Effect of Energy Drink on Sport Performance and Psycho-Physiological Responses.
Effects of Energy Drink on Performance and Psycho-Physiological Response to Physical Exercise
1 other identifier
interventional
22
0 countries
N/A
Brief Summary
This work aimed to examine the effects of drinking an "energy drink" upon (i) short-term maximal performance, (ii) reaction times and (iii) psychological factors (i.e., mood state, ratings of perceived exertion (RPE) and affective load) and on physiological parameters such as blood pressure, blood glucose, hematological parameters and other biochemical parameters.
Trial Health
Trial Health Score
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participants targeted
Target at below P25 for not_applicable
Started Jan 2017
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 12, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
January 12, 2017
CompletedFirst Submitted
Initial submission to the registry
April 24, 2019
CompletedFirst Posted
Study publicly available on registry
May 3, 2019
CompletedMay 3, 2019
May 1, 2019
11 days
April 24, 2019
May 1, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (13)
Change in Wingate-test physical performance from PL to RB condition
A calibrated mechanically-braked cycle ergometer (Monark 894; Stockholm, Sweden) interfaced with a microcomputer was utilized for the 30-s Wingate test. Subjects pedaled as fast as possible for 30-s against a constant load calculated according to the participant's body-mass (i.e., 8.7%). After maintaining a constant \~60rpm speed for 4-6-s against minimal resistance, the selected load was applied. The participant sat on the cycle throughout and was strongly encouraged to maximize pedaling rates and to maintain a high speed. Peak and mean power (i.e., average of power output the 30-s) were recorded. The fatigue index was calculated as follows: Fatigue index (%) = \[(peak power-minimal power)/ peak power×100\]. The ICC and SEM showed excellent reliability for peak power (ICC\>0.98, absolute SEM \<0.21), mean power (ICC\>0.98, absolute SEM \<0.23) and fatigue index (ICC\>0.76, absolute SEM \<1.99).
The performance in Wingate test was measured 1 hour following the consumption of supplementations in the first and second test sessions (RB session and PLA session) to assess possible beneficial effect of RB supplementation in physical performance
Change in Reaction Time Performance from PL to RB condition
A simple visual reaction time test assessed alertness and motor reaction-speed. Subjects responded as quickly as possible to presentation of a stimulus (the image of a black box) on a computer screen (15" LCD). When this appears, the participant should press the index finger on a computer key. The signal appeared in random order within 1-10-s time intervals. Each participant was allowed ten attempts and the mean reaction time was calculated, using React! V0.9 software.The ICC and SEM showed excellent reliability for reaction time (ICC\>0.89, absolute SEM \<0.14) measurement.
The reaction time performance was measured 1 hour following the consumption of supplementations in the first and second test sessions (RB session and PLA session) to assess possible beneficial effect of RB in reaction time performance
Change in Strength Physical Performance (i.e., Handgrip) from PL to RB condition
Handgrip strength was recorded by dynamometer (T.K.K. 5401; Takei, Tokyo, Japan). The maximal handgrip force was determined for the dominant hand. Participants exerted their maximal strength for 4-5-s. With the hand hanging downwards, the dynamometer was
Handgrip performance was measured 1 hour following the consumption of supplementations in the first and second test sessions (RB session and PLA session) to assess possible beneficial effect of RB supplementation in strength (i.e., Handgrip) performance
Change in Rating of Perceived Exertion (RPE) and Affective Load from PL to RB condition
The original Borg RPE scale rates exertion subjectively during or after physical exercise on a 15-point scale ranging from six (very very light) to twenty (very very hard). It was used to calculate the affective load; the affective load was obtained as the difference between the perceived exertion (negative affective response) and pleasure scores (positive affective response). For example, with an RPE score of six, the negative affective response is zero and the positive affective response is -14. However, if the RPE score rises to 20, the negative affective response is +14 and the positive affective response is zero. The potential affective load thus ranges from -14 to +14. A negative affective load score indicates the dominance of pleasant affective responses and a positive affective load represents the dominance of unpleasant affective responses.
RPE and Affective Load were measured immediately following the first and second training sessions (RB and PL sessions) to assess any beneficial effect of the consumed RB (1 hour before session) on fatigue and load perception
Change in Mood States (POMS) from PL to RB condition
The evaluation of mood states used the French language version of the POMS questionnaire. Responses to 65 adjectives (ranging from "Zero" (i.e., not at all) to "Four" (i.e., extremely) assessed immediate mood states in seven dimensions: tension, depression, anger, vigor, fatigue, confusion and interpersonal relationships.
POMS was measured immediately following the first and second training sessions (RB and PL sessions) to assess any beneficial effect of the consumed RB (1hour before session) on perception of tension, depression, anger, vigor, fatigue, and confusion
Change in Blood pressure and blood glucose from pre- to post-training session using RB condition
Blood glucose was measured using the electrochemical sensor Rightest GM260 Blood Glucose Monitoring System (Bionime Corporation, Taichung City, Taiwan). The finger tip was pricked with a lancing device, and a specific test strip was soaked with blood was inserted into the measuring apparatus, with an estimate appearing within 5 seconds. Blood pressure was measured by the same physician using a stethoscope (Spengler, Germany) and sphygmomanometer (Spengler, Germany).
Blood pressure and blood glucose were measured 1 hour after RB supplementation (correspond to pre-training session) and also immediately following the training session to assess any exercise effect on blood pressure/glucose responses during RB condition
Change in Blood pressure and blood glucose from pre- to post-training session using PL condition
Blood glucose was measured using the electrochemical sensor Rightest GM260 Blood Glucose Monitoring System (Bionime Corporation, Taichung City, Taiwan). The finger tip was pricked with a lancing device, and a specific test strip was soaked with blood was inserted into the measuring apparatus, with an estimate appearing within 5 seconds. Blood pressure was measured by the same physician using a stethoscope (Spengler, Germany) and sphygmomanometer (Spengler, Germany).
Blood pressure and blood glucose were measured 1 hour after PL supplementation (correspond to pre-training session) and also immediately following the training session to assess any exercise effect on blood pressure/glucose responses during PL condition
Change in hematological parameters from pre- to post-training session using RB condition
Haematological parameters (i.e., white blood cells (WBC), neutrophils (NEU), red blood cells (RBC), hemoglobin (HGB), hematocrit (HCT)and platelets (PLT) were determined using a multichannel automated blood cell analyser Beckman Coulter Gen system-2 (Coulter T540)
Hematological parameters were measured 1 hour after RB supplementation (correspond to pre-training session) and also immediately following the training session to assess any exercise effect on hematological responses during RB condition
Change in hematological parameters from pre to post training session using PL condition
Haematological parameters (i.e., white blood cells (WBC), neutrophils (NEU), red blood cells (RBC), hemoglobin (HGB), hematocrit (HCT)and platelets (PLT) were determined using a multichannel automated blood cell analyser Beckman Coulter Gen system-2 (Coulter T540)
Hematological parameters were measured 1 hour after PL supplementation (correspond to pre-training session) and also immediately following the training session to assess any exercise effect on hematological responses during PL condition
Change in muscle damage parameters from pre to post training session using RB condition
muscle damage markers: Creatinine kinase (CK), Alkaline phosphate (PAL), Gammaglutamyl (GGT), Lactate dehydrogenase (LDH), and c-reactive protein (CRP) were determined spectrophotometrically using Abott Architect Ci 4100.
Muscle damage parameters were measured 1 hour after RB supplementation (correspond to pre-training session) and also immediately following the training session to assess any exercise effect on muscle damage responses during RB condition
Change in muscle damage parameters from pre to post training session using PL condition
muscle damage markers: Creatinine kinase (CK), Alkaline phosphate (PAL), Gammaglutamyl (GGT), Lactate dehydrogenase (LDH), and c-reactive protein (CRP) were determined spectrophotometrically using Abott Architect Ci 4100.
Muscle damage parameters were measured 1 hour after PL supplementation (correspond to pre-training session) and also immediately following the training session to assess any exercise effect on muscle damage responses during PL condition
Change in oxidative stress parameters from pre to post training session using RB condition
Oxididative stress response (i.e., malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidase (GPx), Catalase (CAT), uric acid (UA)) and c-reactive protein (CRP)) were determined spectrophotometrically using Abott Architect Ci 4100.
Oxidative stress parameters were measured 1 hour after RB supplementation (correspond to pre-training session) and also immediately following the training session to assess any exercise effect on oxidative stress responses during RB condition
Change in oxidative stress parameters from pre to post training session using PL condition
Oxididative stress response (i.e., malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidase (GPx), Catalase (CAT), uric acid (UA)) and c-reactive protein (CRP)) were determined spectrophotometrically using Abott Architect Ci 4100.
Oxidative stress parameters were measured 1 hour after PL supplementation (correspond to pre-training session) and also immediately following the training session to assess any exercise effect on oxidative stress responses during PL condition
Study Arms (2)
Red Bull drink (RB)
EXPERIMENTALOver the study, three participants were unable to complete all test sessions due to muscle pain or injury . Thus, 19 participants (age: 21.2±1.2 years; height: 1.76±0.8 m; body-mass: 76.6±12.6 kg) completed all test sessions
Placebo drink
PLACEBO COMPARATOR19 participants (age: 21.2±1.2 years; height: 1.76±0.8 m; body-mass: 76.6±12.6 kg)
Interventions
Each participant visited the laboratory for two formal test sessions, drinking a caffeine-containing ED (RB) and a caffeine and taurine free beverage drink (PL). All sessions were arranged in the early evening hours to avoid any time of day effects. The two definitive test sessions were separated by an interval of seven days to allow sufficient recovery between tests and to ensure caffeine washout. To avoid identification, two opaque and unmarked cans of RB or PL were ingested by each participant (i.e., 500 mL) in the presence of a researcher. The two drinks were similar in volume, texture, and appearance. One can of RB drink (i.e., 250ml) contained 80 mg of caffeine, 1 g of taurine, 27 g of carbohydrates, 0.6 g of protein, 5 mg vitamin B6 and 487 kJ of energy.
The PL drink was prepared by an agri-food engineer; it did not contain any caffeine or taurine, but comprised carbonated water, carbohydrates, citric acid lemon juice reconstituted from concentrate (1 %), supplemented by flavorings, of sodium citrate, acesulfame K, sucralose, potassium sorbate and RB (a flavoring that contains propylene glycol E1520 (0.23 mL).
Eligibility Criteria
You may qualify if:
- years of age,
- BMI less than 25 kg/m2,
- low (\<1.5g/month \[20\]) caffeine users
- not regular caffeine users.
You may not qualify if:
- chronic metabolic disease such as type 2 diabetes and cardiovascular disease
- auto-immune disease such as rheumatoid arthritis, lupus or type 1 diabetes,
- liver disease
- intake of any medications/ or dietary supplements known to influence blood glucose and/or blood pressures.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- To avoid identification, two opaque and unmarked cans \[24-26\] of Red Bull or Placebo were ingested by each participant (i.e., 500 mL) in the presence of a researcher.
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 24, 2019
First Posted
May 3, 2019
Study Start
January 1, 2017
Primary Completion
January 12, 2017
Study Completion
January 12, 2017
Last Updated
May 3, 2019
Record last verified: 2019-05
Data Sharing
- IPD Sharing
- Will not share