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Comparison of Lower Extremity Parameters in Monofin and Bi-fin Swimmers.

1 de junio de 2026 actualizado por: Istanbul Gelisim University

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.

Descripción general del estudio

Tipo de estudio

De observación

Inscripción (Estimado)

42

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Avcılar
      • Istanbul, Avcılar, Turquía (Türkiye), 34310
        • Istanbul Gelisim University

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño
  • Adulto

Acepta Voluntarios Saludables

Sí

Método de muestreo

Muestra de probabilidad

Población de estudio

Young healthy swimmers

Descripción

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 de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Measuring the biomechanical properties of muscles with MyotonPro
Periodo de tiempo: 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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Measuring the length of lower extremity using a tape measure.
Periodo de tiempo: 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
Periodo de tiempo: 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.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

2 de mayo de 2026

Finalización primaria (Estimado)

15 de junio de 2026

Finalización del estudio (Estimado)

30 de junio de 2026

Fechas de registro del estudio

Enviado por primera vez

20 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

1 de junio de 2026

Publicado por primera vez (Actual)

2 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

2 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

1 de junio de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 27.04.2026-2026/04

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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