Try the modernized ClinicalTrials.gov beta website. Learn more about the modernization effort.
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Recovery Kinetics After Different Power Training Protocols (PTRecovery) (PTRecovery)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04847427
Recruitment Status : Completed
First Posted : April 19, 2021
Last Update Posted : February 18, 2022
Sponsor:
Information provided by (Responsible Party):
Chariklia K. Deli, University of Thessaly

Brief Summary:
Muscle power is one of the most important parameters in almost every athletic action, expressing the ability of the human muscle to produce great amounts of force with the greatest possible speed. For enhancing their muscle power, athletes comprise several resistance training programs as part of their training. However, muscle power training comprises of eccentric muscle actions, which, especially when unaccustomed, can lead to exercise-induced muscle damage and deterioration of muscle performance. Nevertheless, despite the fact that muscle power training comprises eccentric muscle actions, and consequently can lead to muscle injury and muscle performance reduction during the following days, the recovery kinetics after acute muscle power training have not been adequately studied. However, information regarding the recovery of the muscles after a power training protocol, is critical for the correct design of a training microcycle, and the reduction of injury risk. The aim of the present study is to investigate the muscle injury provoked after acute muscle power training using three different power training exercise protocols. Additionally, the effect of these protocols on muscle performance and neuromuscular fatigue indices will be examined.

Condition or disease Intervention/treatment Phase
Core Exercises Training Structural Exercises Training Accentuated Eccentric Exercises Training Control Condition Other: Core exercises training Other: Structural exercises training Other: Accentuated eccentric exercises training Other: Control trial Not Applicable

Show Show detailed description

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 10 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Screening
Official Title: Recovery Kinetics of Muscle Performance, Muscle Damage and Neuromuscular Fatigue After Different Protocols of Power Training
Actual Study Start Date : April 20, 2021
Actual Primary Completion Date : November 30, 2021
Actual Study Completion Date : November 30, 2021

Arm Intervention/treatment
Experimental: Core exercises training
Participants will perform 4 core exercises
Other: Core exercises training

Participants will perform:

  1. Squats, 4 sets of 5 repetitions at 60% 1RM
  2. Deadlifts, 4 sets of 5 repetitions at 60% 1RM
  3. Lunges, 4 sets of 5 repetitions at 60% 1RM
  4. Step ups, 4 sets of 5 repetitions at 60% 1RM

Experimental: Structural exercises training
Participants will perform 4 structural (Olympic lifting) exercises
Other: Structural exercises training

Participants will perform:

  1. Snatch, 4 sets of 5 repetitions at 60% 1RM
  2. Hang clean, 4 sets of 5 repetitions at 60% 1RM
  3. Push jerk, 4 sets of 5 repetitions at 60% 1RM
  4. Split push jerk, 4 sets of 5 repetitions at 60% 1RM

Experimental: Accentuated eccentric exercises training
Participants will perform 4 exercises with eccentric loading
Other: Accentuated eccentric exercises training

Participants will perform:

  1. Deadlifts - squat jump, 4 sets of 5 repetitions at 30% body mass (BM)
  2. Step down - squat jump, 4 sets of 5 repetitions at 30% BM
  3. Step down - lunges, 4 sets of 5 repetitions at 30% BM
  4. Bulgarian squat jumps, 4 sets of 5 repetitions at 30% BM

Experimental: Control trial
Participants will perform all the measurements that are comprised in the experimental conditions without performing any exercise protocol
Other: Control trial
Participants will perform all the measurements that are comprised in the experimental conditions without performing any exercise protocol




Primary Outcome Measures :
  1. Change in CK in blood [ Time Frame: Baseline (pre), 4 minutes post-, 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Creatine kinase will be measured in plasma using a biochemical analyzer

  2. Change in delayed onset of muscle soreness (DOMS) in the knee flexors (KF) and extensors (KE) of both limbs [ Time Frame: Baseline (pre), 4 minutes post-, 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Participants will perform three repetitions of a full squat movement, and rate their soreness level in knee flexors and extensors on a visual analog scale from 1 to 10 (VAS, with "no pain" at one end and "extremely sore" at the other), using palpation of the belly and the distal region of relaxed knee extensors and flexors.

  3. Change in blood lactate [ Time Frame: Baseline (pre), 4 minutes post-trial ]
    Blood lactate will be measured in capillary blood with a hand-portable analyzer

  4. Change in squat jump height [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Squat jump height will be measured using two force platforms at 1000Hz, with each foot in parallel on the two platforms providing a seperate, yet time-synchronized measurement of the jump height for each leg

  5. Change in ground reaction force (GRF) during squat jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    GRFwill be measured using two force platforms at 1000Hz, with each foot in parallel on the two platforms providing a seperate, yet time-synchronized measurement of the jump height for each leg

  6. Change in peak power during squat jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Peak power will be measured using two force platforms at 1000Hz, with each foot in parallel on the two platforms providing a seperate, yet time-synchronized measurement of the jump height for each leg

  7. Change in mean power during squat jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Mean power will be measured using two force platforms at 1000Hz, with each foot in parallel on the two platforms providing a seperate, yet time-synchronized measurement of the jump height for each leg

  8. Change in vertical stifness during squat jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Vertical stifness will be measured using two force platforms at 1000Hz, with each foot in parallel on the two platforms providing a seperate, yet time-synchronized measurement of the jump height for each leg

  9. Change in peak normalized EMG during the concentric phase of the squat jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    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.

  10. Change in mean normalized EMG during the concentric phase of the squat jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    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.

  11. Change in countermovement jump height [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Countermovement jump height will be measured using two force platforms at 1000Hz, with each foot in parallel on the two platforms providing a seperate yet time-synchronized measurement of the jump height for each leg

  12. Change in ground reaction force (GRF) during countermovement jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Ground reaction force will be measured using two force platforms at 1000Hz, with each foot in parallel on the two platforms providing a seperate yet time-synchronized measurement of the jump height for each leg

  13. Change in peak power during countermovement jump test [ Time Frame: Baseline (pre), post-, 24h post-, 48h post-, 72h post-trial ]
    Peak power will be measured using two force platforms at 1000Hz, with each foot in parallel on the two platforms providing a seperate yet time-synchronized measurement of the jump height for each leg

  14. Change in mean power during countermovement jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Mean power will be measured using two force platforms at 1000Hz, with each foot in parallel on the two platforms providing a seperate yet time-synchronized measurement of the jump height for each leg

  15. Change in vertical stifness during countermovement jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Vertical stifness will be measured using two force platforms at 1000Hz, with each foot in parallel on the two platforms providing a seperate yet time-synchronized measurement of the jump height for each leg

  16. Change in peak rate of force development during countermovement jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Vertical stifness will be measured using two force platforms at 1000Hz, with each foot in parallel on the two platforms providing a seperate yet time-synchronized measurement of the jump height for each leg

  17. Change in peak normalized EMG during the eccentric and concentric phases of the countermovement jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    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.

  18. Change in mean normalized EMG during the eccentric and concentric phases of the countermovement jump test [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    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.

  19. Change in concentric peak torque [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Concentric peak torque will be measured on an isokinetic dynamometer

  20. Change in eccentric peak torque [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Eccentric peak torque will be measured on an isokinetic dynamometer

  21. Change in isometric peak torque [ Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial ]
    Eccentric peak torque will be measured on an isokinetic dynamometer

  22. Change in maximal voluntary isometric contraction (MVIC) during 10 seconds [ Time Frame: Baseline (pre), 1 hour post-, 2 hours post-, 3 hours post-, 24 hours post-, 48 hours post-, 72 hours post-trial ]
    MVIC will be measured on an isokinetic dynamometer

  23. Change in fatigue rate during maximal voluntary isometric contraction (MVIC) [ Time Frame: Baseline (pre), 1 hour post-, 2 hours post-, 3 hours post-, 24 hours post-, 48 hours post-, 72 hours post-trial ]
    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

  24. Differences in field activity between the three different power training protocols [ Time Frame: During each power training protocol ]
    Field activity will be continuously recorded during the power training protocols using global positioning system (GPS) technology

  25. Change in heart rate between the three different power training protocols [ Time Frame: During each power training protocol ]
    Heart rate will be continuously recorded during during the power training protocols using heart rate monitors


Secondary Outcome Measures :
  1. Body weight [ Time Frame: Baseline ]
    Body weight will be measured on a beam balance/stadiometer

  2. Body height [ Time Frame: Baseline ]
    Body height will be measured on a beam balance/stadiometer

  3. Body mass index (BMI) [ Time Frame: Baseline ]
    BMI will be calculated from the ratio of body mass/ body height squared

  4. Maximal oxygen consumption (VO2max) [ Time Frame: Baseline ]
    Maximal oxygen consumption will be measured by open circuit spirometry via breath by breath method

  5. Body fat [ Time Frame: Baseline ]
    Body fat will be measured by using Dual-emission X-ray absorptiometry

  6. Lean body mass [ Time Frame: Baseline ]
    Lean body mass will be measured by using Dual-emission X-ray absorptiometry

  7. Dietary intake [ Time Frame: Baseline ]
    Dietary intake will be assessed using 7-day diet recalls



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 30 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • At least 1 year experience in strength exercises
  • 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

Exclusion Criteria:

  • Less than 1 year experience in strength exercises
  • 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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04847427


Locations
Layout table for location information
Greece
Chariklia K. Deli
Trikala, Thessaly, Greece, 42100
Sponsors and Collaborators
University of Thessaly
Investigators
Layout table for investigator information
Principal Investigator: Chariklia K Deli, PhD Department of Physical Education and Sport Science, University of Thessaly
Publications:

Layout table for additonal information
Responsible Party: Chariklia K. Deli, Assistant Professor, University of Thessaly
ClinicalTrials.gov Identifier: NCT04847427    
Other Study ID Numbers: Power training - Recovery
First Posted: April 19, 2021    Key Record Dates
Last Update Posted: February 18, 2022
Last Verified: February 2022
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No