Ignite Creation Date:
2024-05-06 @ 5:48 PM
Last Modification Date:
2024-10-26 @ 2:36 PM
Study NCT ID:
NCT05439239
Status:
UNKNOWN
Last Update Posted:
2022-06-30
First Post:
2022-05-31
Brief Title:
Effects of Hypoxic Repeated Sprint Training on Performance in Normoxia in Male and Female Athletes
Sponsor:
Université Catholique de Louvain
Organization:
Université Catholique de Louvain
Study Overview
Official Title:
Effects of Hypoxic Repeated Sprint Training on Performance in Normoxia in Male and Female Athletes Participating in TeamRacket Sports
Status:
UNKNOWN
Status Verified Date:
2022-06
Last Known Status:
RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
RSHwomen
Brief Summary:
With the increased participation of women in sports it is essential to develop gender-tailored training strategies for improving exercise performance Males and females exhibit gender-specific characteristics and they therefore respond differently to physical exercise Improving repeated sprint ability RSA ie ability to perform repeated short duration sprints separated by brief recovery intervals in women is important for sports performance as it is a key factor in most team and racket sports Repeated sprint training in hypoxia is increasingly popular in this field as it has demonstrated further improvements in sea-level repeated sprint performance than similar training in normoxia However these observations are based mainly on male athletes Whether the effects of hypoxic repeated sprint training on repeated sprint performance in normoxia differ between genders is not yet known therefore the investigators propose to examine those possible differences in this study
The aim of this study is to investigate whether the effects of hypoxic repeated sprint training on repeated sprint performance in normoxia differ between males and females who participate in teamracket sports
Considering the sex-specific characteristics that males and females exhibit the investigators hypothesize that after 7 weeks of hypoxic repeated sprint training the improvements in repeated sprint ability at sea level will be greater in males than in females
To answer this question the investigators will measure the following body composition lean body mass body weight and height VO2max blood estrogen lactate hemoglobin hematocrit repeated sprint ability RSA test muscle oxygenation concentrations for oxyhemoglobin deoxyhemoglobin and total hemoglobinmyoglobin 30-s Wingate test heart rate HR power output rate of perceived exertion RPE visual analogue scale VAS pain level in legs
The investigators will recruit 48 volunteers and they will randomly assign them into the normoxic or hypoxic training group without giving any information about their group The volunteers should meet the following inclusion criteria females on monophasic oral contraceptive pill and males age between 18-40 years recreationally participating in teamracket sports min 3hweek with at least 2 years of experience prior to the study Exclusion criteria will be smoking exposure to altitude 1500 m one month before the study any health conditions or injuries that could compromise the participants safety during trainingtesting prescribed medication performing repeated sprint training more than once per week
Males and females matched for VO2max and sprint performance will perform repeated sprint training 3 sets during week 1-6 2 sets during week 7 with 5min active recovery in between 5 x 10s maximal sprints with 20s active recovery in between in hypoxia or normoxia 2xweek for 7 weeks Before and after the training period the following tests and measurements will be performed body composition analysis VO2max test blood sampling for measuring hemoglobin and estrogen concentrations and hematocrit determination of hemoglobin mass RSA test muscle oxygenation assessment during RSA test 30-s Wingate test and blood lactate measurements
The aim of this study is to investigate whether the effects of hypoxic repeated sprint training on repeated sprint performance in normoxia differ between males and females who participate in teamracket sports
Considering the sex-specific characteristics that males and females exhibit the investigators hypothesize that after 7 weeks of hypoxic repeated sprint training the improvements in repeated sprint ability at sea level will be greater in males than in females
To answer this question the investigators will measure the following body composition lean body mass body weight and height VO2max blood estrogen lactate hemoglobin hematocrit repeated sprint ability RSA test muscle oxygenation concentrations for oxyhemoglobin deoxyhemoglobin and total hemoglobinmyoglobin 30-s Wingate test heart rate HR power output rate of perceived exertion RPE visual analogue scale VAS pain level in legs
The investigators will recruit 48 volunteers and they will randomly assign them into the normoxic or hypoxic training group without giving any information about their group The volunteers should meet the following inclusion criteria females on monophasic oral contraceptive pill and males age between 18-40 years recreationally participating in teamracket sports min 3hweek with at least 2 years of experience prior to the study Exclusion criteria will be smoking exposure to altitude 1500 m one month before the study any health conditions or injuries that could compromise the participants safety during trainingtesting prescribed medication performing repeated sprint training more than once per week
Males and females matched for VO2max and sprint performance will perform repeated sprint training 3 sets during week 1-6 2 sets during week 7 with 5min active recovery in between 5 x 10s maximal sprints with 20s active recovery in between in hypoxia or normoxia 2xweek for 7 weeks Before and after the training period the following tests and measurements will be performed body composition analysis VO2max test blood sampling for measuring hemoglobin and estrogen concentrations and hematocrit determination of hemoglobin mass RSA test muscle oxygenation assessment during RSA test 30-s Wingate test and blood lactate measurements
Detailed Description:
A single blind parallel gender comparative randomized controlled trial design will be used and the methodology of this study will be based on a previously applied successful protocol on males Participants males and females will be randomly assigned to either the control group repeated sprint training in normoxia RSN or the intervention group repeated sprint training group in hypoxia RSH resulting in four groups in total females RSN and RSH males RSN and RSH Due to the big number of participants required the experiment will be split into two studies RSN will be performed in study 1 and RSH in study 2 The experiment involves 7 weeks week 1-7 of cycling repeated sprint training in normoxia or hypoxia 2xweek and two testing sessions before week -2-1 Pre-testing and after week 89 Post-testing the training period During the testing sessions participants will complete the following exercise performance tests and measurements in normoxia body composition assessment through DEXA dual energy x-ray absorptiometry and skinfold measurements VO2max test blood sampling at rest to measure hemoglobin and estrogen concentrations and hematocrit determination of hemoglobin mass repeated sprint ability RSA test and near-infrared spectroscopy NIRS measurement for muscle oxygenation and 30-s Wingate test Blood lactate will be measured at rest before and immediately after the following exercise performance tests RSA and Wingate
Preliminary visit
During the week before Pre-testing participants will be assessed for eligibility through a medical screening and completion of questionnaires medical screening and physical activitylifestyle questionnaires after signing the informed consent related to the Pre-screening If they are eligible and still wish to take part to the study participants will sign the informed consent related to the study and they will get familiarized with all the experimental procedures
Supervised training
Participants will perform 7 weeks of cycling repeated sprint training 2xweek starting the week after the Pre- testing and finishing the week before the Post-testing The training sessions will take place in a hypoxic chamber consisting of a compressor built in the laboratory Inspired oxygen fraction FiO2 will be set to 146 and 209 for RSH and RSN to simulate an altitude of 3000 m and 300 m respectively In order to blind subjects to altitude the compressor system will also be running for RSN but with a normoxic airflow into the chamber Temperature in the chamber will be maintained constant throughout the training program
The training sessions will consist of a 10-min warm up at 50 of the VO2max of each participant followed by 3 sets of 5 x 10-s all-out repeated sprints on the cycle ergometer The number of sets will decrease to two during week 7 Participants will be instructed to try to reach and maintain maximal power output during each sprint An active recovery at 30 of VO2max will be allowed for 20 s between sprints and for 5 min between sets The training will end with a 10-min cool down at 30 VO2max An individual fixed torque of 07 Nmkg will be used during the sprints and it will be reduced to 05 Nmkg at week 7 Power output and heart rate will be recorded during each training session Water will be provided to all participants to ensure appropriate hydration during training After each session participants will be asked to report their rate of perceived exertion RPE Borg Scale 6-20 and the level of pain in the legs continuous visual analogic scale VAS At least one day of rest will be allowed between the two weekly sessions to ensure optimal recovery Participants will be asked to maintain their usual training outside the laboratory and fill a training diary
Pre- and Post- testing
Each pre- and post- testing session consists of two days Participants will be asked to complete a food diary during the three days prior to each test session and reproduce their diet as much as possible They will also be instructed to refrain from alcohol and caffeine intake during the 24 h before each test and from heavy exercise during the 48 h before Participants will be advised to consume a standard meal before the tests During the tests tap water will be provided ad libitum to all participants
During testing day 1 body weight and height will be measured and body composition will be assessed using DEXA dual energy x-ray absorptiometry scan and skinfold measurements A blood sample will be taken at rest from the antecubital vein for measuring hemoglobin and estrogen concentrations and hematocrit Estrogen levels will also be assessed to ensure that female participants are not ovulating despite the pill on the test days Participants will then perform a maximal incremental exercise test to assess aerobic performance VO2max One hour after the test hemoglobin mass will be determined according to the CO rebreathing method
During testing day 2 participants will perform an RSA test and a Wingate test Blood lactate concentration will be measured from an earlobe sample of 5ul at rest before each test and then immediately after and at 2 4 and 6 minutes after the exercise performance tests ie RSA and Wingate tests
For all performance tests the participants will use the cycle ergometer The seat and handlebar positions will be adjusted for each participant and reproduced for all tests During the RSA and Wingate tests the investigators will record heart rate peak and average power output and pedaling frequency After each test participants will be asked to report their RPE and VAS
Pre- and Post- testing will be performed in the exact same order in normoxia in the well-ventilated laboratory at a constant temperature of 18 o C
VO2max test
After blood sampling on day 1 participants will perform a VO2max test The starting load for the test will be set at 12 Wkg LBM and will be incremented by 06 Wkg LBM every 2 min until exhaustion Oxygen consumption and carbon dioxide production will be measured throughout the test using a gas exchange analyser and maximum oxygen consumption VO2max will be determined Heart rate will also be recorded during the test Upon completion of the test participants will be asked to report their RPE and VAS
Repeated Sprint Ability Test
During testing day 2 participants will arrive at the laboratory and a baseline measurement 3min of muscle oxygenation of the right vastus lateralis will be taken in a seated position using the NIRS method Then participants will perform a 10-min warm-up at 50 of their VO2max including two 5-s all-out sprints against a fixed torque of 08 Nmkg Following the warm-up another NIRS measurement will be taken at rest Participants will then start pedaling for 20 s at 30 VO2max before performing the RSA test The test consists of 10-s all-out sprints against a fixed torque of 08 Nmkg with a 20-s active recovery after each sprint at 30 VO2max Participants will be instructed to try to reach and maintain maximal power output during each sprint of the test They will also be given strong verbal encouragement and will be instructed to perform as many sprints as possible until volitional exhaustion No indication on the number of sprints performed will be given A minimal pedaling frequency of 70 rpm for more than 5 s during a sprint will be a criterion to stop the test Upon completion of the test a 10-min cool down at 30 VO2max will follow
NIRS
Changes in muscle oxygenation will be measured during the RSA test by the NIRS technique using the difference in absorption characteristics of light between 760 and 850 nm Skinfold will be measured with a caliper in order to confirm that the distance between the NIRS apparatus and the muscle is not higher than 16 mm The apparatus will then be fixed on vastus lateralis of the right leg with a large bandage to avoid interference by extraneous light and loss of transmitted light out of the field of investigation
Concentrations for oxyhemoglobin O2Hb deoxyhemoglobin HHb and total hemoglobinmyoglobin tHb will be determined Amplitudes during the following sprints and the average value for all sprints throughout the RSA test ie ΔHHbav and ΔtHbav will be calculated The same analysis will be performed during the successive recovery phases In addition the ΔtHbPower will be calculated as the ratio between ΔtHb and mean power for each sprint as an index of blood perfusion relative to the intensity of each sprint
Hemoglobin mass measurement
For this measurement 7 blood samples of about 70ul will be taken at the fingertip 5 before CO inhalation and 2 after The CO-rebreathing method consists in the inhalation of a low quantity of CO 1mkg bw mixed with oxygen Having a high affinity for hemoglobin CO binds to the later preferentially To measure total hemoglobin mass the fraction of CO bound to hemoglobin ABL90 Flex Radiometer will be evaluated before and after the inhalation of the mixed gas oxygen CO as well as the CO concentration in the exhaled air CO-meter Dräger
30 s Wingate Test
One hour after the RSA test participants will perform a 10-min warm-up on the cycle ergometer at 30 of their VO2max including two 5-s sprints at a test load Then they will complete a 30-s maximal cycling exercise with a resistance set to 75 of the participants body weight 0075 kgkg bw The participants will be asked to try and generate the highest power possible throughout the test and will receive strong verbal encouragement A 10-min cool down will follow
The investigators will match the male and female participants as closely as possible for sprint performance recorded during the RSA test of Pre- testing The average power of the best two sprints will be calculated in Watts and then expressed as joules per kilogram of lean body mass LBM Moreover the investigators will match participants for VO2max relative to LBM recorded during the incremental test of Pre- testing
Preliminary visit
During the week before Pre-testing participants will be assessed for eligibility through a medical screening and completion of questionnaires medical screening and physical activitylifestyle questionnaires after signing the informed consent related to the Pre-screening If they are eligible and still wish to take part to the study participants will sign the informed consent related to the study and they will get familiarized with all the experimental procedures
Supervised training
Participants will perform 7 weeks of cycling repeated sprint training 2xweek starting the week after the Pre- testing and finishing the week before the Post-testing The training sessions will take place in a hypoxic chamber consisting of a compressor built in the laboratory Inspired oxygen fraction FiO2 will be set to 146 and 209 for RSH and RSN to simulate an altitude of 3000 m and 300 m respectively In order to blind subjects to altitude the compressor system will also be running for RSN but with a normoxic airflow into the chamber Temperature in the chamber will be maintained constant throughout the training program
The training sessions will consist of a 10-min warm up at 50 of the VO2max of each participant followed by 3 sets of 5 x 10-s all-out repeated sprints on the cycle ergometer The number of sets will decrease to two during week 7 Participants will be instructed to try to reach and maintain maximal power output during each sprint An active recovery at 30 of VO2max will be allowed for 20 s between sprints and for 5 min between sets The training will end with a 10-min cool down at 30 VO2max An individual fixed torque of 07 Nmkg will be used during the sprints and it will be reduced to 05 Nmkg at week 7 Power output and heart rate will be recorded during each training session Water will be provided to all participants to ensure appropriate hydration during training After each session participants will be asked to report their rate of perceived exertion RPE Borg Scale 6-20 and the level of pain in the legs continuous visual analogic scale VAS At least one day of rest will be allowed between the two weekly sessions to ensure optimal recovery Participants will be asked to maintain their usual training outside the laboratory and fill a training diary
Pre- and Post- testing
Each pre- and post- testing session consists of two days Participants will be asked to complete a food diary during the three days prior to each test session and reproduce their diet as much as possible They will also be instructed to refrain from alcohol and caffeine intake during the 24 h before each test and from heavy exercise during the 48 h before Participants will be advised to consume a standard meal before the tests During the tests tap water will be provided ad libitum to all participants
During testing day 1 body weight and height will be measured and body composition will be assessed using DEXA dual energy x-ray absorptiometry scan and skinfold measurements A blood sample will be taken at rest from the antecubital vein for measuring hemoglobin and estrogen concentrations and hematocrit Estrogen levels will also be assessed to ensure that female participants are not ovulating despite the pill on the test days Participants will then perform a maximal incremental exercise test to assess aerobic performance VO2max One hour after the test hemoglobin mass will be determined according to the CO rebreathing method
During testing day 2 participants will perform an RSA test and a Wingate test Blood lactate concentration will be measured from an earlobe sample of 5ul at rest before each test and then immediately after and at 2 4 and 6 minutes after the exercise performance tests ie RSA and Wingate tests
For all performance tests the participants will use the cycle ergometer The seat and handlebar positions will be adjusted for each participant and reproduced for all tests During the RSA and Wingate tests the investigators will record heart rate peak and average power output and pedaling frequency After each test participants will be asked to report their RPE and VAS
Pre- and Post- testing will be performed in the exact same order in normoxia in the well-ventilated laboratory at a constant temperature of 18 o C
VO2max test
After blood sampling on day 1 participants will perform a VO2max test The starting load for the test will be set at 12 Wkg LBM and will be incremented by 06 Wkg LBM every 2 min until exhaustion Oxygen consumption and carbon dioxide production will be measured throughout the test using a gas exchange analyser and maximum oxygen consumption VO2max will be determined Heart rate will also be recorded during the test Upon completion of the test participants will be asked to report their RPE and VAS
Repeated Sprint Ability Test
During testing day 2 participants will arrive at the laboratory and a baseline measurement 3min of muscle oxygenation of the right vastus lateralis will be taken in a seated position using the NIRS method Then participants will perform a 10-min warm-up at 50 of their VO2max including two 5-s all-out sprints against a fixed torque of 08 Nmkg Following the warm-up another NIRS measurement will be taken at rest Participants will then start pedaling for 20 s at 30 VO2max before performing the RSA test The test consists of 10-s all-out sprints against a fixed torque of 08 Nmkg with a 20-s active recovery after each sprint at 30 VO2max Participants will be instructed to try to reach and maintain maximal power output during each sprint of the test They will also be given strong verbal encouragement and will be instructed to perform as many sprints as possible until volitional exhaustion No indication on the number of sprints performed will be given A minimal pedaling frequency of 70 rpm for more than 5 s during a sprint will be a criterion to stop the test Upon completion of the test a 10-min cool down at 30 VO2max will follow
NIRS
Changes in muscle oxygenation will be measured during the RSA test by the NIRS technique using the difference in absorption characteristics of light between 760 and 850 nm Skinfold will be measured with a caliper in order to confirm that the distance between the NIRS apparatus and the muscle is not higher than 16 mm The apparatus will then be fixed on vastus lateralis of the right leg with a large bandage to avoid interference by extraneous light and loss of transmitted light out of the field of investigation
Concentrations for oxyhemoglobin O2Hb deoxyhemoglobin HHb and total hemoglobinmyoglobin tHb will be determined Amplitudes during the following sprints and the average value for all sprints throughout the RSA test ie ΔHHbav and ΔtHbav will be calculated The same analysis will be performed during the successive recovery phases In addition the ΔtHbPower will be calculated as the ratio between ΔtHb and mean power for each sprint as an index of blood perfusion relative to the intensity of each sprint
Hemoglobin mass measurement
For this measurement 7 blood samples of about 70ul will be taken at the fingertip 5 before CO inhalation and 2 after The CO-rebreathing method consists in the inhalation of a low quantity of CO 1mkg bw mixed with oxygen Having a high affinity for hemoglobin CO binds to the later preferentially To measure total hemoglobin mass the fraction of CO bound to hemoglobin ABL90 Flex Radiometer will be evaluated before and after the inhalation of the mixed gas oxygen CO as well as the CO concentration in the exhaled air CO-meter Dräger
30 s Wingate Test
One hour after the RSA test participants will perform a 10-min warm-up on the cycle ergometer at 30 of their VO2max including two 5-s sprints at a test load Then they will complete a 30-s maximal cycling exercise with a resistance set to 75 of the participants body weight 0075 kgkg bw The participants will be asked to try and generate the highest power possible throughout the test and will receive strong verbal encouragement A 10-min cool down will follow
The investigators will match the male and female participants as closely as possible for sprint performance recorded during the RSA test of Pre- testing The average power of the best two sprints will be calculated in Watts and then expressed as joules per kilogram of lean body mass LBM Moreover the investigators will match participants for VO2max relative to LBM recorded during the incremental test of Pre- testing
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None