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Autonomic and Peripheral Neurochemical Responses to Maximal Rowing Exercise

15 settembre 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Completato

Condizioni

Descrizione dettagliata

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 di studio

Osservativo

Iscrizione (Effettivo)

15

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

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

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

Sì

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

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

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change from baseline in serum cortisol concentration
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change from baseline in blood lactate concentration
Lasso di tempo: 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.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Cattedra di studio: Anna Skarpańska-Stejnborn, Professor, Poznan University of Physical Education, Gorzów Wielkopolski; Faculty of Sport Sciences in Gorzów Wielkopolski;

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

6 giugno 2024

Completamento primario (Effettivo)

25 novembre 2024

Completamento dello studio (Effettivo)

3 marzo 2025

Date di iscrizione allo studio

Primo inviato

16 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

16 giugno 2026

Primo Inserito (Effettivo)

22 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

18 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

15 settembre 2026

Ultimo verificato

1 giugno 2024

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Descrizione del piano 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.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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