Physiological Responses to Basketball-Specific Interval Exercise in Female Basketball Players

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age16-22
SponsorPoznan University of Physical Education

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Female, aged 16-22 years.

Regular participation in organized basketball training.

Current medical clearance for sports participation.

No contraindications to high-intensity physical exercise.

Disqualifiers

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.

Trial design

Design model

Single group

Treatments tested in this trial

  • Yo-Yo Intermittent Recovery Test Level 1 (Yo-Yo IR1)

    Other intervention

    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.

Treatment groups

25 Participants
are divided into 1 treatment group
Group A: High-Intensity Interval Exercise (Yo-Yo IR1)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in Serum Interleukin-6 (IL-6) Concentration

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.

Time frame
Baseline (pre-exercise), immediately after exercise, and 1 hour after exercise.
2

Change in Blood Lactate Concentration

Blood lactate concentration measured from capillary blood as an indicator of anaerobic metabolism following high-intensity intermittent exercise.

Time frame
Baseline and immediately after exercise.
3

Change in reaction time

Visual reaction time will be assessed as an indicator of neuromotor performance and central fatigue.

Time frame
Baseline and immediately post-exercise.

Secondary outcomes

1

Change in serum-free fatty acid concentration

Serum free fatty acid concentration will be measured from venous blood samples to evaluate exercise-induced lipid mobilization.

Time frame
Baseline, immediately post-exercise, and 1 hour post-exercise
2

Change in blood glucose concentration

Blood glucose concentration will be measured using a portable glucometer with disposable test strips.

Time frame
Baseline, immediately post-exercise, and 1 hour post-exercise
3

Change in serum insulin concentration

Serum insulin concentration will be measured to assess hormonal regulation of glucose metabolism.

Time frame
Baseline, immediately post-exercise, and 1 hour post-exercise
4

Change in Rating of Perceived Exertion (Borg Scale)

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.

Time frame
Immediately after exercise completion (within 5 minutes).

Other outcomes

Sponsors and contacts

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