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

11 augustus 2026 bijgewerkt door: 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.

Studie Overzicht

Toestand

Nog niet aan het werven

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Geschat)

25

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Contact Back-up

Studie Locaties

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

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Kind
  • Volwassen

Accepteert gezonde vrijwilligers

Ja

Beschrijving

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).

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Ander
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in Serum Interleukin-6 (IL-6) Concentration
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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.

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in serum-free fatty acid concentration
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

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

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

20 september 2026

Primaire voltooiing (Geschat)

30 november 2026

Studie voltooiing (Geschat)

30 december 2026

Studieregistratiedata

Eerst ingediend

3 augustus 2026

Eerst ingediend dat voldeed aan de QC-criteria

3 augustus 2026

Eerst geplaatst (Werkelijk)

7 augustus 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

12 augustus 2026

Laatste update ingediend die voldeed aan QC-criteria

11 augustus 2026

Laatst geverifieerd

1 augustus 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • Basketball players
  • DGR.V.042.2.4.2026 (Ander subsidie-/financieringsnummer: Lubusz Voivodeship Marshal's Office and university funds.)

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

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

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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