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Physiological Responses to Basketball-Specific Interval Exercise in Female Basketball Players (INTER-BASKET)

11 de agosto de 2026 atualizado por: Poznan University of Physical Education

The Effect of Basketball-Specific Interval Exercise on Metabolic and Inflammatory Responses, Energy Substrate Utilization, and Perceived Fatigue in Female Basketball Players

This study aims to evaluate the effects of interval exercise on metabolic and inflammatory responses, energy substrate utilization, and fatigue in trained female basketball players. High-intensity intermittent exercise is a key component of basketball performance and induces substantial metabolic and physiological stress. However, the acute relationships between exercise-induced metabolic changes, inflammatory responses, substrate utilization, and fatigue in female basketball players remain insufficiently understood.

In this prospective interventional study, eligible female basketball players will complete a standardized interval exercise protocol designed to replicate the physiological demands of competitive basketball. Physiological, biochemical, and perceptual measurements will be collected before exercise, immediately after exercise, and during recovery. Primary outcomes include changes in metabolic and inflammatory biomarkers, energy substrate utilization, and fatigue-related responses. Secondary outcomes include selected physiological and performance-related variables associated with recovery from high-intensity interval exercise.

The findings of this study will improve the understanding of the physiological responses to interval exercise in female basketball players and may contribute to the development of evidence-based training and recovery strategies aimed at optimizing performance and athlete health.

Visão geral do estudo

Status

Ainda não está recrutando

Descrição detalhada

High-intensity intermittent exercise is a fundamental component of basketball and is characterized by repeated bouts of sprinting, jumping, rapid changes of direction, and brief recovery periods. This type of exercise places substantial demands on both aerobic and anaerobic energy systems and induces complex metabolic and inflammatory responses. Although numerous studies have investigated the physiological effects of high-intensity exercise, the interactions among exercise-induced inflammation, metabolic regulation, energy substrate utilization, and fatigue in female basketball players remain insufficiently understood.

The purpose of this study is to investigate the acute effects of basketball-specific interval exercise on metabolic and inflammatory responses, energy substrate utilization, and psychophysiological fatigue in trained female basketball players. The exercise stimulus will consist of the Yo-Yo Intermittent Recovery Test Level 1 (Yo-Yo IR1), a validated field test that closely simulates the intermittent high-intensity demands of competitive basketball by requiring shuttle runs interspersed with short active recovery periods.

Participants will attend a single experimental session consisting of baseline assessments, completion of a standardized interval exercise protocol, and follow-up assessments during the early recovery period. Biological samples, physiological measurements, and fatigue assessments will be obtained at predefined time points before exercise, immediately after exercise, and one hour after exercise. Laboratory analyses will evaluate selected inflammatory and metabolic biomarkers together with indicators of energy substrate utilization. In addition, subjective fatigue and neuromotor performance will be assessed to characterize both peripheral and central aspects of exercise-induced fatigue.

To minimize potential confounding factors, participants will follow standardized pre-test instructions regarding physical activity, alcohol consumption, caffeine intake, and nutritional preparation before testing. Nutritional intake and anthropometric characteristics will also be documented to support the interpretation of physiological responses.

By integrating biochemical, metabolic, physiological, and psychophysiological measurements within a basketball-specific exercise model, this study aims to improve understanding of the mechanisms underlying acute responses to high-intensity intermittent exercise in female athletes. The findings may contribute to evidence-based strategies for monitoring training load, optimizing recovery, and improving performance in women's basketball and other intermittent team sports.

Tipo de estudo

Intervencional

Inscrição (Estimado)

25

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

      • Gorzów Wielkopolski, Polônia, 66-400
        • Poznan University of Physical Education, Faculty of Sport Sciences in Gorzow Wielkopolski, Poland; Department of Biological Sciences.
        • Contato:

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

  • Filho
  • Adulto

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • Female, aged 16-22 years.
  • Regular participation in organized basketball training.
  • Current medical clearance for sports participation.
  • No contraindications to high-intensity physical exercise.
  • Willingness and ability to provide written informed consent (and parental/legal guardian consent where required for minors).
  • Willingness to comply with all study procedures.
  • Menstrual cycle phase will be recorded for all participants and considered as a potential covariate in the statistical analyses.

Exclusion Criteria:

  • Current musculoskeletal injury or any condition preventing maximal exercise.
  • Metabolic, cardiovascular, inflammatory, or other chronic diseases affecting exercise capacity or study outcomes.
  • Current use of anti-inflammatory medications.
  • Use of supplements or substances that may influence the measured metabolic or inflammatory parameters.
  • Refusal to undergo blood sampling.
  • Failure to comply with pre-test instructions (e.g., dietary or exercise restrictions).

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: Outro
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: High-Intensity Interval Exercise (Yo-Yo IR1)
Participants assigned to this arm will complete a single session of the Yo-Yo Intermittent Recovery Test Level 1 (Yo-Yo IR1), a standardized high-intensity intermittent exercise protocol designed to simulate the physiological demands of competitive basketball. Assessments will be conducted before exercise, immediately after exercise, and one hour after exercise to evaluate acute metabolic, inflammatory, physiological, and fatigue-related responses.
The intervention consists of the Yo-Yo Intermittent Recovery Test Level 1 (Yo-Yo IR1), a standardized maximal intermittent field exercise test designed to reproduce the physiological demands of intermittent team sports such as basketball. Participants perform repeated 20-meter shuttle runs at progressively increasing speeds, guided by audio signals, with 10-second active recovery periods between running bouts. The test continues until volitional exhaustion or until the participant is unable to maintain the required running pace according to the test protocol. The Yo-Yo IR1 is used to induce acute physiological stress for the assessment of metabolic, inflammatory, and fatigue-related responses.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in Serum Interleukin-6 (IL-6) Concentration
Prazo: Baseline (pre-exercise), immediately after exercise, and 1 hour after exercise.
Serum interleukin-6 (IL-6) concentration will be measured to assess the acute inflammatory response induced by the Yo-Yo Intermittent Recovery Test Level 1 (Yo-Yo IR1). The outcome will be expressed as the change in IL-6 concentration across the predefined assessment time points.
Baseline (pre-exercise), immediately after exercise, and 1 hour after exercise.
Change in Blood Lactate Concentration
Prazo: Baseline and immediately after exercise.
Blood lactate concentration measured from capillary blood as an indicator of anaerobic metabolism following high-intensity intermittent exercise.
Baseline and immediately after exercise.
Change in reaction time
Prazo: Baseline and immediately post-exercise.
Visual reaction time will be assessed as an indicator of neuromotor performance and central fatigue.
Baseline and immediately post-exercise.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Change in serum-free fatty acid concentration
Prazo: Baseline, immediately post-exercise, and 1 hour post-exercise
Serum free fatty acid concentration will be measured from venous blood samples to evaluate exercise-induced lipid mobilization.
Baseline, immediately post-exercise, and 1 hour post-exercise
Change in blood glucose concentration
Prazo: Baseline, immediately post-exercise, and 1 hour post-exercise
Blood glucose concentration will be measured using a portable glucometer with disposable test strips.
Baseline, immediately post-exercise, and 1 hour post-exercise
Change in serum insulin concentration
Prazo: Baseline, immediately post-exercise, and 1 hour post-exercise
Serum insulin concentration will be measured to assess hormonal regulation of glucose metabolism.
Baseline, immediately post-exercise, and 1 hour post-exercise
Change in Rating of Perceived Exertion (Borg Scale)
Prazo: Immediately after exercise completion (within 5 minutes).
Subjective perception of exercise intensity will be assessed using the Borg Rating of Perceived Exertion Scale. Total scores range from 6 to 20, with higher scores indicating greater perceived exertion during exercise.
Immediately after exercise completion (within 5 minutes).
Change in mood state assessed by Profile of Mood States (POMS)
Prazo: Before exercise.
Mood state will be assessed using the validated Profile of Mood States questionnaire. Total scores range from 0 to 260, with higher scores indicating greater mood disturbance and psychological distress.
Before exercise.

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Anna Kasperska, PhD, Poznan University of Physical Education, Faculty of Sport Sciences in Gorzow Wielkopolski, Poland;

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Publicações Gerais

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)

20 de setembro de 2026

Conclusão Primária (Estimado)

30 de novembro de 2026

Conclusão do estudo (Estimado)

30 de dezembro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

3 de agosto de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

3 de agosto de 2026

Primeira postagem (Real)

7 de agosto de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

12 de agosto de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

11 de agosto de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • Basketball players
  • DGR.V.042.2.4.2026 (Número de outro subsídio/financiamento: Lubusz Voivodeship Marshal's Office and university funds.)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

Individual participant data collected during this study will not be made publicly available.

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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