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
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
| 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 detailed description
| 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:
|
|
Experimental: Structural exercises training
Participants will perform 4 structural (Olympic lifting) exercises
|
Other: Structural exercises training
Participants will perform:
|
|
Experimental: Accentuated eccentric exercises training
Participants will perform 4 exercises with eccentric loading
|
Other: Accentuated eccentric exercises training
Participants will perform:
|
|
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 |
- 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
- 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.
- 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
- 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
- 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
- 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
- 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
- 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
- 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.
- 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.
- 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
- 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
- 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
- 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
- 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
- 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
- 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.
- 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.
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- Body weight [ Time Frame: Baseline ]Body weight will be measured on a beam balance/stadiometer
- Body height [ Time Frame: Baseline ]Body height will be measured on a beam balance/stadiometer
- Body mass index (BMI) [ Time Frame: Baseline ]BMI will be calculated from the ratio of body mass/ body height squared
- Maximal oxygen consumption (VO2max) [ Time Frame: Baseline ]Maximal oxygen consumption will be measured by open circuit spirometry via breath by breath method
- Body fat [ Time Frame: Baseline ]Body fat will be measured by using Dual-emission X-ray absorptiometry
- Lean body mass [ Time Frame: Baseline ]Lean body mass will be measured by using Dual-emission X-ray absorptiometry
- Dietary intake [ Time Frame: Baseline ]Dietary intake will be assessed using 7-day diet recalls
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.
| Ages Eligible for Study: | 18 Years to 30 Years (Adult) |
| Sexes Eligible for Study: | Male |
| Accepts Healthy Volunteers: | Yes |
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
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
| Greece | |
| Chariklia K. Deli | |
| Trikala, Thessaly, Greece, 42100 | |
| Principal Investigator: | Chariklia K Deli, PhD | Department of Physical Education and Sport Science, University of Thessaly |
| 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 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |

