- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04199988
Reliability of Posterior Shoulder Endurance Test in Overhead Athletes
Reliability of Posterior Shoulder Endurance Test in Overhead Athletes and Comparison of Athletes With and Without Shoulder Pain
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Damla KARABAY, PhD
- Phone Number: +902323293535
- Email: damla.karabay@yahoo.com
Study Locations
-
-
İzmir
-
Balçova, İzmir, Turkey, 35340
- Recruiting
- Dokuz Eylul University, Sports Medicine department
-
Contact:
- Damla KARABAY, MSc
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
For all athletes:
- Being between the ages of 13-24,
- Participating to overhead sports (tennis, volleyball, handball, etc.),
- Training at least 2-3 hours a week,
- Active participation in training and competitions,
- To be able to complete all assessments in the study,
For athletes with shoulder pain:
- Shoulder pain is 3/10 or more in the Visual Analogue Scale.
For Athletes without shoulder pain:
- No shoulder pain (0/10 according to Visual Analog Scale)
- No history of a shoulder injury and/or shoulder symptoms requiring treatment for the past 1 year.
- Having 90/100 or higher results in Kerlan-Jobe Orthopedic Clinical Shoulder & Elbow Score
Exclusion Criteria:
- Bilateral shoulder pain,
- Upper extremity fracture history,
- Surgical history of shoulder, cervical and thoracic region,
- Diagnosis of musculoskeletal disease in the cervical region, elbow, and wrist,
- Neck and shoulder pain with active/passive cervical spine movement,
- Frozen shoulder,
- Multidirectional joint hypermobility,
- Having a systemic musculoskeletal disease,
- Diagnosis of chest deformity and scoliosis.
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Athletes with shoulder pain
Overhead athletes with shoulder pain
|
Isometric posterior shoulder endurance test: In the prone position, the athlete's shoulder will be placed at horizontal abduction, and the time for maintaining this position will be recorded. Isotonic shoulder endurance test: In the prone position, the athlete's shoulder will be placed at horizontal abduction and asked to perform horizontal adduction-abduction, and the athlete will horizontally abducted-adducted his/her arm to 90 degrees at a cadence of 30 beats per minute. The number of repetitions will be recorded. |
Athletes without shoulder pain
Overhead athletes without shoulder pain
|
Isometric posterior shoulder endurance test: In the prone position, the athlete's shoulder will be placed at horizontal abduction, and the time for maintaining this position will be recorded. Isotonic shoulder endurance test: In the prone position, the athlete's shoulder will be placed at horizontal abduction and asked to perform horizontal adduction-abduction, and the athlete will horizontally abducted-adducted his/her arm to 90 degrees at a cadence of 30 beats per minute. The number of repetitions will be recorded. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Isometric Posterior Shoulder Endurance Test
Time Frame: Measurements will be performed in two sessions (3 to 7 days)
|
Isometric
|
Measurements will be performed in two sessions (3 to 7 days)
|
Isotonic Posterior Shoulder Endurance Test
Time Frame: Measurements will be performed in two sessions (3 to 7 days)
|
Isotonic
|
Measurements will be performed in two sessions (3 to 7 days)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sevgi Sevi Yeşilyaprak, PhD, Dokuz Eylül University
- Study Chair: Birsu TOPÇUGİL KIRIK, MD, Dokuz Eylül University
- Study Chair: Oğuz YÜKSEL, MD, Dokuz Eylül University
- Study Chair: Oğuzcan GÖKÇAY, MD, Dokuz Eylül University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 4950-GOA
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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