Effects of Core and Inspiratory Muscle Training on Muscle Oxygenation and Athletic Performance İn Young Soccer Players
1 other identifier
interventional
54
1 country
1
Brief Summary
The purpose of this randomized controlled trial is to investigate the effects of core training and inspiratory muscle training (IMT) on muscle oxygenation and athletic performance in youth male soccer players aged 15-18. A total of 54 healthy soccer players will be included and randomly assigned into three equal groups: the Control Group, the Core Training Group, and the Core Training + IMT Group. All interventions will be implemented for 8 weeks in addition to routine soccer training sessions. Assessments will be performed at baseline (Week 0), mid-intervention (Week 4), and post-intervention (Week 8). The primary outcome measures of the study are aerobic capacity assessed by the Yo-Yo Intermittent Recovery Test Level 1 and muscle oxygenation parameters monitored via near-infrared spectroscopy (NIRS) using a MOXY monitor. Secondary outcome measures include sprint performance, agility, dynamic balance, core muscle strength and endurance, inspiratory muscle strength, lower extremity explosive power, and soccer-specific technical performance tests. Overall, this study aims to reveal the combined effects of core training and inspiratory muscle training on muscle oxygenation, respiratory functions, aerobic capacity, and soccer performance, while explaining the underlying physiological mechanisms in youth athletes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 15, 2026
CompletedFirst Posted
Study publicly available on registry
June 18, 2026
CompletedStudy Start
First participant enrolled
August 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2027
June 18, 2026
June 1, 2026
1 year
June 15, 2026
June 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Aerobic Capacity
Assessed using the Yo-Yo Intermittent Recovery Test Level 1 (Yo-Yo IR1) to determine the total distance covered in meters.
Baseline (Week 0), Mid-intervention (Week 4), and Post-intervention (Week 8)
Muscle Oxygen Saturation (SmO2)
Measured in percentage (%) during exercise using near-infrared spectroscopy (NIRS) via a MOXY monitor to evaluate muscle oxygenation.
Baseline (Week 0), Mid-intervention (Week 4), and Post-intervention (Week 8)
Total Hemoglobin (THb)
Measured in arbitrary units or micro-molar concentrations using a MOXY monitor (NIRS technology) to assess local blood volume changes and muscle hemodynamics.
Baseline (Week 0), Mid-intervention (Week 4), and Post-intervention (Week 8)
Secondary Outcomes (8)
20-Meter Sprint Performance
Baseline (Week 0), Mid-intervention (Week 4), and Post-intervention (Week 8)
Agility Performance
Baseline (Week 0), Mid-intervention (Week 4), and Post-intervention (Week 8)
Dynamic Balance
Baseline (Week 0), Mid-intervention (Week 4), and Post-intervention (Week 8)
Core Muscle Strength and Endurance
Baseline (Week 0), Mid-intervention (Week 4), and Post-intervention (Week 8)
Lower Extremity Explosive Power
Baseline (Week 0), Mid-intervention (Week 4), and Post-intervention (Week 8)
- +3 more secondary outcomes
Study Arms (3)
Control Group
NO INTERVENTIONParticipants in this group will only continue their routine soccer training program for 8 weeks without any additional core or respiratory intervention.
Core Training Group
EXPERIMENTALParticipants will perform a structured core training program in addition to their routine soccer training. The intervention will be conducted 3 days a week for 8 weeks, taking approximately 20-25 minutes before soccer practices, using a progressive overload principle.
Combined Training Group
EXPERIMENTALParticipants will receive both the structured core training program and inspiratory muscle training (IMT) in addition to routine soccer training. Core training will be done 3 days a week for 20-25 minutes. IMT will be performed 3 days a week using a threshold device (2 sets of 30 breaths), starting at 50% of maximal inspiratory pressure (MIP) and progressing to 70% over 8 weeks.
Interventions
A structured, progressive core stability training program targeting trunk and abdominal musculature. The exercises will be conducted 3 days a week for 8 weeks, taking approximately 20-25 minutes before soccer practices.
Inspiratory muscle training performed using a threshold device. The protocol consists of 2 sets of 30 breaths per session, 3 days a week for 8 weeks. Training intensity starts at 50% of maximal inspiratory pressure (MIP) and progresses up to 70% MIP.
Eligibility Criteria
You may qualify if:
- Being between 15 and 18 years of age.
- Being a male soccer player.
- Actively and regularly participating in trainings at Alagöz Soccer Club.
- Having participated in regular soccer training for at least the last 6 months.
- Being able to continue routine trainings throughout the study period.
- Being fully informed about the research.
- Having obtained voluntary informed consent, and parental/guardian consent for participants under 18 years of age.
- Having the cognitive and physical capacity to understand and fulfill the specific test and exercise instructions.
You may not qualify if:
- Having a history of lower extremity, trunk-core, or athletic performance-limiting injury within the last 6 months.
- Having undergone orthopedic lower extremity or spine surgery within the last 1 year.
- Having active musculoskeletal pain or any orthopedic/neurological condition that prevents exercise.
- Having any health condition that prevents the safe execution of balance, sprint, agility, jump, or core endurance tests.
- Having asthma, chronic respiratory system diseases, exercise-induced bronchospasm, cardiovascular disease, or a physician-imposed restriction on high-intensity exercise that could affect respiratory muscle or exercise testing.
- Having open wounds, infections, or severe skin sensitivity that prevents the application of sensors placed on the skin.
- Currently participating in another structured respiratory muscle training or structured core exercise program that could affect the study results.
- Having a body mass index (BMI) of 30 kg/m² or above.
- Being deemed unsuitable for the study by the researcher due to safety concerns.
- Withdrawal from the study at the request of the participant or their parent/guardian.
- Missing two consecutive exercise sessions or having an insufficient overall attendance rate.
- Developing an exercise-preventing injury or illness during the study period.
- Occurrence of any safety risk during testing or exercise sessions.
- Non-compliance with the study protocol.
- Starting another additional exercise program during the study.
- +1 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Igdir University
Iğdır, 76000, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Abdurrahim Eyüp CANBALOĞLU, MSc
IĞDIR UNİVERSİTY
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant & PhD Student
Study Record Dates
First Submitted
June 15, 2026
First Posted
June 18, 2026
Study Start
August 1, 2026
Primary Completion (Estimated)
August 1, 2027
Study Completion (Estimated)
December 1, 2027
Last Updated
June 18, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared with third parties to ensure the confidentiality and privacy of the participants, in accordance with the informed consent limitations and ethical committee guidelines.