- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07737379
Impact of Respiratory Training on Reaction Time and Other Performance Components in Young Football Players.
The Impact of Respiratory Training on Reaction Time and Other Components of Performance in Young Football Players.
Visão geral do estudo
Status
Intervenção / Tratamento
Descrição detalhada
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 de estudo
Inscrição (Estimado)
Estágio
- Não aplicável
Contactos e Locais
Contato de estudo
- Nome: Anna Polak, Prof.
- Número de telefone: 32 207 51 00
- E-mail: a.polak@awf.katowice.pl
Estude backup de contato
- Nome: Laura Piejko, PT, PhD
- Número de telefone: 32 207 51 10
- E-mail: l.piejko@awf.katowice.pl
Locais de estudo
-
-
Silesian Voivodeship
-
Katowice, Silesian Voivodeship, Polônia, 40-065
- Jerzy Kukuczka Academy of Physical Education in Katowice
-
Contato:
- Anna Polak, Prof.
- Número de telefone: 32 207 51 00
- E-mail: a.polak@awf.katowice.pl
-
Investigador principal:
- Anna Polak, Prof.
-
Rybnik, Silesian Voivodeship, Polônia, 44-200
- MTS Rybnik Football Academy in Rybnik
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Filho
Aceita Voluntários Saudáveis
Descrição
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.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Dobro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Sem intervenção: 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 |
|
|
Experimental: 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 |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Reaction time test using BlazePod sensors
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
|
Colaboradores e Investigadores
Investigadores
- Investigador principal: Anna Polak, Prof., The Jerzy Kukuczka Academy of Physical Education, Katowice, Poland
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- Resolution no. 01/03/2026
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .