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Autonomic and Peripheral Neurochemical Responses to Maximal Rowing Exercise

15. September 2026 aktualisiert von: 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.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Detaillierte Beschreibung

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.

Studientyp

Beobachtungs

Einschreibung (Tatsächlich)

15

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

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

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene

Akzeptiert gesunde Freiwillige

Ja

Probenahmeverfahren

Nicht-Wahrscheinlichkeitsprobe

Studienpopulation

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

Beschreibung

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

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

Kohorten und Interventionen

Gruppe / Kohorte
Intervention / Behandlung
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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change from baseline in serum cortisol concentration
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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.

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change from baseline in blood lactate concentration
Zeitfenster: 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.

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

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

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

6. Juni 2024

Primärer Abschluss (Tatsächlich)

25. November 2024

Studienabschluss (Tatsächlich)

3. März 2025

Studienanmeldedaten

Zuerst eingereicht

16. Juni 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

16. Juni 2026

Zuerst gepostet (Tatsächlich)

22. Juni 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

18. September 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

15. September 2026

Zuletzt verifiziert

1. Juni 2024

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

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Beschreibung des IPD-Plans

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.

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Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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