Recovery Kinetics After Different Sprint Training Protocols (STRecovery)
STRecovery
1 other identifier
interventional
10
1 country
1
Brief Summary
Speed is one of the most important physical capacities for many sports, especially those that include speed and power as a major element, and plays a major role on performance. Running speed improvement is one of the most basic components of a sprint and power athlete's training program. One of the most commonly used strategies to improve the initial acceleration phase, is resisted sprint training. Sprinting is performed through the stretch-shortening cycle and highly includes the component of eccentric muscle contraction, which can lead to exercise induced muscle damage (EIMD). This phenomenon includes symptoms such as plasma CK elevation, delayed onset of muscle soreness, reduction in force production and a reduction in agility and speed. However, despite the fact that sprint training can cause EIMD symptoms and a performance reduction the following days, research evidence on the recovery kinetics after sprint training are scarce. However, such information is critical for coaches and athletes, in order to effectively design a training program and incorporate the training components in the training microcycle, to avoid injuries and maximize performance. The aim of the present study is to examine the recovery kinetics of EIMD indices, muscle performance and neuromuscular fatigue, after different sprint training protocols.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2021
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 11, 2021
CompletedFirst Posted
Study publicly available on registry
February 23, 2021
CompletedStudy Start
First participant enrolled
March 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 30, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
November 30, 2021
CompletedFebruary 18, 2022
February 1, 2022
9 months
February 11, 2021
February 17, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (29)
Changes in Creatine kinase
CK will be measured in plasma using a Clinical Chemistry Analyzer with commercially available kits.
Baseline (pre), post-, 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in DOMS
DOMS of knee extensors and knee flexors of both lower extremities will be measured during palpation of the muscle belly and the distal regionafter performing three repetitions of a full squat.
Baseline (pre), post-, 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in blood lactate
Lactate will be measured in capillary blood with a hand-portable analyzer.
Baseline (pre), 4 minutes post-trial
Changes in 10m sprint time
20m sprint time will be measured using light cells Chronojump system.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in 20m sprint time
20m sprint time will be measured using light cells Chronojump system.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in 30m sprint time
30m sprint time will be measured using light cells Chronojump system.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in squat jump height
Squat jump height will be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in ground reaction force (GRF) during squat jump
GRF during squat jump will be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak power during squat jump
Peak power during squat jump will be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in mean power during squat jump
Mean power during squat jump will be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in vertical stiffness during squat jump
Vertical stiffness during squat jump will be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak rate of force development (RFD) during squat jump
RFD during squat jump will be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak normalized EMG during squat jump test
Electromyography data will be collected wirelessly at 2000Hz using a Myon MA-320 EMG system (Myon AG, Schwarzenberg, Switzerland) for the vastus lateralis, biceps femoris, gastrocnemius, and tibialis anterior muscles during the concentric phase of the squat jump.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in mean normalized EMG during squat jump test.
Electromyography data will be collected wirelessly at 2000Hz using a Myon MA-320 EMG system (Myon AG, Schwarzenberg, Switzerland) for the vastus lateralis, biceps femoris, gastrocnemius, and tibialis anterior muscles during the concentric phase of the squat jump.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in countermovement jump height
Countermovement jump height will be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in ground reaction force (GRF) during countermovement jump
GRF will be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak power during countermovement jump
Peak power will be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in mean power during countermovement jump
Mean power will be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in vertical stiffness during countermovement jump
Vertical stiffnesswill be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak rate of force development (RFD) during countermovement jump
RFD will be measured on a dynamometer using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of the data for each leg.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak normalized EMG during countermovement jump test
Electromyography data will be collected wirelessly at 2000Hz using a Myon MA-320 EMG system (Myon AG, Schwarzenberg, Switzerland) for the vastus lateralis, biceps femoris, gastrocnemius and gluteus maximum muscles during the eccentric and concentric phases of the countermovement jump test.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in mean normalized EMG during countermovement jump test
Electromyography data will be collected wirelessly at 2000Hz using a Myon MA-320 EMG system (Myon AG, Schwarzenberg, Switzerland) for the vastus lateralis, biceps femoris, gastrocnemius and gluteus maximum muscles during the eccentric and concentric phases of the countermovement jump test.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak concentric torque
Concentric torque of knee extensors and knee flexors will be measured on an isokinetic dynamometer
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak eccentric torque
Concentric torque of knee extensors and knee flexors will be measured on an isokinetic dynamometer
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak isometric torque
Concentric torque of knee extensors and knee flexors will be measured on an isokinetic dynamometer
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in maximal voluntary isometric contraction (MVIC)
MVIC of knee extensors will be measured on an isokinetic dynamometer
Baseline (pre), 1 hour post-, 2 hours post-, 3 hours post-, 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in fatigue rate of maximal voluntary isometric contraction (MVIC)
Fatigue rate during MVIC will be estimated through the percent drop of peak torque between the first and the last three seconds of a 10-second maximal isometric contaction
Baseline (pre), 1 hour post-, 2 hours post-, 3 hours post-, 24 hours post-, 48 hours post-, 72 hours post-trial
Change in field activity during the sprint training protocols
Field activity will be continuously recorded during the sprint training protocols using global positioning system (GPS) technology
Throughout the sprint training protocols
Change in heart rate during the sprint training protocols
Heart rate will be continuously recorded during during the sprint training protocols using heart rate monitors
Throughout the sprint training protocols
Secondary Outcomes (7)
Body weight
Baseline
Body height
Baseline
Body mass index (BMI)
Baseline
Maximal oxygen consumption (VO2max)
Baseline
Body fat
Baseline
- +2 more secondary outcomes
Study Arms (4)
Unresisted sprint training
EXPERIMENTALParticipants will perform an acute training bout of unresisted sprints.
Resisted sprint training with load equal to 10% of body weight
EXPERIMENTALParticipants will perform an acute training bout of resisted sprints with load equal to 10% of body weight.
Resisted sprint training with load equal to 20% of body weight
EXPERIMENTALParticipants will perform an acute training bout of resisted sprints with load equal to 20% of body weight.
Control trial
EXPERIMENTALParticipants will perform no training protocol. They will only perform all the measurements.
Interventions
Particiapants will perform: 2 sets of 3 x 20m sprint 1 set of 3 x 30m sprint
Particiapants will perform: 2 sets of 3 x 20m sprint 1 set of 3 x 30m sprint
Particiapants will perform: 2 sets of 3 x 20m sprint 1 set of 3 x 30m sprint
Eligibility Criteria
You may qualify if:
- Srinters or athletes that comprise sprint training in their training programs
- Absense of musculoskeletal injuries (≥ 6 months)
- Abstence from use of ergogenic supplements or other drugs (≥ 1 month)
- Abstence from participation at exercise with eccentric component (≥ 3 days)
- Abstence from alcohol and energy drings consumption before each experimental trial
You may not qualify if:
- Musculoskeletal injuries (≤ 6 months)
- Use of ergogenic supplements or other drugs (≤ 1 month)
- Participation at exercise with eccentric component (≤ 3 days)
- Alcohol and energy drings consumption before the experimental trials
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Physical Education and Sport Science
Trikala, Thessaly, 42100, Greece
Related Publications (5)
Zafeiridis A, Saraslanidis P, Manou V, Ioakimidis P, Dipla K, Kellis S. The effects of resisted sled-pulling sprint training on acceleration and maximum speed performance. J Sports Med Phys Fitness. 2005 Sep;45(3):284-90.
PMID: 16230978BACKGROUNDBachero-Mena B, Gonzalez-Badillo JJ. Effects of resisted sprint training on acceleration with three different loads accounting for 5, 12.5, and 20% of body mass. J Strength Cond Res. 2014 Oct;28(10):2954-60. doi: 10.1519/JSC.0000000000000492.
PMID: 24736770BACKGROUNDBaird MF, Graham SM, Baker JS, Bickerstaff GF. Creatine-kinase- and exercise-related muscle damage implications for muscle performance and recovery. J Nutr Metab. 2012;2012:960363. doi: 10.1155/2012/960363. Epub 2012 Jan 11.
PMID: 22288008BACKGROUNDDeli CK, Fatouros IG, Paschalis V, Georgakouli K, Zalavras A, Avloniti A, Koutedakis Y, Jamurtas AZ. A Comparison of Exercise-Induced Muscle Damage Following Maximal Eccentric Contractions in Men and Boys. Pediatr Exerc Sci. 2017 Aug;29(3):316-325. doi: 10.1123/pes.2016-0185. Epub 2017 Feb 6.
PMID: 28165870BACKGROUNDPetrakos G, Morin JB, Egan B. Resisted Sled Sprint Training to Improve Sprint Performance: A Systematic Review. Sports Med. 2016 Mar;46(3):381-400. doi: 10.1007/s40279-015-0422-8.
PMID: 26553497BACKGROUND
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Chariklia K Deli, PhD
Department of Physical Education and Sport Science, University of Thessaly
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SCREENING
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
February 11, 2021
First Posted
February 23, 2021
Study Start
March 1, 2021
Primary Completion
November 30, 2021
Study Completion
November 30, 2021
Last Updated
February 18, 2022
Record last verified: 2022-02
Data Sharing
- IPD Sharing
- Will not share