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

11 de agosto de 2026 actualizado 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.

Descripción general del estudio

Estado

Aún no reclutando

Descripción detallada

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 estudio

Intervencionista

Inscripción (Estimado)

25

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

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

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño
  • Adulto

Acepta Voluntarios Saludables

Sí

Descripción

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).

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Otro
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Serum Interleukin-6 (IL-6) Concentration
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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 resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in serum-free fatty acid concentration
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

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

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

20 de septiembre de 2026

Finalización primaria (Estimado)

30 de noviembre de 2026

Finalización del estudio (Estimado)

30 de diciembre de 2026

Fechas de registro del estudio

Enviado por primera vez

3 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

3 de agosto de 2026

Publicado por primera vez (Actual)

7 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de agosto de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

11 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • Basketball players
  • DGR.V.042.2.4.2026 (Otro número de subvención/financiamiento: Lubusz Voivodeship Marshal's Office and university funds.)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

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

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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