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Autonomic and Peripheral Neurochemical Responses to Maximal Rowing Exercise

15 września 2026 zaktualizowane przez: 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.

Przegląd badań

Status

Zakończony

Warunki

Szczegółowy opis

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.

Typ studiów

Obserwacyjny

Zapisy (Rzeczywisty)

15

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

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

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły

Akceptuje zdrowych ochotników

Tak

Metoda próbkowania

Próbka bez prawdopodobieństwa

Badana populacja

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

Opis

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

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

Kohorty i interwencje

Grupa / Kohorta
Interwencja / Leczenie
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.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Change from baseline in serum cortisol concentration
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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)
Ramy czasowe: 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.

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Change from baseline in blood lactate concentration
Ramy czasowe: 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.

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Krzesło do nauki: Anna Skarpańska-Stejnborn, Professor, Poznan University of Physical Education, Gorzów Wielkopolski; Faculty of Sport Sciences in Gorzów Wielkopolski;

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

6 czerwca 2024

Zakończenie podstawowe (Rzeczywisty)

25 listopada 2024

Ukończenie studiów (Rzeczywisty)

3 marca 2025

Daty rejestracji na studia

Pierwszy przesłany

16 czerwca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

16 czerwca 2026

Pierwszy wysłany (Rzeczywisty)

22 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

18 września 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

15 września 2026

Ostatnia weryfikacja

1 czerwca 2024

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIEZDECYDOWANY

Opis planu 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.

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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