Respiratory Function and Athletic Performance in Professional Soccer Players

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age18-35
SponsorIstinye University

About this trial

This prospective observational study aims to investigate the relationship between respiratory function and multidimensional athletic performance parameters in professional soccer players. The primary hypothesis of the study is that soccer players with enhanced respiratory function and superior respiratory muscle strength will exhibit optimized motor performance outcomes and shorter (faster) reactive reaction times. Investigators will evaluate respiratory muscle strength, spirometric pulmonary functions, dynamic balance, core and abdominal endurance, and reactive visuomotor reaction times during a single testing session within the competitive season.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Participants will be actively competing, licensed professional soccer players. -Participants will be engaged in regular, team-based training and competitive match schedules.

Participants will voluntarily provide written informed consent before any study-related physical performance assessments are conducted.

Disqualifiers

Participants will be excluded if they present with an acute upper or lower respiratory tract infection that could potentially affect pulmonary function or maximal respiratory muscle performance.

Participants will be excluded if they have a documented history of major cardiothoracic surgery.

Participants will be excluded if they have any diagnosed respiratory and/or cardiovascular disorder associated with dyspnea or impaired pulmonary mechanics.

Participants will be excluded if they present with any condition that elevates clinical risk during maximal inspiratory and expiratory pressure assessments.

Trial population

The study population will consist of elite-level athletic professionals, specifically young adult male professional soccer players. Participants will be recruited from a licensed professional football club actively competing in national league training and competition schedules.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Respiratory and Athletic Performance Assessments

    Other intervention

    Participants will not receive any experimental clinical intervention as part of this observational study. Instead, they will undergo standard, non-invasive physiological and athletic performance screenings during their competitive season. These assessments will include digital respiratory pressure manometry to evaluate maximal inspiratory and expiratory pressures, computerized spirometry to measure pulmonary functions, the Y-Balance Test for dynamic postural stability, the BlazePod wireless LED system for reactive visuomotor reaction times, and sport-specific field tests (isometric plank, 60-second sit-up, and T-drill agility tests) to evaluate core endurance and agility. All measurements will be completed during a single testing session following standardized recovery intervals.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Maximal Expiratory Pressure (MEP)

Description: Respiratory muscle strength will be assessed using a portable digital respiratory pressure meter. Participants will execute a maximal expiratory maneuver from total lung capacity after full inspiration while wearing a nose clip. The highest reproducible value from at least three technically acceptable trials will be recorded in centimeters of water (cmH₂O).

Time frame
2 hours
2

Maximal Inspiratory Pressure (MIP)

Description: Respiratory muscle strength will be assessed using a portable digital respiratory pressure meter. Participants will perform a maximal inspiratory maneuver from residual volume following complete expiration while wearing a nose clip. The highest reproducible value from at least three technically acceptable trials will be recorded in centimeters of water (cmH₂O).

Time frame
2 hour
3

Reactive Visuomotor Reaction Time

Cognitive-motor reaction speed will be quantified using a wireless LED pod system arrayed in an equidistant semi-circular matrix. Participants will utilize their dominant lower limb to deactivate randomly illuminated pods as quickly as possible across 10 sets of 22 randomized stimuli. The mean reaction time across the challenge will be recorded in milliseconds (ms).

Time frame
2 hours
4

Dynamic Postural Stability (Y-Balance Test)

Functional reach capacity and dynamic balance will be quantified using a standardized Y-Balance Test apparatus. While maintaining a single-leg stance, participants will push indicator blocks in the anterior, posteromedial, and posterolateral directions. The maximum reach distance from three successful trials for each direction will be normalized to leg length and used to calculate a comprehensive Composite Score percentage (%) for both limbs.

Time frame
2 hours

Secondary outcomes

1

Forced Vital Capacity (FVC)

Pulmonary function will be evaluated using a computerized spirometry system in accordance with ATS/ERS guidelines. Participants will perform a maximal inspiratory effort followed by a rapid and forceful expiration sustained until complete exhalation. The highest reproducible value will be expressed both as an absolute volume in liters (L) and as a percentage of predicted reference values (FVC%).

Time frame
2 hours
2

Forced Expiratory Volume in 1 Second (FEV1%)

Pulmonary function will be evaluated using a computerized spirometry system in accordance with ATS/ERS guidelines. The volume of air exhaled during the first second of the FVC maneuver will be extracted. The highest reproducible value will be expressed both as an absolute volume in liters (L) and as a percentage of predicted reference values (FEV1%).

Time frame
2 hours
3

Peak Expiratory Flow (PEF)

Pulmonary function will be evaluated using a computerized spirometry system in accordance with ATS/ERS guidelines. The maximum flow rate achieved during the forced expiratory maneuver will be measured. The highest reproducible value will be expressed in liters per second (L/s) and as a percentage of predicted reference values (PEF%).

Time frame
2 hours
4

Dynamic Abdominal Endurance (60-Second Sit-Up Test)

Dynamic muscular endurance of the abdominal wall will be evaluated using a timed sit-up protocol. From a supine position with knees flexed at 90° and hands crossed over the chest, participants will flex the trunk until the elbows touch the knees, then return to the baseline position. The total number of correctly executed repetitions completed within exactly 1 minute (reps) will be recorded.

Time frame
2 hours

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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