- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07425873
Differences in Shoulder Girdle Muscles in Young Swimmers
March 25, 2026 updated by: Istanbul Gelisim University
Examination of Differences in Shoulder Girdle Muscles in Young Swimmers According to Swimming Styles
This research aims to examine the effects of different swimming styles (freestyle, breaststroke, butterfly, and backstroke) on the characteristics of the shoulder girdle muscles in young swimmers.
Although it is known that shoulder girdle muscles undergo different levels of activation depending on swimming style, studies systematically examining these differences, especially in young swimmers during their developmental years, are limited.
Identifying style-based differences in shoulder girdle muscle activation is of great importance for both optimizing training programs and preventing injuries.
Study Overview
Status
Active, not recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
28
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Avcılar
-
Istanbul, Avcılar, Turkey (Türkiye), 34310
- Istanbul Gelisim University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Young swimmers
Description
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
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Breaststroke
|
MyotonPro is used to measure the biomechanical properties of muscle.
During measurements, participants will be seated in a chair with back support; 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 anterior, middle and posterior parts of the deltoid muscle and the upper, middle and lower parts of the trapezius muscle were measured using Myoton PRO.
All measurements will be compared statistically according to swimming styles.
The measuring tape will be used to measure the swimmers' Right and left arms length (cm) and Arm span (cm).
All measurements will be compared statistically according to swimming styles.
Passive range of motion of the upper 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 swimming styles.
|
|
Freestyle
|
MyotonPro is used to measure the biomechanical properties of muscle.
During measurements, participants will be seated in a chair with back support; 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 anterior, middle and posterior parts of the deltoid muscle and the upper, middle and lower parts of the trapezius muscle were measured using Myoton PRO.
All measurements will be compared statistically according to swimming styles.
The measuring tape will be used to measure the swimmers' Right and left arms length (cm) and Arm span (cm).
All measurements will be compared statistically according to swimming styles.
Passive range of motion of the upper 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 swimming styles.
|
|
Butterfly
|
MyotonPro is used to measure the biomechanical properties of muscle.
During measurements, participants will be seated in a chair with back support; 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 anterior, middle and posterior parts of the deltoid muscle and the upper, middle and lower parts of the trapezius muscle were measured using Myoton PRO.
All measurements will be compared statistically according to swimming styles.
The measuring tape will be used to measure the swimmers' Right and left arms length (cm) and Arm span (cm).
All measurements will be compared statistically according to swimming styles.
Passive range of motion of the upper 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 swimming styles.
|
|
Backstroke
|
MyotonPro is used to measure the biomechanical properties of muscle.
During measurements, participants will be seated in a chair with back support; 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 anterior, middle and posterior parts of the deltoid muscle and the upper, middle and lower parts of the trapezius muscle were measured using Myoton PRO.
All measurements will be compared statistically according to swimming styles.
The measuring tape will be used to measure the swimmers' Right and left arms length (cm) and Arm span (cm).
All measurements will be compared statistically according to swimming styles.
Passive range of motion of the upper 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 swimming styles.
|
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 measurements 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 anterior, middle and posterior parts of the deltoid muscle and the upper, middle and lower parts of the trapezius muscle were measured using Myoton PRO.
|
From enrollment to the end of measurements at 6 weeks.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measuring the length and range of motion of the upper 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 arms length (cm) and Arm span (cm).
|
From enrollment to the end of measurements at 6 weeks.
|
|
Measuring the length and range of motion of the upper extremity using a digital goniometer.
Time Frame: From enrollment to the end of measurements at 6 weeks.
|
Passive range of motion of the upper 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 (°)
|
From enrollment to the end of measurements at 6 weeks.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 12, 2025
Primary Completion (Estimated)
March 1, 2026
Study Completion (Estimated)
April 1, 2026
Study Registration Dates
First Submitted
January 27, 2026
First Submitted That Met QC Criteria
February 19, 2026
First Posted (Actual)
February 23, 2026
Study Record Updates
Last Update Posted (Actual)
March 27, 2026
Last Update Submitted That Met QC Criteria
March 25, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 29.12.2025-2025/12
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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