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Muscle FatigueMAMFNCT07665008

MULTİDİMENSİONAL ASSESSMENT OF MUSCLE FATİGUE İN SOCCER PLAYERS

An observational study of Muscle Fatigue, run by Giresun University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Muscle fatigue is a multifactorial physiological phenomenon characterized by a reduction in the ability of a muscle to generate force during sustained or repetitive contractions. Read more about this study

Who is it for?
Ages 18 to 30 years, men onlyHealthy volunteers can take part
Conditions the study is for
Muscle Fatigue
What is being tested?
Neuromuscular Assessment Devices
Type of treatment
Medical device
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Nov 2024to 15 Mar 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 30 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Study population: Healthy male soccer players aged 18 to 30 years who were actively participating in regular football training and competition. Participants were recruited from football teams and underwent assessments of muscle thickness, surface electromyography (sEMG), accelerometer-derived mechanical vibration parameters, and isometric strength during laboratory-based testing sessions. Only individuals meeting all eligibility criteria and providing informed consent were included in the study.

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Ordu University Faculty of Sports Sciences

    Ordu, Merkez, 52100

Other trials in Turkey (Türkiye)

About this study

Official title: MULTIDIMENSIONAL ASSESSMENT OF MUSCLE FATIGUE USING ACCELEROMETER, ELECTROMYOGRAPHY AND MUSCLE THICKNESS DATA

Muscle fatigue is a multifactorial physiological phenomenon characterized by a reduction in the ability of a muscle to generate force during sustained or repetitive contractions. This cross-sectional observational study aimed to investigate the relationships among muscle thickness, surface electromyography (sEMG) median frequency, accelerometer-derived mechanical vibration parameters, and isometric force characteristics in healthy male soccer players. Thirty participants aged 18-30 years underwent ultrasonographic muscle thickness assessment, synchronized sEMG and accelerometer recordings, and isometric strength testing at different knee flexion angles (90°, 60°, and 30°). The study evaluated the interaction between morphological, electrical, and mechanical indicators of muscle fatigue to support the development of multidimensional fatigue monitoring approaches.

Read the 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.

Conditions
Muscle Fatigue
Being tested
Neuromuscular Assessment Devices
Keywords
Muscle Fatigue, Surface Electromyography, Accelerometry, Muscle Thickness, Mechanomyography

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Neuromuscular Assessment DevicesDevice

    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.

Study groups in NCT07665008
Study groupRoleWhat they receive
Healthy Male Soccer PlayersHealthy 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°).
Receives: Device: Neuromuscular Assessment Devices

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Surface Electromyography (sEMG) Median Frequency

    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.

    Measured: Day 1

Secondary outcomes (3)
  1. Muscle Thickness

    Ultrasonographic muscle thickness measurements of the VLO, VMO, and RFO muscles (mm).

    Measured: Day 1

  2. Accelerometer-Derived Mechanical Vibration Parameters

    Root mean square (RMS) acceleration values obtained from thigh and shank triaxial accelerometers during isometric contractions.

    Measured: Day 1

  3. Isometric Strength Parameters

    Peak torque, mean torque, and time-to-peak torque measured using an isokinetic dynamometer during maximal voluntary isometric contractions.

    Measured: Day 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jun 2026
  2. Study start1 Nov 2024
  3. Primary completion20 Feb 2025
  4. Study completion15 Mar 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07665008
Sponsor's protocol ID
TN-2024-127
Acronym
MAMF
Status last verified
Jun 2026
First submitted
12 Jun 2026
Last updated
24 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be publicly shared. The study was conducted as part of a doctoral thesis, and no formal data-sharing plan has been established. Aggregate study results are reported in publications, while access to underlying data may be considered by the corresponding author on a reasonable request basis and in accordance with applicable ethical and institutional requirements.

Publications

  • Karthick PA, Venugopal G, Ramakrishnan S. Analysis of Muscle Fatigue Progression using Cyclostationary Property of Surface Electromyography Signals. J Med Syst. 2016 Jan;40(1):28. doi: 10.1007/s10916-015-0394-0. Epub 2015 Nov 7.

    PubMed 26547848

Questions about this trial

What is this clinical trial studying?

An observational study of Muscle Fatigue, run by Giresun University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Surface Electromyography (sEMG) Median Frequency (time frame: Day 1). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07665008, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2026.

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