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Warm-up of the Inspiratory Musculature and Its Impact in Swimming Performance

12 de maio de 2026 atualizado por: Agustin Velazquez Córdoba, Universidad Rey Juan Carlos

Warm-up of the Inspiratory Musculature and Its Impact on Physiological Parameters and Swimming Performance: Exploration of Intensities Based on Maximal Inspiratory Pressure

Objective To evaluate the acute effect of four inspiratory warm-up intensities (15%, 40%, 60%, and 80% of maximal inspiratory pressure [MIP]) on 100 m freestyle performance, and to analyze their impact on heart rate, blood lactate concentration, perceived exertion, and dyspnea in trained swimmers.

Methods A randomized, crossover, double-blind experimental study was conducted. Participants were swimmers aged ≥18 years, with no respiratory or musculoskeletal pathology.

Each participant completed, in sessions separated by at least three days, an inspiratory muscle warm-up consisting of 30 breaths against resistive loads set at 15%, 40%, 60%, and 80% of their MIP, previously determined using standardized procedures.

Following each intervention, participants performed a maximal 100 m freestyle test. The following variables were recorded:

Swimming time Heart rate (during and post-exercise) Post-exercise capillary blood lactate concentration Rating of perceived exertion (Borg scale) Dyspnea (Dyspnea-12)

Conclusions This study will help identify the optimal inspiratory warm-up intensity to enhance swimming performance.

Visão geral do estudo

Status

Ainda não está recrutando

Condições

Intervenção / Tratamento

Descrição detalhada

Inspiratory warm-up

An intervention performed prior to exercise consisting of breathing against resistance to activate the inspiratory muscles (mainly the diaphragm and accessory respiratory muscles) with the aim of enhancing their performance during subsequent effort.

Maximal Inspiratory Pressure (MIP)

The maximum pressure that an individual can generate during a forceful inspiration against an occluded airway. It is an indicator of inspiratory muscle strength and is used to prescribe training intensity.

Relative intensities (15%, 40%, 60%, 80% of MIP)

Percentages of MIP representing different levels of respiratory workload. They allow graded inspiratory resistance to investigate dose-response effects on performance.

Inspiratory Muscle Training (IMT)

A specific training method targeting the inspiratory muscles through controlled resistive breathing loads, aimed at improving strength, endurance, and ventilatory efficiency.

Crossover design

An experimental design in which each participant completes all experimental conditions, acting as their own control, thereby reducing inter-subject variability.

Double-blind design

A methodological approach in which neither participants nor evaluators are aware of the assigned condition, minimizing bias in performance and outcome assessment.

Swimming performance

A functional outcome measured primarily through time to complete a fixed distance, in this case 100 meters freestyle.

Cardiovascular response

The physiological response of the cardiovascular system to exercise, typically assessed through heart rate and post-exercise recovery dynamics.

Blood lactate concentration

A marker of metabolic stress during high-intensity exercise, reflecting the contribution of anaerobic glycolysis to energy production.

Perceived exertion

A subjective assessment of exercise intensity, commonly measured using standardized scales such as the Borg scale.

Respiratory discomfort (dyspnea)

A subjective sensation of breathing difficulty associated with exertion, reflecting ventilatory demand and exercise tolerance.

Tipo de estudo

Intervencional

Inscrição (Estimado)

52

Estágio

  • Não aplicável

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion criteria:

  • Participants of both sexes, aged over 18 years.
  • Minimum swimming training frequency of at least two sessions per week, with a minimum duration of 30 minutes per session, consistently maintained over the last three months.

Exclusion criteria:

  • Current or previous diagnosis of respiratory diseases.
  • Musculoskeletal injuries limiting the ability to perform a 100-meter swimming test.
  • Participation in inspiratory muscle training programs within the last six months.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição cruzada
  • Mascaramento: Dobro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: IMT: 15%
The study will apply four respiratory warm-up intensities (15%, 40%, 60%, and 80% of maximal inspiratory pressure) to compare their acute effects on these variables. This graded loading approach will allow identification of the optimal dose capable of maximizing diaphragmatic neuromuscular activation without inducing early fatigue, leveraging the post-activation potentiation phenomenon to improve respiratory efficiency and swimming performance.
It is a crossover study in which the different exercise intensities are investigated.
Experimental: IMT:40%
The study will apply four respiratory warm-up intensities (15%, 40%, 60%, and 80% of maximal inspiratory pressure) to compare their acute effects on these variables. This graded loading approach will allow identification of the optimal dose capable of maximizing diaphragmatic neuromuscular activation without inducing early fatigue, leveraging the post-activation potentiation phenomenon to improve respiratory efficiency and swimming performance.
It is a crossover study in which the different exercise intensities are investigated.
Experimental: IMT: 60%
The study will apply four respiratory warm-up intensities (15%, 40%, 60%, and 80% of maximal inspiratory pressure) to compare their acute effects on these variables. This graded loading approach will allow identification of the optimal dose capable of maximizing diaphragmatic neuromuscular activation without inducing early fatigue, leveraging the post-activation potentiation phenomenon to improve respiratory efficiency and swimming performance.
It is a crossover study in which the different exercise intensities are investigated.
Experimental: IMT: 80%
The study will apply four respiratory warm-up intensities (15%, 40%, 60%, and 80% of maximal inspiratory pressure) to compare their acute effects on these variables. This graded loading approach will allow identification of the optimal dose capable of maximizing diaphragmatic neuromuscular activation without inducing early fatigue, leveraging the post-activation potentiation phenomenon to improve respiratory efficiency and swimming performance.
It is a crossover study in which the different exercise intensities are investigated.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
swimming time (100 meters)
Prazo: This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
After the respiratory interventions, participants will perform a maximal 100-meter freestyle swimming test under supervision. The total time will be recorded using a digital stopwatch, starting with the starting signal and ending when the swimmer touches the wall upon completing the distance.
This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Maximal Inspiratory Pressure and Maximal Expiratory Pressure
Prazo: This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Maximal Inspiratory Pressure (PIM/MIP) and Maximal Expiratory Pressure (PEM/MEP) are indicators of global respiratory muscle strength. PIM reflects the maximal negative pressure generated during a forced inspiratory effort against an occluded airway, mainly assessing diaphragmatic and external intercostal muscle function, whereas PEM reflects the maximal positive pressure produced during a forced expiratory effort, mainly involving abdominal and internal intercostal muscles. Both variables are expressed in centimeters of water (cmH₂O) and are widely used to quantify inspiratory and expiratory muscle performance, as well as to evaluate respiratory muscle fatigue and training adaptations in clinical and sports settings.
This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Lactate
Prazo: This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Immediately after the test, blood lactate will be measured using a Lactate Pro 2 portable analyzer, from a capillary blood sample obtained from the fingertip.
This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Perceived exertion.
Prazo: This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Perceived exertion will be assessed using the Borg scale (6-20), previously explained to ensure proper understanding, and will be recorded immediately after exercise through a direct interview.
This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Dysnea
Prazo: This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.

The Dyspnea-12 (D-12) scale is a multidimensional questionnaire used to assess the severity and qualitative perception of dyspnea (breathlessness). It evaluates both the physical and emotional components associated with breathing discomfort.

The questionnaire consists of 12 items:

My breath does not go in all the way My breathing requires more work I feel short of breath I have difficulty catching my breath I cannot get enough air My breathing is uncomfortable My breathing is exhausting My breathing makes me feel depressed My breathing makes me feel miserable My breathing is distressing My breathing makes me agitated My breathing is irritating

Each item is scored using a 4-point Likert scale:

0 = None

  1. = Mild
  2. = Moderate
  3. = Severe

Therefore, the total score ranges from 0 to 36 points.

Interpretation:

A low score indicates little or no perceived dyspnea. A moderate score reflects clinically relevant breathing discomfort. A high score indicates severe dyspnea with an important

This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Heart rate.
Prazo: This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Heart rate will be continuously monitored during the test and for up to five minutes post-exercise using a Polar H10 chest strap, placed on the anterior thoracic region just below the xiphoid process. The device will be calibrated before each session, and data will be analyzed using Polar Flow software to obtain parameters such as mean heart rate, maximum heart rate, which are key indicators of autonomic and cardiovascular response to exercise.
This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Recovery time
Prazo: This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Recovery time will be defined as the period required for heart rate to decrease following the cessation of exercise. This parameter reflects autonomic nervous system recovery, particularly parasympathetic reactivation after physical exertion. Heart rate recovery will be analyzed during the first five minutes post-exercise using data collected from the Polar H10 device. Faster recovery times are generally associated with better cardiovascular fitness and autonomic regulation, whereas delayed recovery may indicate increased physiological stress or fatigue.
This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Heart rate variability
Prazo: This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Heart rate variability (HRV) refers to the variation in the time intervals between consecutive heartbeats (R-R intervals). HRV is considered a non-invasive marker of autonomic nervous system activity and reflects the balance between sympathetic and parasympathetic modulation. HRV data obtained from the Polar H10 sensor will be analyzed using Polar Flow software, and parameters such as RMSSD and SDNN may be extracted. Higher HRV values are typically associated with better autonomic adaptability and recovery capacity, while lower values may reflect fatigue, stress, or reduced physiological adaptability.
This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Forced Vital Capacity and Forced Expiratory Volume in 1 second
Prazo: This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.
Forced Vital Capacity (FVC/CVF) and Forced Expiratory Volume in 1 second (FEV₁) are spirometric measures used to assess ventilatory capacity and pulmonary function. FVC represents the total volume of air that can be forcibly exhaled after a maximal inspiration, expressed in liters (L), while FEV₁ represents the volume exhaled during the first second of that maneuver, also expressed in liters. The FEV₁/FVC ratio is commonly used to identify ventilatory limitations, particularly obstructive patterns. Together, these variables provide key information on airway function, expiratory flow limitation, and overall pulmonary performance.
This measurement will be carried out from the randomization process until 8 weeks after the start of the inspiratory training program.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de setembro de 2026

Conclusão Primária (Estimado)

1 de janeiro de 2027

Conclusão do estudo (Estimado)

1 de janeiro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

19 de abril de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

12 de maio de 2026

Primeira postagem (Real)

19 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

19 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

12 de maio de 2026

Última verificação

1 de fevereiro de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 100220261562026
  • Sponsor-Investigator (Outro identificador: Agustín Velázquez Córdoba)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Descrição do plano IPD

At present, no definitive decision has been made regarding the sharing of individual participant data. On the one hand, making anonymized data available could enhance scientific transparency, reproducibility of results, and the development of new research lines based on the collected data.

However, several relevant aspects are also considered, such as the protection of participant confidentiality, strict compliance with applicable data protection regulations (GDPR), and the need to ensure appropriate and controlled use of the information. Additionally, the potential limitations related to sample size and the specific context of the study are taken into account.

If data sharing is ultimately implemented, it would be provided exclusively in anonymized format, upon justified request, following appropriate project evaluation and, where applicable, through formal data use agreements.

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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 .

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