- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07665008
MULTİDİMENSİONAL ASSESSMENT OF MUSCLE FATİGUE İN SOCCER PLAYERS (MAMF)
MULTIDIMENSIONAL ASSESSMENT OF MUSCLE FATIGUE USING ACCELEROMETER, ELECTROMYOGRAPHY AND MUSCLE THICKNESS DATA
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Muscle fatigue is commonly assessed using surface electromyography (sEMG), particularly through frequency-domain parameters such as median frequency. However, fatigue-related changes are not limited to electrical activity and may also involve alterations in muscle mechanical behavior and morphological characteristics. Accelerometer-derived signals provide information regarding muscle vibrations and mechanical oscillations, while ultrasonographic measurements of muscle thickness provide information about muscle morphology and force-generating capacity.
The purpose of this study was to examine the relationships among muscle thickness, sEMG median frequency, accelerometer-derived mechanical vibration parameters, and isometric force variables during maximal voluntary isometric contractions performed at different knee flexion angles. Healthy male soccer players participated in a laboratory-based assessment protocol including ultrasonography, synchronized sEMG recordings, triaxial accelerometry, and isokinetic dynamometry.
Muscle thickness of the vastus lateralis obliquus (VLO), vastus medialis obliquus (VMO), and rectus femoris obliquus (RFO) muscles was measured using ultrasonography. Participants subsequently performed maximal voluntary isometric contractions at 90°, 60°, and 30° knee flexion angles. Surface electromyography, accelerometer signals, and force-related variables were recorded simultaneously. Median frequency values, acceleration-based root mean square (RMS) parameters, peak torque, mean torque, and time-to-peak torque variables were analyzed.
The study aimed to provide a multidimensional framework for muscle fatigue assessment by integrating morphological, electrical, and mechanical indicators and to explore their associations in healthy athletic populations.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Merkez
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Ordu, Merkez, Turkey (Türkiye), 52100
- Ordu University Faculty of Sports Sciences
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Healthy male soccer players aged 18-30 years
- No lower extremity injury within the previous six months
- No condition limiting lower extremity exercise performance
- No caffeine or stimulant consumption on the testing day
- Non-smoker
- Provided written informed consent
Exclusion Criteria:
- Female athletes
- Serious injury to the dominant leg within the previous year
- Intense exercise within the previous 24 hours
- Use of pain relievers or muscle relaxants on the testing day
- Inability to complete testing procedures
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Healthy Male Soccer Players
Healthy male soccer players aged 18-30 years who participated in a cross-sectional observational study.
Participants underwent ultrasonographic muscle thickness assessment, surface electromyography (sEMG), accelerometer-based mechanical vibration measurements, and isometric strength testing during maximal voluntary isometric contractions performed at different knee flexion angles (30°, 60°, and 90°).
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Participants underwent non-invasive neuromuscular assessment procedures using surface electromyography (sEMG), triaxial accelerometers, ultrasonography, and an isokinetic dynamometer.
Measurements were performed during maximal voluntary isometric contractions at 30°, 60°, and 90° knee flexion angles.
The devices were used exclusively for data collection and assessment purposes.
No therapeutic, pharmacological, behavioral, or rehabilitative intervention was administered.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Surface Electromyography (sEMG) Median Frequency
Time Frame: Day 1
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Median frequency (Hz) obtained from the vastus lateralis obliquus (VLO), vastus medialis obliquus (VMO), and rectus femoris obliquus (RFO) muscles during maximal voluntary isometric contractions performed at 30°, 60°, and 90° knee flexion angles.
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Day 1
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle Thickness
Time Frame: Day 1
|
Ultrasonographic muscle thickness measurements of the VLO, VMO, and RFO muscles (mm).
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Day 1
|
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Accelerometer-Derived Mechanical Vibration Parameters
Time Frame: Day 1
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Root mean square (RMS) acceleration values obtained from thigh and shank triaxial accelerometers during isometric contractions.
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Day 1
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Isometric Strength Parameters
Time Frame: Day 1
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Peak torque, mean torque, and time-to-peak torque measured using an isokinetic dynamometer during maximal voluntary isometric contractions.
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Day 1
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Tuğçe Namazcı, PhD, Giresun Üniversitesi
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- TN-2024-127
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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