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.
Aperçu de l'étude
Statut
Les conditions
Type d'étude
Inscription (Estimé)
Contacts et emplacements
Lieux d'étude
-
-
Avcılar
-
Istanbul, Avcılar, Turquie (Türkiye), 34310
- Istanbul Gelisim University
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
Accepte les volontaires sains
Méthode d'échantillonnage
Population étudiée
La description
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.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
|
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.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Measuring the biomechanical properties of muscles with MyotonPro
Délai: 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
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Measuring the length of lower extremity using a tape measure.
Délai: 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
Délai: 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.
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- 27.04.2026-2026/04
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .