- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07720050
Shoulder Pain, Core Endurance, and Scapular Control in Adolescent Volleyball Players
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.
Studienübersicht
Status
Bedingungen
Studientyp
Einschreibung (Tatsächlich)
Kontakte und Standorte
Studienorte
-
-
Istanbul
-
Istanbul, Istanbul, Türkei (türkiye), 34310
- Istanbul Gelisim University
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Kind
- Erwachsene
Akzeptiert gesunde Freiwillige
Probenahmeverfahren
Studienpopulation
Beschreibung
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
Kohorten und Interventionen
Gruppe / Kohorte |
Intervention / Behandlung |
|---|---|
|
Shoulder Pain Group
Licensed 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.
|
Assessment of shoulder pain intensity using a 10-cm Visual Analog Scale.
Clinical assessment of scapular movement and control during repeated arm elevation.
Assessment of trunk muscle endurance using flexor, extensor, and lateral bridge endurance tests.
|
|
Control Group
Licensed 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.
|
Assessment of shoulder pain intensity using a 10-cm Visual Analog Scale.
Clinical assessment of scapular movement and control during repeated arm elevation.
Assessment of trunk muscle endurance using flexor, extensor, and lateral bridge endurance tests.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Core Muscle Endurance
Zeitfenster: Baseline (Single assessment, Day 1)
|
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.
|
Baseline (Single assessment, Day 1)
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Scapular Control
Zeitfenster: Baseline (Single assessment, Day 1)
|
Scapular control will be evaluated using the Scapular Dyskinesis Test.
The presence or absence of scapular dyskinesis will be recorded during repeated arm elevation.
|
Baseline (Single assessment, Day 1)
|
|
Shoulder Pain Intensity
Zeitfenster: Baseline (Single assessment, Day 1)
|
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).
|
Baseline (Single assessment, Day 1)
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- NVS-SHOULDER-2026-01
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .