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Impact of Respiratory Training on Reaction Time and Other Performance Components in Young Football Players.

27 luglio 2026 aggiornato da: Laura Piejko, The Jerzy Kukuczka Academy of Physical Education in Katowice

The Impact of Respiratory Training on Reaction Time and Other Components of Performance in Young Football Players.

The overall aim of the study is to gain knowledge about the impact of respiratory training on reaction time and other components of performance in young football players.

Panoramica dello studio

Stato

Non ancora reclutamento

Intervento / Trattamento

Descrizione dettagliata

The specific aims of the study are to answer whether physical training extended with respiratory exercises increases reaction time, agility, speed and endurance in young football players. An application goal of the study is to gain knowledge whether physical training supplemented with breathing exercises improve reaction time, agility, speed, and exercise capacity in young football players.

The study will include 50 healthy football players aged 13 to 15 (born in 2011-2013), who have been playing football for at least two years and are members of the MTS Rybnik Football Academy.

After obtaining written consent to participate in the study and meeting the inclusion criteria all participants will be assigned to the experimental group and the control group (25 people in each group).

Randomization will be conducted using sequentially numbered, opaque, sealed envelopes (SNOSE).

Tipo di studio

Interventistico

Iscrizione (Stimato)

50

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Silesian Voivodeship
      • Katowice, Silesian Voivodeship, Polonia, 40-065
        • Jerzy Kukuczka Academy of Physical Education in Katowice
        • Contatto:
        • Investigatore principale:
          • Anna Polak, Prof.
      • Rybnik, Silesian Voivodeship, Polonia, 44-200
        • MTS Rybnik Football Academy in Rybnik

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino

Accetta volontari sani

Sì

Descrizione

Inclusion Criteria 50 healthy boys aged 13-15 (born between 2011 and 2013) who:

  • are training in football for at least 2 years;
  • have a valid medical clearance to practice football,
  • nave an active membership in the MTS Rybnik Football Academy,
  • have parental/caregiver consent for the participation in the study,
  • give an informed consent to participate in the study,
  • did not participate in respiratory or other breathing training over the past year,
  • are attending the training sessions during the 6 months prior to the study at a level of at least 80% of scheduled hours.

Exclusion Criteria:

  • no valid medical clearance to practice football,
  • currently occurring acute (including respiratory infections) or chronic diseases that may affect sport endurance and safety of training,
  • musculoskeletal injuries requiring treatment or limiting participation in football training, sustained within the 6 months prior to participation in the study,
  • illnesses requiring hospitalization within the 6 months prior to participation in the study,
  • neurological or musculoskeletal conditions requiring physiotherapy within the 6 months prior to participation in the study,
  • diagnosed respiratory diseases (e.g., pharmacologically uncontrolled asthma), cardiovascular diseases, or other conditions constituting a contraindication to sports and physical exertion,
  • contraindications to performing breathing and respiratory exercises, such as: a tendency toward hyperventilation, dizziness during breathing exercises, or recent chest injuries.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Nessun intervento: Control group N=25

A standard football football training will be carried out at the MTS Football Academy in Rybnik, Poland in accordance with the applicable training program for the given age category. The training will include technical, tactical, and general development exercises, including elements of speed, agility, coordination and endurance training, carried out in the form of individual and team exercises and task games. The intensity and volume of training will be adapted to age, level of advancement and current stage of the season training.

+ 4-week follow-up

Sperimentale: Experimental group N= 25 with respiratory training

A standard football training will be carried out at the MTS Football Academy in Rybnik, Poland.

In the experimental group, respiratory training will also be implemented. This training will be supplementary, low-intensity and will provide relaxation. It will not interfere with the main and total training load of the athletes.

Exercises will be conducted for 4 weeks, 3 times per week, immediately after the football training unit. Each breathing training session will last about 20 minutes and will be performed in a supine position, in conditions conducive to relaxation and concentration on breathing. Respiratory training will be introduced progressively, taking into account the gradual adaptation of athletes to the exercises.

Week 1 Relaxation exercises using gentle diaphragmatic breathing, learning the correct diaphragmatic breathing, elements of prolonged exhalation exercises, final relaxation.

Week 2 The session will be extended with diaphragmatic breathing with a gradual increase in resistance, achieved by controlled increase of resistance of the abdominal tissues and short rest phases between exercises.

Week 3 and 4 The respiratory training will be supplemented with: diaphragmatic breathing with resistance manually dosed by the supervising physiotherapist, through a gentle, controlled pressure on the abdomen during the inhalation phase, exercises aimed at activating the lower ribs muscles activity, short elements of chest breathing as a supplementary exercise, final relaxation.

The protocol is based on methods used in respiratory training in clinical studies involving athletes, including young soccer players with a proven beneficial effect on exercise capacity and fatigue tolerance.

+4-week follow-up

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Reaction time test using BlazePod sensors
Lasso di tempo: From enrollment to the end of treatment and after 2 and 4 weeks

Reaction time test using BlazePod sensors - assessment of selective reaction time.

Rapid visuomotor reaction is an important element of football, in which the player makes decisions in dynamically changing field conditions [Nakamoto, Mori 2008]. To assess the reaction time, the BlazePod light-sensor system will be used, which enables an objective measurement of reaction speed to randomly appearing visual stimuli and is widely used in sports training.

Sensors will be placed on the ground, and the subject's task will be to touch the randomly illuminated sensor as quickly as possible. Each player will perform five assessments, and for statistical analysis the mean of the three best results will be used.

From enrollment to the end of treatment and after 2 and 4 weeks
T-Drill Test
Lasso di tempo: From enrollment to the end of treatment and after 2 and 4 weeks
T-Drill Test - assessment of agility and speed of change of direction of movement The T-Drill Test is a commonly used tool for assessing agility, acceleration, and the ability to quickly change the direction of movement in team sports, including soccer [Pauole et al. 2000]. Four cones will be set up in the shape of the letter "T". The player starts from a standing position at the central point, runs forward for a distance of 10 meters, then performs lateral movements to the left and to the right, returns to the center, and runs backward to the starting location. Time measurement will be carried out using an electronic stopwatch or photogates. Each player will perform two trial runs and then two proper trials; for statistical analysis the best obtained result will be used.
From enrollment to the end of treatment and after 2 and 4 weeks
Sprint over 30 meters
Lasso di tempo: From enrollment to the end of treatment and after 2 and 4 weeks
Sprint over 30 meters - assessment of running speed Running over a distance of 30 meters is a standard method for assessing speed and acceleration ability, constituting an important predictor of the effectiveness of offensive and defensive football playing [Haugen et al. 2012]. Time measurement will be conducted over a 30-meter section. The player will start the run from a standing position. Running time will be measured using photogates or an electronic stopwatch. The test will be performed twice, and for statistical analysis the best of the obtained times will be considered.
From enrollment to the end of treatment and after 2 and 4 weeks
Yo-Yo IR1 Test
Lasso di tempo: From enrollment to the end of treatment and after 2 and 4 weeks

Yo-Yo Intermittent Recovery Test (Yo-Yo IR1) - assessment of exercise capacity The Yo-Yo IR1 Test is a widely used and well described in the literature tool for assessing aerobic and anaerobic capacity in intermittent sports, such as football [Bangsbo et al. 2008]. The test allows assessing the ability to perform repeated high-intensity efforts and the effectiveness of recovery between them. The player performs shuttle runs between lines spaced 20 meters apart, accordingto the pace set by an audio signal. After each double shuttle run (2 x 20 m), a short active break is performed, including a jog over a distance of 5 meters and a return to the start line. The test is ended at the moment when the athlete is unable to reach the line twice within the allotted time.

Test will be conducted one time.

From enrollment to the end of treatment and after 2 and 4 weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Anna Polak, Prof., The Jerzy Kukuczka Academy of Physical Education, Katowice, Poland

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 settembre 2026

Completamento primario (Stimato)

30 aprile 2027

Completamento dello studio (Stimato)

30 giugno 2027

Date di iscrizione allo studio

Primo inviato

27 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

27 luglio 2026

Primo Inserito (Effettivo)

30 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

30 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

27 luglio 2026

Ultimo verificato

1 marzo 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Descrizione del piano IPD

Undecided

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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