- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07621913
Comparison of Lower Extremity Parameters in Monofin and Bi-fin Swimmers.
Comparison of Lower Extremity Muscle Biomechanical Properties, Joint Range of Motion, and Performance Parameters in Monofin and Bi-fin Swimmers
The purpose of this study is to compare the leg muscle features and joint movements of swimmers who use a single large fin (monofin) versus those who use two fins (bi-fins). Different types of fins change how legs move in the water. This may affect the muscle structure and swimming performance. The researchers want to find out the differences between these two groups of swimmers.
During the study, the researchers will do the following:
Record the age, height, and weight of healthy swimmers who train regularly. Measure the stiffness and flexibility of the leg muscles using MyotonPro device.
Check how well the hips, knees, and ankles can move using digital goniometer.
The findings from this study will help create safer training programs for swimmers. Coaches will use the results to improve swimming performance and lower the risk of leg injuries.
Panoramica dello studio
Stato
Tipo di studio
Iscrizione (Stimato)
Contatti e Sedi
Luoghi di studio
-
-
Avcılar
-
Istanbul, Avcılar, Turchia (Türkiye), 34310
- Istanbul Gelisim University
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Bambino
- Adulto
Accetta volontari sani
Metodo di campionamento
Popolazione di studio
Descrizione
Inclusion Criteria:
- Inclusion Criteria:
- Being between 12-18 years old
- Having been involved in at least one swimming style for at least 3 years
- Having participated in at least one competition
- Obtaining parental consent. Obtaining parental consent.
Exclusion Criteria:
- - Having undergone any surgery on the shoulder girdle muscles.
- Having any orthopedic or physical disorder in the shoulder girdle muscles (e.g., frozen shoulder).
- Participating in another sport besides swimming.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
Coorti e interventi
Gruppo / Coorte |
Intervento / Trattamento |
|---|---|
|
Monofin swimmers
|
MyotonPro is used to utilize the biomechanical properties of the muscle.
During measurements, the patient will be seated in a chair with back support; the biomechanical properties of the rectus femoris, tibialis anterior, medial gastrocnemius, and hamstring muscles (F - Natural Oscillation Frequency [Hz], Tone or Tension ranges, S - Dynamic Stiffness [N/m], D - Logarithmic Decrease [relative unit], Elasticity increase, R - Mechanical Stress Relaxation Time [ms], C - Relaxation and Deformation Time Ratio [relaxation and deformation time ratio [N/m]) will be measured bilaterally using Myoton PRO.
All measurements will be tracked according to the mileage.
Swimmers' right and left leg lengths (cm) will be measured.
All measurements will be tracked in terms of kilometers covered.
All measurements will be compared statistically according to pallet types.
Passive range of motion of the lower extremity shoulder joint (flexion, extension, adduction, abduction, external rotation, and internal rotation) will be measured using a digital goniometer.
Results will be recorded in degrees (°).
All measurements will be compared statistically according to pallet types.
|
|
Bi-fin swimmers
|
MyotonPro is used to utilize the biomechanical properties of the muscle.
During measurements, the patient will be seated in a chair with back support; the biomechanical properties of the rectus femoris, tibialis anterior, medial gastrocnemius, and hamstring muscles (F - Natural Oscillation Frequency [Hz], Tone or Tension ranges, S - Dynamic Stiffness [N/m], D - Logarithmic Decrease [relative unit], Elasticity increase, R - Mechanical Stress Relaxation Time [ms], C - Relaxation and Deformation Time Ratio [relaxation and deformation time ratio [N/m]) will be measured bilaterally using Myoton PRO.
All measurements will be tracked according to the mileage.
Swimmers' right and left leg lengths (cm) will be measured.
All measurements will be tracked in terms of kilometers covered.
All measurements will be compared statistically according to pallet types.
Passive range of motion of the lower extremity shoulder joint (flexion, extension, adduction, abduction, external rotation, and internal rotation) will be measured using a digital goniometer.
Results will be recorded in degrees (°).
All measurements will be compared statistically according to pallet types.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Measuring the biomechanical properties of muscles with MyotonPro
Lasso di tempo: From enrollment to the end of treatment at 6 weeks
|
Bilaterally Biomechanical properties (F - Natural Oscillation Frequency [Hz], characterizing Tone or Tension, S - Dynamic Stiffness [N/m], D - Logarithmic Decrement [relative unit], characterizing Elasticity, R - Mechanical Stress Relaxation Time [ms], C - Ratio of Relaxation and Deformation time [relative unit], characterizing Creep) of the rectus femoris, tibialis anterior, medial gastrocnemius and hamstring muscles were measured using Myoton PRO. Because the MyotonPRO assessment yields a single-session composite outcome by presenting all relevant units concurrently on the screen, these variables were treated as a whole rather than being documented separately. |
From enrollment to the end of treatment at 6 weeks
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Measuring the length of lower extremity using a tape measure.
Lasso di tempo: From enrollment to the end of measurements at 6 weeks.
|
The measuring tape will be used to measure the swimmers' Right and left legs length (cm).
|
From enrollment to the end of measurements at 6 weeks.
|
|
Measuring the range of motion of the lower extremity using a digital goniometer
Lasso di tempo: From enrollment to the end of 6 weeks.
|
Passive range of motion of the lower extremity joints (flexion, extension, adduction, abduction, external rotation, and internal rotation) will be measured using a digital goniometer.
Results will be recorded in degrees (°)
|
From enrollment to the end of 6 weeks.
|
Collaboratori e investigatori
Sponsor
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Altri numeri di identificazione dello studio
- 27.04.2026-2026/04
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .