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Shoulder PainNCT07720050

Shoulder Pain, Core Endurance, and Scapular Control in Adolescent Volleyball Players

An observational study of Shoulder Pain and Scapular Dyskinesis, run by Istanbul Gelisim University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Shoulder pain is one of the most common musculoskeletal problems in adolescent volleyball players because of repetitive overhead activities such as serving and spiking. Although impaired scapular control and reduced core endurance have been suggested as potential contributors to shoulder pain, their combined… Read more about this study

Who is it for?
Ages 14 to 18 years, women onlyHealthy volunteers can take part
Conditions the study is for
Shoulder Pain, Scapular Dyskinesis, Core Endurance
What is being tested?
Visual Analog Scale (VAS), Scapular Dyskinesis Test and McGill Core Endurance Test Battery
How many people
60 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Mar 2026to 25 Jun 2026
How long will I take part?
1 Day
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 14 to 18 years
  • Women only
  • Healthy volunteers accepted
  • Child, Adult

Study population: Licensed female adolescent volleyball players aged 14-18 years who were actively participating in volleyball training at Nevşehir Youth and Sports Center and met the study eligibility criteria.

Who may be able to join

  • Female licensed volleyball players aged 14 to 18 years.
  • Participation in regular volleyball training at least three times per week.
  • Dominant upper extremity identified.
  • Ability to understand the study procedures and provide informed assent.
  • Written informed consent provided by a parent or legal guardian for participants younger than 18 years.

Who cannot join

  • Shoulder surgery within the previous 6 months.
  • Acute upper extremity or spinal injury.
  • History of fracture affecting the upper extremity or spine.
  • Neurological disorders affecting upper extremity function.
  • Systemic rheumatologic disease.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Istanbul Gelisim University

    Istanbul, Istanbul, 34310

Other trials in Turkey (Türkiye)

About this study

Official title: Investigation of the Relationship Between Shoulder Pain, Core Endurance, and Scapular Control in Adolescent Volleyball Players: A Cross-Sectional Study

Shoulder pain is one of the most common musculoskeletal problems in adolescent volleyball players because of repetitive overhead activities such as serving and spiking. Although impaired scapular control and reduced core endurance have been suggested as potential contributors to shoulder pain, their combined relationship has not been sufficiently investigated in young volleyball athletes.

This observational cross-sectional study aims to examine the relationship between shoulder pain, core endurance, and scapular control in licensed adolescent volleyball players aged 14 to 18 years. Participants with and without shoulder pain will undergo standardized assessments, including the Visual Analog Scale (VAS) for pain intensity, the Scapular Dyskinesis Test for scapular control, and the McGill Core Endurance Test Battery for trunk muscle endurance. The findings are expected to improve the understanding of factors associated with shoulder pain and contribute to the development of injury prevention and rehabilitation strategies for adolescent volleyball players.

Being tested
Visual Analog Scale (VAS), Scapular Dyskinesis Test, McGill Core Endurance Test Battery
Medical subject headings
Shoulder Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Visual Analog Scale (VAS)Diagnostic test

    Assessment of shoulder pain intensity using a 10-cm Visual Analog Scale.

  • Scapular Dyskinesis TestDiagnostic test

    Clinical assessment of scapular movement and control during repeated arm elevation.

  • McGill Core Endurance Test BatteryDiagnostic test

    Assessment of trunk muscle endurance using flexor, extensor, and lateral bridge endurance tests.

Study groups in NCT07720050
Study groupRoleWhat they receive
Shoulder Pain GroupLicensed adolescent volleyball players aged 14-18 years with shoulder pain. Participants underwent assessment of shoulder pain intensity using the Visual Analog Scale (VAS), scapular control using the Scapular Dyskinesis Test, and core muscle endurance using the McGill Core Endurance Test Battery.
Receives: Diagnostic Test: Visual Analog Scale (VAS); Diagnostic Test: Scapular Dyskinesis Test; Diagnostic Test: McGill Core Endurance Test Battery
Control GroupLicensed adolescent volleyball players aged 14-18 years without shoulder pain. Participants underwent the same standardized assessments, including the Visual Analog Scale (VAS), Scapular Dyskinesis Test, and McGill Core Endurance Test Battery.
Receives: Diagnostic Test: Visual Analog Scale (VAS); Diagnostic Test: Scapular Dyskinesis Test; Diagnostic Test: McGill Core Endurance Test Battery

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Core Muscle Endurance

    Core muscle endurance will be assessed using the McGill Core Endurance Test Battery, including trunk flexor, extensor, and bilateral side bridge endurance tests. Endurance time will be recorded in seconds.

    Measured: Baseline (Single assessment, Day 1)

Secondary outcomes (2)
  1. Scapular Control

    Scapular control will be evaluated using the Scapular Dyskinesis Test. The presence or absence of scapular dyskinesis will be recorded during repeated arm elevation.

    Measured: Baseline (Single assessment, Day 1)

  2. Shoulder Pain Intensity

    Shoulder pain intensity will be assessed using the 10-cm Visual Analog Scale (VAS). Scores range from 0 (no pain) to 10 (worst imaginable pain).

    Measured: Baseline (Single assessment, Day 1)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jul 2026
  2. Study start15 Mar 2026
  3. Primary completion20 Jun 2026
  4. Study completion25 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
60 participants (actual)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT07720050
Sponsor's protocol ID
NVS-SHOULDER-2026-01
Status last verified
Jul 2026
First submitted
18 Jul 2026
Last updated
22 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Shoulder Pain and Scapular Dyskinesis, run by Istanbul Gelisim University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Core Muscle Endurance (time frame: Baseline (Single assessment, Day 1)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jul 2026.

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