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Recovery Kinetics Following Eccentric Exercise

7 de junho de 2022 atualizado por: Ioannis G. Fatouros, University of Thessaly

Recovery Kinetics Following Three Exercise-induced Muscle Damage Protocols in Adult Males

The aim of this study will be to investigate the recovery kinetics of neuromuscular fatigue, muscle microtrauma indicators, performance and oxidative stress factors after three different exercise induced muscle damage (EIMD) protocols in adult Males. Also, this study will determine the comparison among three different eccentric protocols in neuromuscular fatigue, muscle microtrauma indicators, performance and oxidative stress factors. The eccentric protocols will be differentiated in training volume and specifically in the eccentric repetitions in isokinetic dynamometer.

Visão geral do estudo

Descrição detalhada

It is known that eccentric exercise induces muscle microtrauma. Also, eccentric type of exercise are associated with inflammatory response. The leukocytes and the immune cells during the phagocytosis process alter the redox status causing secondary muscle damage to the muscle tissue and also increase oxidative stress concentration. Despite of the existence of studies that examine the muscle damage indicators, inflammatory response, performance and neuromuscular fatigue and oxidative stress concentrations after eccentric exercise, however no studies are detected in order to compare the differences among three eccentric protocols. The eccentric protocols will be differentiated in training volume and specifically in the eccentric repetitions in isokinetic dynamometer. Specifically, a randomized, fourth-trial, cross-over, repeated measures design will be applied. Healthy male adults (age 18-30 years) will participate in the present study. Also, it is considered necessary that the participants will not suffer from any musculoskeletal injuries that will limit their ability to perform the exercise protocols. Also the participants will not be smokers and will not consume alcohol and nutritional supplements.

In the first phase all participants will sign an informed consent form after they will be informed about all benefits and risks of this study and they will sign a recent historical of musculoskeletal injury or illness form. Subsequently, fasting blood samples will be collected by venipuncture using a disposable needle (20-gauge) in order to measure muscle damage markers (CK), inflammation markers (WBC) and oxidative stress markers (TBARS, PC, GSH, ΤΑC, CAT, UA). After, delayed onset muscle soreness (DOMS) in the knee flexors (KF) and extensors (KE) of both limbs, body weight (BW), height and body composition (DXA method) will be measured in the lab. Completing the first phase, participants will be instructed by a dietitian how to record a 5 days diet recalls estimating the energy intake during the trials will be the same. The knee range of motion (KJRM) will be determined by the use of a goniometer, 24 hours after (second phase). The counter movement jump (CMJ) will be evaluated on a force platform 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. During the CMJ will be measured the jump height (cm), the ground reaction force (N), the peak and mean power (W/kg), the vertical stiffness (Kvert, N/m/kg) and the peak rate of force development (RFD, N/s), while at the same time will be evaluated the change in peak and mean normalized EMG during the eccentric and concentric phases of the counter movement jump, for the vastus medialis (VM) and vastus lateralis muscles. Electromyography data will be collected wirelessly at 2.000 Hz using a Myon MA-320 EMG system. The peak eccentric and concentric isokinetic torque of the knee flexors and extensors, in both limbs will be evaluated on an isokinetic dynamometer at 60°/sec. Also, the isometric peak torque of the knee extensors will be evaluated at 65° in both limbs. Finally, Open-circuit spirometry will be utilized for assessment of maximal oxygen consumption (VO2max) using an automated online pulmonary gas exchange system via breath-by-breath analysis during a graded exercise testing on a treadmill.

96 hours after, the participants are going to perform one of the three eccentric protocols randomly, on an isokinetic dynamometer. The eccentric protocol will be performed on a different limb for each trial. The ECC 75 trial will include 75 eccentric maximum repetitions (5 sets, 15 reps/set and recovery period: 30sec.) at 60°/sec. The ECC 150 trial will include 150 eccentric maximum repetitions (10 sets, 15 reps/set and recovery period: 30sec.) at 60°/sec. The ECC 300 trial will include 300 eccentric maximum repetitions (20 sets, 15 reps/set and recovery period: 30sec.) at 60°/sec. The DOMS indicator in the knee flexors (KF) and extensors (KE) of both limbs and the KJRM will be evaluated immediately after each protocol. Also, the (CMJ) will be evaluated on a force platform 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. During the CMJ will be measured the jump height (cm), the ground reaction force (N), the peak and mean power (W/kg), the vertical stiffness (Kvert, N/m/kg) and the peak rate of force development (RFD, N/s), while at the same time will be evaluated the change in peak and mean normalized EMG during the eccentric and concentric phases of the counter movement jump, for the vastus medialis (VM) and vastus lateralis muscles. Electromyography data will be collected wirelessly at 2.000 Hz using a Myon MA-320 EMG system. In addition, the peak eccentric and concentric isokinetic torque of the knee flexors and extensors, in both limbs will be evaluated on an isokinetic dynamometer at 60o/sec. Also, the isometric peak torque of the knee extensors will be evaluated at 65o in both limbs. All the above markers will be evaluated 24, 48 and 192 hours post eccentric protocol, however at these time points, fasting blood samples (20ml) will be collected in order to estimate hematological and biochemical indicators. Α 2 - week washout period will be adapted among trials. After, the participants will perform the process until they complete the trials.

Tipo de estudo

Intervencional

Inscrição (Real)

10

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

      • Tríkala, Grécia, 42100
        • University o Thessaly, School of Physical Education and Sports Science

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos a 30 anos (Adulto)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Macho

Descrição

Inclusion Criteria:

  • Aged between 18 and 30 years
  • Body Mass Index between 18.5-24.9 kg/m*m
  • Free of chronic diseases
  • Free of musculoskeletal injury
  • participants should be non-smokers

Exclusion Criteria:

  • Musculoskeletal injury
  • Chronic disease
  • Use of alcohol, caffeine and any type of nutritional supplements or medication before (≥ 6 months) and throughout the study.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Ciência básica
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição cruzada
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Sem intervenção: Ao controle
Os participantes neste braço não receberão nenhuma intervenção.
Experimental: Eccentric 75
Participants in this arm will perform an eccentric exercise protocol consisted of 75 eccentric repetetions on an isokinetic dynamometer.
An acute bout of eccentric exercise will be performed on an isokinetic dynamometer, including 5 sets of 15 repetitions, with 30 sec rest intervals,at 60 degrees/sec.
Experimental: Eccentric 150
Participants in this arm will perform an eccentric exercise protocol consisted of 150 eccentric repetetions on an isokinetic dynamometer.
An acute bout of eccentric exercise will be performed on an isokinetic dynamometer, including 10 sets of 15 repetitions, with 30 sec rest intervals,at 60 degrees/sec.
Experimental: Eccentric 300
Participants in this arm will perform an eccentric exercise protocol consisted of 300 eccentric repetetions on an isokinetic dynamometer.
An acute bout of eccentric exercise will be performed on an isokinetic dynamometer, including 20 sets of 15 repetitions, with 30 sec rest intervals,at 60 degrees/sec.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in white blood cell count
Prazo: At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
White blood cell count will be measured using an automatic blood analyzer
At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in catalase activity
Prazo: At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Concentration of catalase will be measured in red blood cells
At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in uric acid in plasma
Prazo: At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
concentration of uric acid will be measured in plasma
At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in protein carbonyls in blood
Prazo: At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Concentration of protein carbonyls will be measured in red blood cells
At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in total antioxidant capacity
Prazo: At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
total antioxidant capacity will be measured in serum
At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in reduced glutathione in blood
Prazo: At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Concentration of oxidized glutathione will be measured in red blood cells
At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in thiobarbituric acid reactive substances
Prazo: At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Thiobarbituric acid will be measured in plasma
At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in Creatine kinase in blood
Prazo: At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Creatine kinase will be measured in plasma
At baseline, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in countermovement jump height
Prazo: At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Countermovement jump height will be measured 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 data for each leg.
At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Change in ground reaction force (GRF) during countermovement jump test
Prazo: At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
The ground reaction force will be measured 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 GRF data for each leg.
At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Change in peak power during countermovement jump test
Prazo: At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
The peak power will be measured 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 peak power data for each leg.
At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Change in mean power during countermovement jump test
Prazo: At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
The mean power will be measured 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 mean power data for each leg.
At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Change in vertical stifness during countermovement jump test
Prazo: At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
The vertical stiffness will be measured using two force platforms at 1000 Hz, with each foot in parallel on the two platforms providing a separate yet time-synchronized measurement of vertical stifness data for each leg.
At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Change in peak rate of force develpemnt during countermovement jump test
Prazo: At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
The Peak rate of force development will be measured 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 Peak RFD data for each leg.
At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Change in peak normalized EMG during the eccentric and concentric phases of the counter movement jump
Prazo: At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Electromyography data will be collected wirelessly at 2.000 Hz using a Myon MA-320 EMG system (Myon AG, Schwarzenberg, Switzerland) for the vastus medialis (VM) and vastus lateralis muscles.
At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Change in mean normalized EMG during the eccentric and concentric phases of the counter movement jump
Prazo: At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Electromyography data will be collected wirelessly at 2.000 Hz using a Myon MA-320 EMG system (Myon AG, Schwarzenberg, Switzerland) for the vastus medialis (VM) and vastus lateralis muscles.
At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Change in knee range of motion
Prazo: At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Knee range of motion will be measured by goniometer
At baseline, at 1 hour and 24, 48 and 192 hours following the eccentric exercise protocol.
Change in eccentric isokinetic knee extensors peak torque
Prazo: At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
Eccentric isokinetic knee extensors peak torque will be assessed on an isokinetic dynamometer
At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in concentric isokinetic knee extensors peak torque
Prazo: At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
Concentric isokinetic knee extensors peak torque will be assessed on an isokinetic dynamometer
At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in eccentric isokinetic knee flexors peak torque
Prazo: At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
Eccentric isokinetic knee flexors peak torque will be assessed on an isokinetic dynamometer
At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in concentric isokinetic knee flexors peak torque
Prazo: At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
Concentric Iisokinetic knee flexors peak torque will be assessed on an isokinetic dynamometer
At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in isometric peak torque
Prazo: At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
The isometric peak torque will be assessed on an isokinetic dyanmometer
At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in fatigue index of isometric torque during 10 second
Prazo: At baseline, 1hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
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-secong maximal isometric contraction.
At baseline, 1hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
Change in delayed onset of muscle soreness (DOMS) in the knee flexors (KF) and extensors (KE) of both limbs
Prazo: At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.
Muscle soreness (KF and KE) will be assessed during palpation of the muscle belly and the distal region
At baseline, 1 hour, at 24, 48 and 192 hours following the eccentric exercise protocol.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Peso corporal
Prazo: Na linha de base
O peso corporal será medido em uma balança de trave com estadiômetro
Na linha de base
Altura
Prazo: Na linha de base
A altura corporal será medida em uma balança de trave com estadiômetro
Na linha de base
Corpo gordo
Prazo: Na linha de base
A gordura corporal será medida usando absorciometria de raios X de dupla emissão
Na linha de base
Dietary intake
Prazo: Over a 5 -day period at baseline
Dietary intake will be assessed using 5 -day diet recalls
Over a 5 -day period at baseline
Consumo máximo de oxigênio (VO2max)
Prazo: Na linha de base
O consumo máximo de oxigênio será medido por espirometria de circuito aberto através do método respiração por respiração
Na linha de base

Colaboradores e Investigadores

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Patrocinador

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

1 de abril de 2021

Conclusão Primária (Real)

28 de fevereiro de 2022

Conclusão do estudo (Real)

30 de abril de 2022

Datas de inscrição no estudo

Enviado pela primeira vez

25 de janeiro de 2021

Enviado pela primeira vez que atendeu aos critérios de CQ

30 de janeiro de 2021

Primeira postagem (Real)

2 de fevereiro de 2021

Atualizações de registro de estudo

Última Atualização Postada (Real)

10 de junho de 2022

Última atualização enviada que atendeu aos critérios de controle de qualidade

7 de junho de 2022

Última verificação

1 de junho de 2022

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • Recovery-Eccentrics-UTH

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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