Effect of Glenohumeral Internal Rotation Deficit on Shoulder Endurance and Stability in Adolescent Male Volleyball Players
The Effects of Glenohumeral Internal Rotation Deficit on Posterior Shoulder Endurance and Upper Extremity Stability in Adolescent Male Volleyball Players
1 other identifier
observational
52
1 country
1
Brief Summary
This study aims to investigate whether glenohumeral internal rotation deficit (GIRD) is associated with shoulder endurance and functional stability in male adolescent volleyball players aged 14 to 18 years who do not have shoulder pain. GIRD refers to a reduction in internal rotation range of motion of the dominant (spiking) shoulder compared with the non-dominant shoulder and is commonly observed in young athletes participating in overhead sports such as volleyball. Participants will be divided into two groups based on shoulder range of motion measurements. Athletes with a loss of at least 10 degrees of internal rotation in the dominant shoulder compared to the non-dominant shoulder will be classified as having GIRD, while those without this difference will be classified as not having GIRD. Shoulder internal and external rotation range of motion will be measured using standardized clinical assessment methods. Shoulder endurance and upper extremity functional stability will then be evaluated using clinically applicable performance-based tests, including the Shoulder Endurance Test, the Posterior Shoulder Endurance Test, and the Modified Closed Kinetic Chain Upper Extremity Stability Test. The results of these tests will be compared between athletes with and without GIRD. The main research question of this study is whether the presence of GIRD in asymptomatic adolescent volleyball players is associated with reduced shoulder muscle endurance and decreased functional stability of the upper extremity. The study hypothesizes that athletes with GIRD will demonstrate lower posterior shoulder endurance and poorer upper extremity stability compared to athletes without GIRD.
Trial Health
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participants targeted
Target at P25-P50 for all trials
Started Nov 2024
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 5, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 30, 2025
CompletedFirst Submitted
Initial submission to the registry
January 13, 2026
CompletedFirst Posted
Study publicly available on registry
January 28, 2026
CompletedJanuary 28, 2026
January 1, 2026
12 months
January 13, 2026
January 19, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Shoulder Endurance Test (SET) Duration
Shoulder endurance measured as time to volitional fatigue (seconds) during the Shoulder Endurance Test. Participants stand with the back against a wall and perform repeated movements from 90° shoulder flexion to 90° abduction with 90° external rotation and back, using a 1-m green TheraBand anchored to achieve \~100% elongation. Cadence is metronome-controlled and progressively increased (60 bpm, then 90, 120, and 150 bpm). Score range: 0 seconds to no upper limit; higher seconds indicate better endurance.
Through study completion, an average of 1 year
Secondary Outcomes (2)
Posterior Shoulder Endurance Test (PSET) Duration
through study completion, an average of 1 year
Modified Closed Kinetic Chain Upper Extremity Stability Test (Modified CKCUEST) Score
through study completion, an average of 1 year
Study Arms (2)
Glenohumeral internal rotation deficit (GIRD) Group
GIRD Present (≥10° internal rotation deficit)
Non-Glenohumeral internal rotation deficit (GIRD) Group
No GIRD (\<10° internal rotation deficit)
Interventions
Participants undergo a standardized shoulder assessment session. Glenohumeral internal and external rotation range of motion is measured using a goniometric clinical procedure with the shoulder positioned in standardized alignment. Functional performance is assessed using a battery of tests including a shoulder endurance test, a posterior shoulder endurance test, and a modified closed kinetic chain upper extremity stability test. All procedures are performed in a controlled laboratory setting by trained assessors following a consistent protocol.
Eligibility Criteria
The study population consists of adolescent male volleyball players aged 14-18 years with at least 3 years of licensed volleyball experience.
You may qualify if:
- Male adolescent volleyball players aged 14-18 years
- Be a licensed volleyball player for at least 3 years.
- Be male and currently without shoulder symptoms (no current shoulder complaint)
You may not qualify if:
- Signs of possible shoulder impingement: 3 or more positive results out of 5 clinical shoulder tests (Neer test, Hawkins-Kennedy test, Painful Arc test 60°-120°, infraspinatus weakness, Empty Can test)
- Shoulder pain within the last 6 months.
- A history of shoulder surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Physiotherapy and Rehabilitation, University of Health Sciences
Ankara, Ankara, 06010, Turkey (Türkiye)
Study Officials
- PRINCIPAL INVESTIGATOR
Seda Bicici Ulusahin, PhD
Saglik Bilimleri Universitesi
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator, PT PhD
Study Record Dates
First Submitted
January 13, 2026
First Posted
January 28, 2026
Study Start
November 5, 2024
Primary Completion
October 30, 2025
Study Completion
December 30, 2025
Last Updated
January 28, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share
No plan to share individual participant data (IPD) at this time