- ICH GCP
- US Clinical Trials Registry
- Clinical Trial 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.
Study Overview
Status
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
Avcılar
-
Istanbul, Avcılar, Turkey (Türkiye), 34310
- İstanbul Gelisim University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measuring the biomechanical properties of muscles with MyotonPro
Time Frame: 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
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measuring the length of lower extremity using a tape measure.
Time Frame: 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
Time Frame: 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.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 27.04.2026-2026/04
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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