The Effect of a Single Training Session on Changes in Inflammatory, Hormonal, and Metabolic Markers in Athletes.
1 other identifier
observational
5
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Feb 2014
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2014
CompletedFirst Submitted
Initial submission to the registry
November 23, 2025
CompletedFirst Posted
Study publicly available on registry
December 4, 2025
CompletedDecember 4, 2025
October 1, 2025
3 months
November 23, 2025
November 23, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
hsCRP
highly sensitive reactive C-protein
1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.
CK
creatine kinase
1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.
TNF-alpha
tumor necrosis factor alpha
1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.
IL-6
Interleukine-6
1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.
A
Adrenaline
1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.
Noradrenaline
Noradrenaline
1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.
Secondary Outcomes (4)
Kortisol
1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.
TP
1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.
Urea
1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.
Albumin
1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.
Other Outcomes (1)
UA
1. Before training (at rest), 2. Immediately after training, 3. 24 hours after exercise.
Interventions
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.
Eligibility Criteria
The study participants are elite wrestlers who are also members of a national-level sports club and members of the national team. All athletes have experience competing in international events. The group includes athletes who have won medals at both national and international competitions. Participants are highly trained, with extensive experience in strength-endurance wrestling disciplines, and represent the top competitive level in their sport. The study aims to evaluate acute physiological responses to a single high-intensity training session in this highly specialized discipline.
You may qualify if:
- 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)
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Poznań University of Physical Education, Faculty of Physical Culture in Gorzów Wielkopolski
Gorzów Wielkopolski, Polska, 66-400, Poland
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Anna Kasperska, PhD
Poznań University of Physical Education, Faculty of Sport Sciences in Gorzów Wielkopolski, Poland;
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
November 23, 2025
First Posted
December 4, 2025
Study Start
February 1, 2014
Primary Completion
May 1, 2014
Study Completion
June 1, 2014
Last Updated
December 4, 2025
Record last verified: 2025-10
Data Sharing
- IPD Sharing
- Will not share
IPD will not be shared to protect participant confidentiality and to meet ethical and legal standards regarding sensitive health and performance data.