NCT07264751

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
5

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Feb 2014

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2014

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2014

Completed
11.5 years until next milestone

First Submitted

Initial submission to the registry

November 23, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

December 4, 2025

Completed
Last Updated

December 4, 2025

Status Verified

October 1, 2025

Enrollment Period

3 months

First QC Date

November 23, 2025

Last Update Submit

November 23, 2025

Conditions

Keywords

wrestlerscatecholaminesSingle training sessionInflammatory markersHormonal response

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

Sexmale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Location

MeSH Terms

Interventions

Physical Conditioning, Human

Intervention Hierarchy (Ancestors)

ExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Anna Kasperska, PhD

    Poznań University of Physical Education, Faculty of Sport Sciences in Gorzów Wielkopolski, Poland;

    PRINCIPAL INVESTIGATOR

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.

Locations