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Active, not recruitingNCT07621913Updated Jun 2, 2026

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

An observational study in Lower Extremity Muscles Biomechanical Properties and Joint Range of Motion in Swimmers, sponsored by Istanbul Gelisim University. Active, not recruiting at 1 site in Turkey (Türkiye). Open to participants aged 12 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-02.

Sponsored by Istanbul Gelisim University · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2026, 3 months ago, but the record still lists the study as active, not recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
42
Ages
12 Years to 18 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Lower Extremity Muscles Biomechanical Properties and Joint Range of Motion in Swimmers
03

In context

Lead sponsor

Istanbul Gelisim University is the lead sponsor of 59 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Young healthy swimmers

Eligibility criteria

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.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
42 participants (estimated)
Patient registry
No

Groups and cohorts

  • Monofin swimmers

    Device: Measuring of the biomechanical properties of muscles with MyotonPro · Device: Measurement of the length of the lower extremity with a tape measure. · Device: Measuring the range of motion of the lower extremity joints with a digital goniometer

  • Bi-fin swimmers

    Device: Measuring of the biomechanical properties of muscles with MyotonPro · Device: Measurement of the length of the lower extremity with a tape measure. · Device: Measuring the range of motion of the lower extremity joints with a digital goniometer

Interventions

  • DeviceMeasuring of the biomechanical properties of muscles with MyotonPro

    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.

  • DeviceMeasurement of the length of the lower extremity with a tape measure.

    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.

  • DeviceMeasuring the range of motion of the lower extremity joints with a digital goniometer

    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.

06

What researchers measure

Primary outcomes

  1. Measuring the biomechanical properties of muscles with MyotonPro

    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.

    Time frame: From enrollment to the end of treatment at 6 weeks

Secondary outcomes

  1. Measuring the length of lower extremity using a tape measure.

    The measuring tape will be used to measure the swimmers' Right and left legs length (cm).

    Time frame: From enrollment to the end of measurements at 6 weeks.

  2. Measuring the range of motion of the lower extremity using a digital goniometer

    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 (°)

    Time frame: From enrollment to the end of 6 weeks.

07

Study locations

1 site
  • Istanbul Gelisim University
    Istanbul, Avcılar 34310, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07621913
Lead sponsor
Istanbul Gelisim University
Responsible party
Sponsor
First posted
Jun 2, 2026
Start date
May 2, 2026
Primary completion
Jun 15, 2026 (estimated)
Completion
Jun 30, 2026 (estimated)
Last update
Jun 2, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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