Recovery Kinetics Following Change of Direction Training

Sponsor
University of Thessaly (Other)
Overall Status
Recruiting
CT.gov ID
NCT04795232
Collaborator
(none)
10
2
3
18
5
0.3

Study Details

Study Description

Brief Summary

This study aims at investigating the recovery kinetics of skeletal muscle damage, neuromuscular fatigue and performance following a single change of direction (COD) training session in competitive soccer players. The impact of COD degrees will be also examined by comparing a 45o vs. 90o COD training session. Ten male soccer players will perform a COD45 [A single training session including 2x(10x ~27.6m) sprints with two 45o COD in each sprint], a COD90 [A single training session including 2x(10x ~21.2m) sprints with two 90o COD in each sprint] and a Control trial (No intervention included, only daily measurements) in randomized, repeated measures, crossover design. Assessments related to skeletal muscle damage, neuromuscular fatigue and performance will be performed prior to training session and daily for three consecutive days post-training, in each trial.

Condition or Disease Intervention/Treatment Phase
  • Other: COD45
  • Other: COD90
N/A

Detailed Description

Ten male soccer players will be included in this study. Participants will be initially informed about the aim of study as well as the associated risks and benefits and subsequently will provide their signed consent form. At baseline, they will undergo assessment of their anthropometrics (i.e. body mass and body height), body composition (by DXA), physical conditioning status [maximal oxygen consumption (VO2max), Yo-Yo Intermittent Endurance test level 2 and Yo-Yo Intermittent Recovery test level 2] and daily dietary intake. Thereafter, they will participate in two experimental trials and one control trial in a randomized, crossover, repeated measures design: i) COD45: Participants in this trial will perform a COD training session consisted of 2 sets of 10 x ~27.6m sprints with two 45o COD in each sprint and a resting period of 16 sec and 2:20 min between sprints and sets, respectively, ii) COD90: Participants in this trial will perform a COD training session consisted of 2 sets of 10 x ~21.2m sprints with two 90o COD in each sprint and a resting period of 16 sec and 2:20 min between sprints and sets, respectively, iii) Control: Participants in this trial will only participate in daily assessments to control for day to day variability in the depended variables (they will not receive any intervention). Prior to each trial, participants will provide a resting blood sample (for the determination of blood lactate, white blood cell count and creatine kinase activity) and undergo assessment of their delayed onset of muscle soreness (DOMS), maximal voluntary isometric contraction (MVIC), countermovement jump [will be assessed using two force platforms at 1000 Hz and electromyography instrumentation (EMG)], isokinetic peak torque of knee extensors and flexors (will be assessed on an isokinetic dynamometer), agility (will be assessed using the Illinois test), 10m and 30m sprint time (will be assessed by using light cells) and repeated sprint ability (5x30m sprints will be performed with 25 sec rest in-between). In COD45 and COD90 experimental trials, a blood sample will be collected immediately post-training for the determination of blood lactate concentration while assessment of DOMS, MVIC and countermovement jump will be performed at 1, 2 and 3 hours post-training. In all trials assessment of DOMS, MVIC, countermovement jump (CMJ), isokinetic peak torque, agility and sprinting performance as well as determination of creatine kinase activity and white blood cell count will be performed at 24, 48 and 72 hours post-training. A 7-day wash out period will applied between trials.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Recovery Kinetics Following Change of Direction (COD) Training in Soccer: Implications for Different COD Angles
Actual Study Start Date :
Apr 1, 2021
Actual Primary Completion Date :
Sep 30, 2021
Anticipated Study Completion Date :
Sep 30, 2022

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control

Participants in this arm will receive no intervention

Experimental: COD45

Participants in this arm will participate in a COD training session consisted of 45 degrees changes of direction

Other: COD45
Participants will perform 2 sets of 10 sprints. The total distance for each sprint will be 27.6 meters and will include two changes of direction of 45 degrees. The recovery time will be 16 seconds between sprints and 2.20 minutes between sets

Experimental: COD90

Participants in this arm will participate in a COD training session consisted of 90 degrees changes of direction

Other: COD90
Participants will perform 2 sets of 10 sprints. The total distance for each sprint will be 21.2 meters and will include two changes of direction of 90 degrees. The recovery time will be 16 seconds between sprints and 2.20 minutes between sets

Outcome Measures

Primary Outcome Measures

  1. Change in creatine kinase activity [At baseline, at 24, 48 and 72 hours after change of direction training session]

    Creatine kinase activity will be measured in plasma

  2. Change in white blood cell count [At baseline, at 24, 48 and 72 hours after change of direction training session]

    White blood cell count will be measured by using an automatic blood analyzer

  3. Change in delayed onset of muscle soreness [At baseline, at 1, 2, 3, 24, 48 and 72 hours after change of direction training session]

    Muscle soreness will be assessed by palpation of the muscle belly and the distal region

  4. Change in isometric peak torque [At baseline, at 1, 2, 3, 24, 48 and 72 hours after change of direction training session]

    Isometric peak torque will be assessed on an isokinetic dynamometer

  5. Change in fatigue index of maximal voluntary isometric contraction during 10 seconds [At baseline, at 1, 2, 3, 24, 48 and 72 hours after change of direction training session]

    Fatigue rate will be determined by calculating the percent drop of peak torque between the first and the last three seconds of a 10-second maximal isometric contraction

  6. Change in isokinetic peak torque of knee extensors [At baseline, at 24, 48 and 72 hours after change of direction training session]

    Isokinetic peak torque will be assessed on an isokinetic dynamometer in both limbs

  7. Change in isokinetic peak torque of knee flexors [At baseline, at 24, 48 and 72 hours after change of direction training session]

    Isokinetic peak torque will be assessed on an isokinetic dynamometer in both limbs

  8. Change in countermovement jump height [At baseline, at 1, 2, 3, 24, 48 and 72 hours after change of direction training session]

    Countermovement jump height will be assessed by 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 jump height for each leg

  9. Change in ground reaction force during countermovement jump [At baseline, at 1, 2, 3, 24, 48 and 72 hours after change of direction training session]

    Ground reaction force will be assessed by 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 jump height for each leg

  10. Change in peak power during countermovement jump [At baseline, at 1, 2, 3, 24, 48 and 72 hours after change of direction training session]

    Peak power will be assessed 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 jump height for each leg

  11. Change in mean power during countermovement jump [At baseline, at 1, 2, 3, 24, 48 and 72 hours after change of direction training session]

    Mean power will be assessed 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 jump height for each leg

  12. Change in vertical stiffness during countermovement jump [At baseline, at 1, 2, 3, 24, 48 and 72 hours after change of direction training session]

    Vertical stiffness will be assessed 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 jump height for each leg

  13. Change in peak rate of force development during countermovement jump [At baseline, at 1, 2, 3, 24, 48 and 72 hours after change of direction training session]

    Peak rate of force development will be assessed 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 jump height for each leg

  14. Change in peak normalized electromyography (EMG) during the eccentric and concentric phases of the countermovement jump [At baseline, at 1, 2, 3, 24, 48 and 72 hours after change of direction training session]

    EMG data will be collected wirelessly at 2000 Hz using a Myon MA-320 EMG system (Myon AG, Switzerland) for the vastus lateralis, biceps femoris, gastrocnemius and gluteus maximus muscles.

  15. Change in mean normalized electromyography (EMG) during the eccentric and concentric phases of the countermovement jump [At baseline, at 1, 2, 3, 24, 48 and 72 hours after change of direction training session]

    EMG data will be collected wirelessly at 2000 Hz using a Myon MA-320 EMG system (Myon AG, Switzerland) for the vastus lateralis, biceps femoris, gastrocnemius and gluteus maximus muscles.

  16. Change in repeated sprint ability [At baseline, at 24, 48 and 72 hours after change of direction training session]

    Repeated sprint ability will be tested using 5x30 m sprints with 25 seconds rest in-between

  17. Change in sprint time of 10m [At baseline, at 24, 48 and 72 hours after change of direction training session]

    10m sprint time will be assessed using light cells

  18. Change in sprint time of 30m [At baseline, at 24, 48 and 72 hours after change of direction training session]

    30m sprint time will be assessed using light cells

  19. Change in agility [At baseline, at 24, 48 and 72 hours after change of direction training session]

    Agility will be assessed using the illinois agility test.

  20. Change in field activity during the change of direction training session [During the change of direction training session]

    Field activity will be continuously monitored during the change of direction training session by using global positioning system (GPS)

  21. Change in heart rate during the change of direction training session [During the change of direction training session]

    Heart rate will be continuously monitored during the change of direction training session by using heart rate monitors.

  22. Change in blood lactate concentration [At baseline and immediately post change of direction training session]

    Blood lactate will be measured using a lactate plus system

Secondary Outcome Measures

  1. Body mass [At baseline]

    Body mass will me measured on a beam balance with stadiometer

  2. Body height [At baseline]

    Body height will me measured on a beam balance with stadiometer

  3. Body fat [At baseline]

    Body fat will be assessed by using Dual-emission X-ray absorptiometry

  4. Lean body mass [At baseline]

    Lean body mass will be assessed by using Dual-emission X-ray absorptiometry

  5. Maximal oxygen consumption (VO2max) [At baseline]

    VO2max will be measured by open circuit spirometry via breath by breath method

  6. Yo-Yo Intermittent Endurance Test level 2 performance [At baseline]

  7. Yo-Yo Intermittent Recovery Test level 2 performance [At baseline]

  8. Dietary intake [At baseline]

    Dietary intake will be assessed over a 7-day period by using diet recalls

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Soccer players participating in at least 5 training sessions per week and 1official match

  • Participation at a competitive level for at least 4 years

  • Free of musculoskeletal injuries

  • No use of ergogenic supplements or medication

  • Non-smokers

Exclusion Criteria:
  • Musculoskeletal injury

  • Use of alcohol, caffeine and any type of ergogenic supplements or medication during the course of the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 SMART LAB, Department of Physical Education and Sports Science, University of Thessaly. Trikala Greece 42100
2 SmArT LABORATORY, SCHOOL OF PHYSICAL EDUCATION & SPORTS SCIENCES, UNIVERSITY OF THESSALY Trikala Greece 42100

Sponsors and Collaborators

  • University of Thessaly

Investigators

  • Study Director: Ioannis G Fatouros, Prof, University of Thessaly, Department of Physical Education and Sport Science

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ioannis G. Fatouros, Professor, University of Thessaly
ClinicalTrials.gov Identifier:
NCT04795232
Other Study ID Numbers:
  • Recovery-COD Training-UTH
First Posted:
Mar 12, 2021
Last Update Posted:
Jun 28, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ioannis G. Fatouros, Professor, University of Thessaly

Study Results

No Results Posted as of Jun 28, 2022