Effect of 8-week Intake of 2S-hesperidin on Performance, Body Composition and Biochemicals Markers in Amateur Cyclists (HESPERFORMAN)
Primary Purpose
Power, Metabolic Disturbance, Change, Body Weight
Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
2S-hesperidin
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Power focused on measuring Flavonoids, Polyphenols, Power, Endurance sports, Ergogenic aids, Inflammatory markers, Antioxidant markers, Body Composition, Ventilatory Thresholds, Nutrigenomic
Eligibility Criteria
Inclusion Criteria:
- 18-55 years,
- BMI of 19-25.5 kg·m-2
- At least 3 years of cycling experience and training for 6-12 h·wk-1
Exclusion Criteria:
- Were smokers or regular alcohol drinkers,
- Had a metabolic, cardiorespiratory or digestive pathology or anomaly,
- Had an injury in the prior 6 months
- Were supplementing or medicating in the prior 2 weeks
- Had non-normal values in the blood analysis parameters.
Sites / Locations
- Research Center for High Performance Sport. Catholic University of Murcia
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
2S-hesperidin
Placebo
Arm Description
This group took 500 mg (capsules) per day at breakfast of 2S-hesperidin (Cardiose®) for 8 weeks
This group took 500 mg of microcellulose (capsules) per day at breakfast for 8 weeks
Outcomes
Primary Outcome Measures
Maximum power
During the incremental test until exhaustion, the power generated was measured maximum power (W)
Power generated at FatMax
During the incremental test until exhaustion, the power generated was measured in FatMax (W)
Power generated at ventilatory threshold 1 (VT1)
During the incremental test until exhaustion, the power generated was measured in VT1 (W)
Power generated at ventilatory threshold 2 (VT2)
During the incremental test until exhaustion, the power generated was measured in VT2 (W)
Secondary Outcome Measures
Fat mass
Fat mass (g) was measured by densitometry and anthropometry.
Sum of 8 skinfolds
By means of anthropometry, the sum of 8 skinfolds (mm) was calculated.
Muscle mass
Muscle mass (g) was measured by densitometry and anthropometry
Resting metabolic rate
Resting metabolic rate was measured by indirect calorimetry.
Superoxide dismutase (antioxidant marker)
During the rectangular test, superoxide dismutase (U/g Hb) was measured in venous blood.
Catalase (antioxidant marker)
During the rectangular test, catalase (U/g Hb) was measured in venous blood.
Reduced glutathione (antioxidant marker)
During the rectangular test, reduced glutathione (GSH) (nmol/mg protein) was measured in venous blood.
Oxidized glutathione (antioxidant marker)
During the rectangular test, oxidized glutathione (GSSG) (nmol/mg protein) was measured in venous blood.
GSSG/GSH ratio (antioxidant marker)
During the rectangular test, GSSG/GSH ratio (%) was measured in venous blood.
Hemoxigenase 1 (antioxidant marker)
During the rectangular test, hemoxigenase 1 (ng/mL) was measured in venous blood.
Thiobarbituric acid reactive substances (oxidant marker)
During the rectangular test, thiobarbituric acid reactive substances (TBARS) (mcm/L) ( are formed as a byproduct of lipid peroxidation) was measured to determine the oxidative state in venous blood.
Interleukin 6 (inflammatory marker)
During the rectangular test, interleukin 6 (pg/ml) was measured in venous blood.
Tumor necrosis factor (inflammatory marker)
During the rectangular test, tumor necrosis (pg/ml) was measured in venous blood.
C-reactive protein (inflammatory marker)
During the rectangular test, C-reactive protein (mg/L) was measured in venous blood.
Monocyte chemoattractant protein-1 (inflammatory marker)
During the rectangular test, monocyte chemoattractant protein-1 (pg/ml) was measured in venous blood.
Hemoglobin (oximetry marker)
During the rectangular test, hemoglobin (g/dL) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Hematocrit (oximetry marker)
During the rectangular test, hematocrit (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Oxygen saturation (oximetry marker)
During the rectangular test, oxygen saturation (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Oxygen partial pressure (oximetry marker)
During the rectangular test, oxygen partial pressure (mmHg) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Carbon dioxide partial pressure (oximetry marker)
During the rectangular test, carbon dioxide partial pressure (mmHg) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Oxyhemoglobin (oximetry marker)
During the rectangular test, oxyhemoglobin (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Carboxyhemoglobin (oximetry marker)
During the rectangular test, carboxyhemoglobin (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Deoxyhemoglobin (oximetry marker)
During the rectangular test, deoxyhemoglobin (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Methemoglobin (oximetry marker)
During the rectangular test, methemoglobin (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Total blood oxygen concentration (oximetry marker)
During the rectangular test, total blood oxygen concentration (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Total blood carbon dioxide concentration (oximetry marker)
During the rectangular test, total blood carbon dioxide concentration (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Oxygen partial pressure at 50% oxygen saturation (oximetry marker)
During the rectangular test, oxygen partial pressure at 50% oxygen saturation (mmHg) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Relative physiological Shunt (oximetry marker)
During the rectangular test, relative physiological Shunt (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Alveolar-arterial gradient (oximetry marker)
During the rectangular test, alveolar-arterial gradient (mmHg) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Bicarbonate (metabolic marker)
During the rectangular test, bicarbonate (mmol/L) wasa measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Glucose (metabolic marker)
During the rectangular test, glucose (mg/dL) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Lactate (metabolic marker)
During the rectangular test, lactate (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
pH (metabolic marker)
During the rectangular test, pH was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Actual base excess (metabolic marker)
During the rectangular test, actual base excess (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Standard base excess (metabolic marker)
During the rectangular test, standard base excess (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Sodium (metabolic marker)
During the rectangular test, sodium (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Potassium (metabolic marker)
During the rectangular test, potassium (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Chloride (metabolic marker)
During the rectangular test, chloride (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Calcium (metabolic marker)
During the rectangular test, calcium (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Full Information
NCT ID
NCT04597983
First Posted
September 30, 2020
Last Updated
October 21, 2020
Sponsor
Francisco Javier Martínez Noguera
1. Study Identification
Unique Protocol Identification Number
NCT04597983
Brief Title
Effect of 8-week Intake of 2S-hesperidin on Performance, Body Composition and Biochemicals Markers in Amateur Cyclists
Acronym
HESPERFORMAN
Official Title
Effect of 8-week Intake of 2S-hesperidin on Performance, Body Composition and Biochemicals Markers in Amateur Cyclists
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
September 22, 2018 (Actual)
Primary Completion Date
December 21, 2018 (Actual)
Study Completion Date
December 21, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Francisco Javier Martínez Noguera
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This clinical study evaluates the effect of 500 mg of 2S-hesperidin for 8 weeks on performance (power generated in different metabolic zones), body composition (fat and muscle mass) and biochemical (antioxidant, inflammatory status) and metabolic (capillary blood in finger) markers in amateur cyclists. Our hypothesis is that chronic intake of 2S-hesperidin can improve performance (maximum power generated). To justify this hypothesis, we measured the parameters mentioned above, which could establish a cause-effect relationship between 2S-hesperidin intake and possible yield improvement.
Detailed Description
Participants
All participants were informed about the procedures and provided signed informed consent. The study was conducted according to the guidelines of the Helsinki Declaration for Human Research and the protocol was approved by the Ethics Committee/Institutional Review Catholic University of Murcia (Code: CE091802).
Study design
Cyclists were instructed to take the supplement along with breakfast and to continue their usual diet and training schedule. Subjects in both groups were instructed not to consume foods high in citrus flavonoids (grapefruit, lemons or oranges) for 5 days prior to and during the study, this was verified by diet recalls records.
Procedures
Participants visited the laboratory on seven occasions. Visit 1 consisted of a medical examination and blood extraction to determine health status. On visits 2 and 5, a 24-hr diet recall and a Wingate test were performed. On visits 3 and 6, another 24-hour diet recall was conducted, followed by an incremental test until exhaustion on a cycle ergometer. On visits 4 and 7, the 24-hour diet recall was repeated, and participants performed a rectangular test on the cycle ergometer. Prior to each testing session (visits 2, 3, 4, 5, 6 and 7), a standardized breakfast composed of 95.16 g of carbohydrates (68%), 18.86 g of protein (14%) and 11.30 g of lipids (18%) was prescribed by the sport nutritionist.
Pre and post evaluation test
Pre-intervention visits: 1,2,3 and 4 Post-intervention visits: 5,6 and 7
Visit 1:
Health status blood analysis: A general analysis will be performed both in the pre and post-supplementation period. The extraction will be done by venous via. (Fasting)
Medical examination: A clinical history of family and personal history, a resting electrocardiogram (ECG) and a medical examination (auscultation, blood pressure measurement, etc.) will be taken to certify that the person is healthy and not at risk to participate in the study. (Fasting)
Visits 2 and 5:
Resting Metabolic Rate (RMR): A resting test will be performed with the ergospirometer to determine macronutrient supply at rest and caloric expenditure. (Fasting)
Body composition by absorptiometric densitometry (DXA): A body composition test will be performed by the dual energy absorptiometric densitometry technique (X-ray), with the objective of to determine parameters of fat mass, fat-free mass and fat percentage. In addition, anthropometry was also used to determine changes in body composition (fat and muscle mass). (Fasting)
Anaerobic power and mechanical power production: After a standardized breakfast, a Wingate test was performed on a cycloergometer. Wingate test (WAnT) consisted of an all-out 30-s sprint on a cycloergometer (Monark Ergomedic 894E Peak Bike, Vansbro, Sweden). Breaking resistance was held constant at 7.5% of each individual's body mass. All participants were verbally encouraged to pedal as fast as possible during the entire sprint.
Visits 3 and 6:
Incremental step with final ramp test was performed on a cycle ergometer using a metabolic cart (Metalyzer 3B. Leipzig, Germany) to determine maximal fat oxidation zone (FatMax), ventilatory thresholds 1 (VT1) and 2 (VT2) and maximal oxygen consumption (VO2max). Participants began cycling at 35W for 2 min, increasing then by 35W every 2 min until RER>1.05, initialling then the final ramp (+35W·min-1) until exhaustion. The estimated functional threshold power (FTP) was calculated using the following equation [16]:
FTP (W) = Pmax (W) x 0.865 - 56.484.
Visits 4 and 7:
Rectangular test was performed on a cycle ergometer using the power output values resulting from the maximal test (FatMax, VT1 and VT2). Participants exercised continuously from FatMax, to VT1 and to VT2 for 10 min, without rest. Cardiorespiratory variables (VO2, VO2R, carbohydrate oxidation (CHO), fat oxidation (FAT) and cycling economy) were determined for each metabolic zones.
Urine samples
Main hesperidin metabolites were analysed in participants' urine. Urine samples, corresponding to 24 h urine collection from each participant before and after the supplementation, were frozen in liquid nitrogen after collection and thawed for its analysis.
All the data of the subjects who participated in the study were stored under a computer system with a security key. In addition, a record was also made of some of the paper data that was saved under key, and to which only the researchers of this project had access.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Power, Metabolic Disturbance, Change, Body Weight, Changes Fatty, Muscle Loss, Oxidative Stress, Inflammatory Response, Oxygen Deficiency, Acid-Base Imbalance, Electrolyte Disturbance
Keywords
Flavonoids, Polyphenols, Power, Endurance sports, Ergogenic aids, Inflammatory markers, Antioxidant markers, Body Composition, Ventilatory Thresholds, Nutrigenomic
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A randomized parallel study was conducted, where 40 amateur cyclists were divided into 2 groups: one group took 500 mg of 2S-hesperidin (n= 20) and the other group took 500 mg of placebo (microcellulose) (n= 20). All participants completed the study.
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
The company that performed the encapsulation of both the 2S-hesperidin and the placebo performed the randomization, therefore no one on the research team or the sponsors knew which group each study subject belonged to. The results of the randomization were sent to our laboratory after the end of the study to determine which subjects composed each group
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
2S-hesperidin
Arm Type
Experimental
Arm Description
This group took 500 mg (capsules) per day at breakfast of 2S-hesperidin (Cardiose®) for 8 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
This group took 500 mg of microcellulose (capsules) per day at breakfast for 8 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
2S-hesperidin
Other Intervention Name(s)
Cardiose®
Intervention Description
Cardiose® is a natural orange extract that due to its unique manufacturing process, maintains most of the natural hesperidin isomeric form (2S)
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Other Intervention Name(s)
Microcellulose
Intervention Description
Microcellulose was used, this molecule was selected to avoid affecting the glycemia, as it can occur with dextrose or maltodextrin.
Primary Outcome Measure Information:
Title
Maximum power
Description
During the incremental test until exhaustion, the power generated was measured maximum power (W)
Time Frame
Throughout study completion, an average of 8 weeks
Title
Power generated at FatMax
Description
During the incremental test until exhaustion, the power generated was measured in FatMax (W)
Time Frame
Throughout study completion, an average of 8 weeks
Title
Power generated at ventilatory threshold 1 (VT1)
Description
During the incremental test until exhaustion, the power generated was measured in VT1 (W)
Time Frame
Throughout study completion, an average of 8 weeks
Title
Power generated at ventilatory threshold 2 (VT2)
Description
During the incremental test until exhaustion, the power generated was measured in VT2 (W)
Time Frame
Throughout study completion, an average of 8 weeks
Secondary Outcome Measure Information:
Title
Fat mass
Description
Fat mass (g) was measured by densitometry and anthropometry.
Time Frame
Throughout study completion, an average of 8 weeks
Title
Sum of 8 skinfolds
Description
By means of anthropometry, the sum of 8 skinfolds (mm) was calculated.
Time Frame
Throughout study completion, an average of 8 weeks
Title
Muscle mass
Description
Muscle mass (g) was measured by densitometry and anthropometry
Time Frame
Throughout study completion, an average of 8 weeks
Title
Resting metabolic rate
Description
Resting metabolic rate was measured by indirect calorimetry.
Time Frame
Throughout study completion, an average of 8 weeks
Title
Superoxide dismutase (antioxidant marker)
Description
During the rectangular test, superoxide dismutase (U/g Hb) was measured in venous blood.
Time Frame
Superoxide dismutase was measured in pre, after the maximum power phase of the rectangular test and after the recovery phase in pre and post intervention (8 weeks) in both groups.
Title
Catalase (antioxidant marker)
Description
During the rectangular test, catalase (U/g Hb) was measured in venous blood.
Time Frame
Catalase was measured in pre, after the maximum power phase of the rectangular test and after the recovery phase in pre and post intervention (8 weeks) in both groups.
Title
Reduced glutathione (antioxidant marker)
Description
During the rectangular test, reduced glutathione (GSH) (nmol/mg protein) was measured in venous blood.
Time Frame
Reduced glutathione was measured in pre, after the maximum power phase of the rectangular test and after the recovery phase in pre and post intervention (8 weeks) in both groups.
Title
Oxidized glutathione (antioxidant marker)
Description
During the rectangular test, oxidized glutathione (GSSG) (nmol/mg protein) was measured in venous blood.
Time Frame
Oxidized glutathione was measured in pre, after the maximum power phase of the rectangular test and after the recovery phase in pre and post intervention (8 weeks) in both groups.
Title
GSSG/GSH ratio (antioxidant marker)
Description
During the rectangular test, GSSG/GSH ratio (%) was measured in venous blood.
Time Frame
GSSG/GSH ratio was measured in pre, after the maximum power phase of the rectangular test and after the recovery phase in pre and post intervention (8 weeks) in both groups.
Title
Hemoxigenase 1 (antioxidant marker)
Description
During the rectangular test, hemoxigenase 1 (ng/mL) was measured in venous blood.
Time Frame
Hemoxigenase 1 was measured in pre, after the maximum power phase of the rectangular test and after the recovery phase in pre and post intervention (8 weeks) in both groups.
Title
Thiobarbituric acid reactive substances (oxidant marker)
Description
During the rectangular test, thiobarbituric acid reactive substances (TBARS) (mcm/L) ( are formed as a byproduct of lipid peroxidation) was measured to determine the oxidative state in venous blood.
Time Frame
Thiobarbituric acid reactive substances was measured in pre, after the maximum power phase of the rectangular test and after the recovery phase in pre and post intervention (8 weeks) in both groups.
Title
Interleukin 6 (inflammatory marker)
Description
During the rectangular test, interleukin 6 (pg/ml) was measured in venous blood.
Time Frame
Interleukin 6 was measured in pre, after the maximum power phase of the rectangular test and after the recovery phase in pre and post intervention (8 weeks) in both groups.
Title
Tumor necrosis factor (inflammatory marker)
Description
During the rectangular test, tumor necrosis (pg/ml) was measured in venous blood.
Time Frame
Tumor necrosis factor was measured in pre, after the maximum power phase of the rectangular test and after the recovery phase in pre and post intervention (8 weeks) in both groups.
Title
C-reactive protein (inflammatory marker)
Description
During the rectangular test, C-reactive protein (mg/L) was measured in venous blood.
Time Frame
C-reactive protein was measured in pre, after the maximum power phase of the rectangular test and after the recovery phase in pre and post intervention (8 weeks) in both groups.
Title
Monocyte chemoattractant protein-1 (inflammatory marker)
Description
During the rectangular test, monocyte chemoattractant protein-1 (pg/ml) was measured in venous blood.
Time Frame
Monocyte chemoattractant protein-1 was measured in pre, after the maximum power phase of the rectangular test and after the recovery phase in pre and post intervention (8 weeks) in both groups.
Title
Hemoglobin (oximetry marker)
Description
During the rectangular test, hemoglobin (g/dL) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Hemoglobin was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Hematocrit (oximetry marker)
Description
During the rectangular test, hematocrit (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Hematocrit was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Oxygen saturation (oximetry marker)
Description
During the rectangular test, oxygen saturation (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Oxygen saturation was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Oxygen partial pressure (oximetry marker)
Description
During the rectangular test, oxygen partial pressure (mmHg) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Oxygen partial pressure was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Carbon dioxide partial pressure (oximetry marker)
Description
During the rectangular test, carbon dioxide partial pressure (mmHg) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Carbon dioxide partial pressure was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Oxyhemoglobin (oximetry marker)
Description
During the rectangular test, oxyhemoglobin (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Oxyhemoglobin was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Carboxyhemoglobin (oximetry marker)
Description
During the rectangular test, carboxyhemoglobin (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Carboxyhemoglobin was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Deoxyhemoglobin (oximetry marker)
Description
During the rectangular test, deoxyhemoglobin (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Deoxyhemoglobin was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Methemoglobin (oximetry marker)
Description
During the rectangular test, methemoglobin (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Methemoglobin was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Total blood oxygen concentration (oximetry marker)
Description
During the rectangular test, total blood oxygen concentration (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Total blood oxygen concentration was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Total blood carbon dioxide concentration (oximetry marker)
Description
During the rectangular test, total blood carbon dioxide concentration (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Total blood carbon dioxide concentration was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Oxygen partial pressure at 50% oxygen saturation (oximetry marker)
Description
During the rectangular test, oxygen partial pressure at 50% oxygen saturation (mmHg) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Oxygen partial pressure at 50% oxygen saturation was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Relative physiological Shunt (oximetry marker)
Description
During the rectangular test, relative physiological Shunt (%) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Relative physiological Shunt was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Alveolar-arterial gradient (oximetry marker)
Description
During the rectangular test, alveolar-arterial gradient (mmHg) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Alveolar-arterial gradient was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Bicarbonate (metabolic marker)
Description
During the rectangular test, bicarbonate (mmol/L) wasa measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Bicarbonate was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Glucose (metabolic marker)
Description
During the rectangular test, glucose (mg/dL) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Glucose was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Lactate (metabolic marker)
Description
During the rectangular test, lactate (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Lactate was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
pH (metabolic marker)
Description
During the rectangular test, pH was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
pH was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Actual base excess (metabolic marker)
Description
During the rectangular test, actual base excess (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Actual base excess was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Standard base excess (metabolic marker)
Description
During the rectangular test, standard base excess (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Standard base excess was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Sodium (metabolic marker)
Description
During the rectangular test, sodium (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Sodium was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Potassium (metabolic marker)
Description
During the rectangular test, potassium (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Potassium was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Chloride (metabolic marker)
Description
During the rectangular test, chloride (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Chloride was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
Title
Calcium (metabolic marker)
Description
During the rectangular test, calcium (mmol/L) was measured using capillary blood obtained from a finger prick and analyzed in a blood gas analyzer (ABL90 FLEX PLUS, Radiometer Iberica, Spain)
Time Frame
Calcium was analyzed pre, at the end of the FatMax phase, VT1, VT2, maximum power, FatMax2 and after the recovery phase of the rectangular test in pre and post intervention (8 weeks) in both groups.)
10. Eligibility
Sex
Male
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
18-55 years,
BMI of 19-25.5 kg·m-2
At least 3 years of cycling experience and training for 6-12 h·wk-1
Exclusion Criteria:
Were smokers or regular alcohol drinkers,
Had a metabolic, cardiorespiratory or digestive pathology or anomaly,
Had an injury in the prior 6 months
Were supplementing or medicating in the prior 2 weeks
Had non-normal values in the blood analysis parameters.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pedro Emilio Alcaraz Ramón
Organizational Affiliation
Catholic University of Murcia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Research Center for High Performance Sport. Catholic University of Murcia
City
La Ñora
State/Province
Murcia
ZIP/Postal Code
30830
Country
Spain
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effect of 8-week Intake of 2S-hesperidin on Performance, Body Composition and Biochemicals Markers in Amateur Cyclists
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