Reliability of Posterior Shoulder Endurance Test in Overhead Athletes

April 12, 2022 updated by: Damla Karabay, Dokuz Eylul University

Reliability of Posterior Shoulder Endurance Test in Overhead Athletes and Comparison of Athletes With and Without Shoulder Pain

The purpose of this study was to investigate the reliability of posterior shoulder endurance test in overhead athletes and to compare the endurance of posterior shoulder muscles between athletes with and without shoulder pain.

Study Overview

Status

Recruiting

Conditions

Detailed Description

A total of 40 overhead athletes, 20 with shoulder pain and 20 with no shoulder pain, will be included in the study. Shoulder endurance will be measured as isometric and isotonic on both arms of athletes using the posterior shoulder endurance test. The measurements will be repeated after 3-7 days, and the test-retest reliability of the isotonic and isometric posterior shoulder endurance test will be investigated.

Study Type

Observational

Enrollment (Anticipated)

40

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • İzmir
      • Balçova, İzmir, Turkey, 35340
        • Recruiting
        • Dokuz Eylul University, Sports Medicine department
        • Contact:
          • Damla KARABAY, MSc

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

11 years to 22 years (Child, Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Overhead athletes with and without shoulder pain

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

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

  • 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

This is where you will find people and organizations involved with this study.

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

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 31, 2019

Primary Completion (Anticipated)

September 30, 2022

Study Completion (Anticipated)

September 30, 2022

Study Registration Dates

First Submitted

December 11, 2019

First Submitted That Met QC Criteria

December 13, 2019

First Posted (Actual)

December 16, 2019

Study Record Updates

Last Update Posted (Actual)

April 13, 2022

Last Update Submitted That Met QC Criteria

April 12, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 4950-GOA

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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