- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico 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.
Visão geral do estudo
Status
Tipo de estudo
Inscrição (Estimado)
Contactos e Locais
Locais de estudo
-
-
Avcılar
-
Istanbul, Avcılar, Turquia (Türkiye), 34310
- Istanbul Gelisim University
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Filho
- Adulto
Aceita Voluntários Saudáveis
Método de amostragem
População do estudo
Descrição
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.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
Coortes e Intervenções
Grupo / Coorte |
Intervenção / Tratamento |
|---|---|
|
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.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Measuring the biomechanical properties of muscles with MyotonPro
Prazo: 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 resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Measuring the length of lower extremity using a tape measure.
Prazo: 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
Prazo: 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
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Outros números de identificação do estudo
- 27.04.2026-2026/04
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .