Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

Autonomic and Peripheral Neurochemical Responses to Maximal Rowing Exercise

15 de setembro de 2026 atualizado por: Poznan University of Physical Education

Integrated Autonomic, Neuroendocrine and Peripheral Neurochemical Responses to Maximal Rowing Exercise and Early Recovery in Elite Athletes

The goal of this observational study is to characterize autonomic, neuroendocrine, and peripheral neurochemical responses to maximal rowing exercise and early recovery in highly trained male athletes.

The main questions it aims to answer are:

  • How do circulating concentrations of cortisol, testosterone, dopamine, serotonin, gamma-aminobutyric acid (GABA), and the testosterone-to-cortisol ratio change in response to maximal rowing exercise and during the first hour of recovery?
  • How do autonomic cardiovascular parameters, including heart rate variability, blood pressure variability, and baroreflex sensitivity, change 3 hours after maximal exercise compared with baseline values?
  • Do endocrine, peripheral neurochemical, and autonomic responses demonstrate similar or divergent recovery patterns following maximal exercise?

Participants will:

  • Perform a maximal 6,000-m rowing ergometer test.
  • Undergo venous blood sampling before exercise, immediately after exercise, and 1 hour after exercise recovery for assessment of endocrine and peripheral neurochemical markers.
  • Undergo noninvasive cardiovascular and autonomic assessment using the Task Force Monitor System before exercise and 3 hours after exercise recovery.

Visão geral do estudo

Status

Concluído

Condições

Descrição detalhada

This observational study was conducted to investigate physiological responses to maximal rowing exercise and subsequent recovery in highly trained male athletes. The study employed a repeated-measures design, allowing assessment of exercise-induced changes across multiple physiological systems during distinct phases of recovery.

Participants completed a maximal 6,000-m rowing ergometer test under standardized laboratory conditions. Biological and physiological measurements were collected before exercise and during recovery according to a predefined protocol. Venous blood samples were obtained at baseline, immediately after exercise, and after 1 hour of recovery. Noninvasive autonomic and cardiovascular assessments were performed using the Task Force Monitor System before exercise and after 3 hours of recovery. The protocol was designed to capture both immediate biochemical responses and delayed autonomic recovery following maximal exercise.

The study focused on endocrine, peripheral neurochemical, and autonomic cardiovascular regulation. Peripheral neurochemical markers were assessed from blood samples and interpreted as components of the peripheral physiological response to exercise rather than direct indicators of central nervous system activity.

Data collection was performed under controlled laboratory conditions using standardized procedures. All measurements were obtained by trained investigators using calibrated equipment. Data quality was verified through routine review of laboratory and physiological recordings. Implausible values and technical artifacts were identified and evaluated before statistical analysis.

The planned sample size was based on the availability of elite athletes meeting the inclusion criteria and the repeated-measures design of the study. Statistical analyses were conducted using repeated-measures approaches appropriate for longitudinal within-subject data. Data distribution was assessed prior to analysis. Parametric or non-parametric tests were applied as appropriate. Effect sizes were calculated to complement significance testing. Associations between selected physiological variables were explored using correlation analyses. Missing data were handled using complete-case analysis, with no imputation procedures applied.

Tipo de estudo

Observacional

Inscrição (Real)

15

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

    • Poznań
      • Poznan, Poznań, Polônia, 61-871
        • Poznań University of Physical Education

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

  • Adulto

Aceita Voluntários Saudáveis

Sim

Método de amostragem

Amostra Não Probabilística

População do estudo

Participants were recruited from the Polish National Rowing Team training at the Olympic Preparation Centre (COS OPO) in Wałcz, Poland.

Descrição

Inclusion Criteria:

  • Highly trained rowers competing at the national or international level
  • Regular participation in structured rowing training
  • Current sports medical clearance for maximal exercise testing
  • Ability to complete a maximal 6,000-m rowing ergometer test
  • Written informed consent to participate in the study

Exclusion Criteria:

  • Acute illness, infection, or injury before testing
  • Diagnosed cardiovascular, metabolic, neurological, endocrine, or inflammatory disorder
  • Use of medications or supplements that could affect cardiovascular, endocrine, metabolic, or neurochemical responses
  • Inability to complete the maximal 6,000-m rowing ergometer test
  • Inability or refusal to provide blood samples
  • Non-compliance with study procedures or pre-test instructions

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

Coortes e Intervenções

Grupo / Coorte
Intervenção / Tratamento
Male elite rowers
Participants completed a single maximal 6,000-m rowing ergometer test. The intervention was distinguished by a standardized all-out rowing protocol combined with peripheral blood sampling before exercise, immediately after exercise, and after 1 hour of recovery, as well as noninvasive autonomic and cardiovascular assessment at baseline and 3 hours after exercise.
Female elite rowers
Participants completed a single maximal 6,000-m rowing ergometer test. The intervention was distinguished by a standardized all-out rowing protocol combined with peripheral blood sampling before exercise, immediately after exercise, and after 1 hour of recovery, as well as noninvasive autonomic and cardiovascular assessment at baseline and 3 hours after exercise.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change from baseline in serum cortisol concentration
Prazo: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Marker of hypothalamic-pituitary-adrenal axis activation and exercise-induced endocrine response.
Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in serum testosterone concentration
Prazo: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Marker of anabolic status and exercise-induced endocrine response.
Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in testosterone-to-cortisol ratio (T/C)
Prazo: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Marker of anabolic-catabolic balance during exercise and recovery.
Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in serum dopamine concentration
Prazo: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Peripheral neurochemical marker associated with physiological responses to exercise and recovery.
Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in serum serotonin concentration
Prazo: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Peripheral neurochemical marker associated with exercise-induced physiological responses and recovery processes.
Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in serum gamma-aminobutyric acid (GABA) concentration
Prazo: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Peripheral neurochemical marker involved in physiological regulatory processes during exercise and recovery.
Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in systolic blood pressure (sBP)
Prazo: Baseline (pre-exercise) and 180 minutes post-exercise.
Continuous beat-to-beat systolic blood pressure measured using the Task Force Monitor System.
Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in diastolic blood pressure (dBP)
Prazo: Baseline (pre-exercise) and 180 minutes post-exercise.
Continuous beat-to-beat diastolic blood pressure measured using the Task Force Monitor System.
Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in mean blood pressure (mBP)
Prazo: Baseline (pre-exercise) and 180 minutes post-exercise.
Continuous beat-to-beat mean arterial pressure measured using the Task Force Monitor System.
Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in heart rate (HR)
Prazo: Baseline (pre-exercise) and 180 minutes post-exercise.
Heart rate derived from continuous electrocardiographic recordings.
Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in total power spectral density of RR intervals (PSD-RRI)
Prazo: Baseline (pre-exercise) and 180 minutes post-exercise.
Total spectral power of heart rate variability obtained from power spectral analysis of RR intervals.
Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in low-frequency power of RR intervals (LF-RRI)
Prazo: Baseline (pre-exercise) and 180 minutes post-exercise.
Low-frequency component of heart rate variability (0.04-0.15 Hz), reflecting combined sympathetic and parasympathetic modulation.
Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in high-frequency power of RR intervals (HF-RRI)
Prazo: Baseline (pre-exercise) and 180 minutes post-exercise.
High-frequency component of heart rate variability (0.17-0.40 Hz), considered an indicator of parasympathetic modulation.
Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in LF/HF ratio
Prazo: Baseline (pre-exercise) and 180 minutes post-exercise.
Ratio of low-frequency to high-frequency spectral power used as an index of sympathovagal balance.
Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in baroreflex sensitivity (BRS)
Prazo: Baseline (pre-exercise) and 180 minutes post-exercise.
Index of baroreflex function calculated using the spontaneous sequence method.
Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in baroreflex effectiveness index (BEI)
Prazo: Baseline (pre-exercise) and 180 minutes post-exercise.
Index quantifying the effectiveness of baroreflex-mediated cardiovascular regulation.
Baseline (pre-exercise) and 180 minutes post-exercise.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Change from baseline in blood lactate concentration
Prazo: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Marker of metabolic response to maximal rowing exercise and early recovery.
Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Cadeira de estudo: Anna Skarpańska-Stejnborn, Professor, Poznan University of Physical Education, Gorzów Wielkopolski; Faculty of Sport Sciences in Gorzów Wielkopolski;

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)

6 de junho de 2024

Conclusão Primária (Real)

25 de novembro de 2024

Conclusão do estudo (Real)

3 de março de 2025

Datas de inscrição no estudo

Enviado pela primeira vez

16 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

16 de junho de 2026

Primeira postagem (Real)

22 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

18 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

15 de setembro de 2026

Última verificação

1 de junho de 2024

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Descrição do plano IPD

Individual participant data sharing has not yet been determined. Future sharing of de-identified data will depend on institutional policies, ethical considerations, participant consent, and planned secondary analyses.

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 .

Se inscrever