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Completed

NCT Number: NCT07264751

The Effect of a Single Training Session on Changes in Inflammatory, Hormonal, and Metabolic Markers in Athletes.

The study aims to assess the acute response of wrestlers to a single training session. Short-term changes in inflammatory, hormonal, and metabolic markers will be analyzed, which may reflect the development of fatigue and recovery processes following intense exercise. Participation in the study involves performing a standard training session and collecting blood samples at three time points to assess the physiological response. The results will provide a better understanding of the mechanisms of adaptation to exercise in strength and endurance athletes.

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Key information

Sex eligibility

Male

Study type

Observational

Primary location

Poznań University of Physical Education, Faculty of Physical Culture in Gorzów Wielkopolski

Gorzów Wielkopolski, Polska, 66-400, Poland

About this study

The study aims to assess how wrestlers' bodies respond to a single, intense training session. The study focuses on short-term changes in markers of inflammation, the hormonal system (stress hormones, catecholamines), and the metabolic system. This enables a deeper understanding of the physiological mechanisms underlying fatigue development and post-exercise recovery.

Each participant will attend one standard training session, as outlined in the training plan. As part of the study, three venous blood samples will be collected:

  • Before training - at rest, to determine baseline values;
  • Immediately after training;
  • 24 hours after exercise - to evaluate recovery processes.

Blood samples will be analyzed in the lab to determine:

  • inflammatory markers (hsCRP, IL-6, TNF-α),
  • muscle damage marker (CK),
  • stress hormones (adrenaline, noradrenaline, cortisol),
  • metabolic indicators (urea, creatinine, total protein, albumin, uric acid). The project does not require any additional supplementation, dietary changes, or modifications to the training plan.

Participating in the study will provide insights into your individual body's response to intense exercise, including fatigue levels, inflammation, and hormonal balance. The results can help you better tailor your training load and improve your recovery.

Participation in the study is completely voluntary. Participants may withdraw from participation at any time, without giving a reason, without any consequences. Withdrawal from the study will not affect their subsequent athletic training. All data obtained during the study will be treated confidentially and processed solely for scientific purposes. Results will be compiled in aggregate form, preventing the identification of individual participants.

The study protocol was approved by the bioethics committee.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Currently engaged in regular strength-endurance wrestling training.
  • Medically cleared for high-intensity exercise by a sports physician.
  • Willingness to participate and provide written informed consent.
  • Availability to attend the training session and all blood sampling time points (pre-training, immediately post-training, 24 hours post-training)

Exclusion criteria

  • Presence of acute or chronic illness that may affect exercise performance or physiological response
  • Recent musculoskeletal injury limiting participation in high-intensity training.
  • Use of medications or supplements that may interfere with hormonal, inflammatory, or metabolic markers
  • History of endocrine disorders, adrenal insufficiency, or other conditions affecting catecholamine or cortisol levels
  • Inability or unwillingness to comply with study procedures.

Treatment and study plan

physical training

Behavioral

The intervention consists of a standardized, high-intensity wrestling training session designed to simulate typical strength-endurance exercise performed by elite wrestlers. The session includes sport-specific drills, resistance exercises, and aerobic conditioning components appropriate for this athletic discipline. All participants will perform the session under supervision to ensure safety and adherence to the planned intensity and duration.

Primary outcomes

  1. hsCRP

    Time frame: 1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.

    highly sensitive reactive C-protein

  2. CK

    Time frame: 1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.

    creatine kinase

  3. TNF-alpha

    Time frame: 1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.

    tumor necrosis factor alpha

  4. IL-6

    Time frame: 1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.

    Interleukine-6

  5. A

    Time frame: 1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.

    Adrenaline

  6. Noradrenaline

    Time frame: 1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.

    Noradrenaline

Secondary outcomes

  1. Kortisol

    Time frame: 1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.

    Noradrenaline

  2. TP

    Time frame: 1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.

    total protein

  3. Urea

    Time frame: 1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.

    Urea

  4. Albumin

    Time frame: 1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.

    Albumin

Other outcomes

  1. UA

    Time frame: 1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.

    Uric acid

Sponsors and collaborators

Lead sponsor

Poznan University of Physical Education

Other

Registry information

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Dec 4, 2025
Registry last updated
Dec 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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