volunteers Clinical Trial

Official title:

Acute Effects of Energy Drink on Hemodynamic and Electrophysiologic Parameters in Habitual and Non-Habitual Caffeine Consumers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04223167
• Other study ID #: 2017/1211
• Status: Completed
• Phase: N/A
• Start date: January 20, 2018
• Est. completion date: May 14, 2019

Study information

• Verified date: January 2020
• Source: Aydin Adnan Menderes University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The consumption of energy drinks has significantly increased in recent years but their adverse effects are not yet efficiently known. The objective of the study is to determine the acute effects of energy drink on habitual and non-habitual caffeine consumers and if caffeine consumption habit causes a difference on the hemodynamic and electrophysiologic parameters.

This study was conducted on 48 students selected from Aydın Adnan Menderes University. Four main groups were determined according to the results of the application acceptance survey. Blood pressure, electrocardiogram, breath rate, haemoglobin oxygen saturation and bioelectrical impedance analysis were measured before consuming the drinks. After consuming the drinks, measurements were repeated at 30 minutes and 60 minutes. In addition to this, Participant's Situation Anxiety Scale was applied.

Description:

In this study, it is aimed to determine the acute effects of energy drink on habitual and non-habitual caffeine consumers and if caffeine consumption habit causes a difference on the hemodynamic and electrophysiologic parameters. In this respect, the complicated human body's reactions to these beverages will be examined in more detail.

Materials and methods Participants Forty eight participants (16 female, 32 male) aged 18-24 were selected from the students which are in the first year of various faculties of Aydın Adnan Menderes University. The individuals were identified by collecting the age, weight, height, BMI, caffeine and energy drink consumption habit information by applicant acceptance questionnaire. According to the results of applicant acceptance questionnaire, those with a body mass index greater than 30 kg/m2, a systemic disease, current alcoholism and smokers were not included in the study. Also, the participants who has previous adverse reactions to energy drinks were excluded to prevent undesired reactions associated with this condition. Based on the applicant acceptance questionnaire 12 subjects were low-habitual caffeine consumers with an estimated daily intake of approximately 130 mg caffeine and named as energy drink 2 (ED2) group, 12 subjects were high-habitual caffeine consumers with an estimated daily intake of approximately more than 200 mg caffeine and named as energy drink 3 (ED3) group, while 24 subjects were caffeine naive (energy drink 1 (ED1) (n=12) and Control (n=12)) . This study conforms to the Declaration of Helsinki and was approved by the Institutional Medical Ethics Committee of Adnan Menderes University (Protocol number: 2017/1211).

Experimental protocol All experiments were performed in a quiet and isolated room from external factors with room temperature of about 20°C and relative humidity between %40 and

60. All participants were advised to avoid alcohol and caffeine containing foods for at least 72 h prior to the test and to come with an overnight (12 h) fasting.

Blood pressure, electrocardiogram, breath rate, haemoglobin oxygen saturation (HOS) and BIA measurements were performed from the participants before the consumption of drinks. After the measurements ED1, ED2 and ED3 groups consumed 473 ml of Red Bull energy drink containing 151.36 mg caffeine and control group consumed the same amount of water within 5 minutes. The measurements were performed again in 30 minutes and 60 minutes. Also, state-trait anxiety inventory test (STAI) was used to assess the physiological stress of the participants.

Blood Pressure Systolic blood pressure (SBP) and diastolic blood pressure (DBP) were measured indirectly by using a stethoscope (Littman Classic II, Saint Paul, USA) and aneroid sphygmomanometer (Welch Allyn Tycos, New York, USA) on each participant left arm in sitting position.

Electrocardiography (ECG) After a 5 min resting in the sitting position ECG recordings were obtained from all the individuals for 5 min in rest. Disposable Ag-AgCl electrodes were placed following the Einthoven triangle configuration. ECG measurement was performed with sampling frequency 200 Hz using ECG100C unit and BIOPAC Acqknowledge acquisition software (Biopac System Inc., Santa Barbara, CA) connected to a personal computer. PR interval, QRS complex and QTc interval values were determined from ECG recordings of the participants. QTc was calculated by Bazett's formula (QTc=QT/RR). Their normal range values are 120-200 ms, normal<140 ms and normal < 400 ms, respectively.

For acquiring the heart rate variability (HRV) time series, Pan and Thompkins algorithm was used. R peaks were detected and R-R intervals are defined. The time duration between two consecutive R peaks is termed as RR interval (tRR). The sample size of the HRV time series is 400. The heart rate (HR) is determined as:

HR=60/t_RR State-trait Anxiety Inventory (STAI) It is a test developed to determine the psychological stress during the study. STAI is defined as state and trait anxiety scale. This test is composed of two parts (40 questions). State Anxiety scale consisting of the first 20 questions was used to obtain information about the acute anxiety state of participants at the time of the study. Each question is evaluated using an ordinal scale (not at all=1, somewhat=2, moderately=3, very much=4). The total score is obtained as the sum of each answer value and gives information about the anxiety state of the participant. A total score of 50 or more is considered as positive pathological anxiety.

Haemoglobin Oxygen Saturation (HOS) HOS was measured by using a fingertip pulse oximeter on the second left finger for 1 min.

Breath Rate Breath rate measurements were taken from the participants by counting the breaths for one minute with the use of a stethoscope (Littman Classic II, Saint Paul, USA).

Bioelectrical Impedance Analysis (BIA) BIA measurements were taken by using In Body 720 before the consumption of the drinks and at 60th minute after the consumption. Each participant was asked to stand on the body composition analyzer after undressing their clothes. In Body 720 has an eight-point tactile electrode system that separately measures the impedance of the arms, trunk and legs. It measures directly the amount of the intracellular water (ICW), extracellular water (ECW), body fat percentage (PBF), body mass index (BMI) and body metabolism rate (BMR).

Statistical analysis Statistical analysis of the data was performed by using SPSS Statistics for Windows, Version 14.0. (SPSS Inc., Chicago, Illinois, USA). For comparing the groups first of all Shapiro-Wilk (SW) normality test was applied to determine the normality of the distribution. If the result of (SW) normality test was bigger than 0.05 the data were normally distributed and were analysed by using one-way analysis of variance (ANOVA) with Bonferroni post-test but if the result was less than 0.05 the data were not normally distributed and were analysed by using Kruskal-Wallis non-parametric test. Repeated ANOVA test was used for the comparison of different measurement time data of the same group. Descriptive statistics were presented as mean ± standard error of the mean (SEM). A p-value of less than 0.05 was considered to indicate statistical significance.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: May 14, 2019
• Est. primary completion date: May 14, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 24 Years

Eligibility

Inclusion Criteria:

• Healthy volunteers between ages 18-24 years

Exclusion Criteria:

• body mass index greater than 30 kg/m2

• a systemic disease

• current alcoholism

• smokers

• the participants who has previous adverse reactions to energy drinks

Related Conditions & MeSH terms

• Healthy Volunteers

Intervention

Dietary Supplement:
• Red Bull Energy Drink
473 ml Reb Bull Energy Drink
• Water
473 ml Water

Locations

Country	Name	City	State
Turkey	Aydin Adnan Menderes University	Aydin

Sponsors (1)

Lead Sponsor	Collaborator
Aydin Adnan Menderes University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in blood pressure from baseline		At baseline and 60 minutes post energy drink and placebo consumption
Primary	Change in heart rate from baseline		At baseline and 60 minutes post energy drink and placebo consumption
Secondary	Change in QTc interval from baseline		At baseline and 60 minutes post energy drink and placebo consumption