- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07642310
Effects of ShoulderSphere Exercises in Young Adults
Effects of ShoulderSphere Exercises on Shoulder Stabilization, Strength, Proprioception, and Endurance in Young Adults
This study evaluated the effects of ShoulderSphere exercises on shoulder stability, muscle strength, proprioception, endurance, and functional performance in young adults.
ShoulderSphere is an exercise device that provides dynamic and multi-directional resistance during shoulder movements. The study compared an 8-week ShoulderSphere-based exercise program with a conventional shoulder stabilization exercise program based on selected Thrower's Ten exercises.
Young adults without current shoulder symptoms were included in the study. Participants were assigned to one of two exercise groups. Shoulder stability, functional upper-extremity performance, shoulder proprioception, and isokinetic muscle strength and endurance were assessed before and after the 8-week intervention.
The aim of the study was to determine whether ShoulderSphere exercises produced different effects compared with conventional shoulder stabilization exercises in young adults.
Studienübersicht
Status
Detaillierte Beschreibung
This study was designed as a controlled pretest-posttest intervention study in young adults. The purpose was to compare the effects of an 8-week ShoulderSphere-based exercise program with a conventional shoulder stabilization exercise program based on selected Thrower's Ten exercises.
Participants were young adults between 18 and 40 years of age who did not have current shoulder pain or clinical shoulder symptoms. Participants were assigned to either the ShoulderSphere exercise group or the conventional exercise group.
The ShoulderSphere group performed exercises using the ShoulderSphere device, which provides dynamic resistance and requires continuous control of shoulder movement. The conventional exercise group performed selected shoulder stabilization exercises based on the Thrower's Ten program. Both interventions were applied for 8 weeks.
Outcome assessments were performed before and after the intervention period. Shoulder stability was assessed using the Closed Kinetic Chain Upper Extremity Stability Test. Functional upper-extremity performance was assessed using the seated single-arm medicine ball throw test. Shoulder proprioception was assessed using an active joint position sense test. Isokinetic shoulder muscle strength and endurance were assessed using an isokinetic dynamometer.
The main purpose of the study was to examine whether ShoulderSphere exercises had different effects from conventional shoulder stabilization exercises on shoulder stability, strength, proprioception, endurance, and functional performance in young adults.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
-
Ankara, Türkei (türkiye), 06540
- Gazi University Graduate School of Health Sciences
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Being between 18 and 40 years of age
- Having no current shoulder pain or clinical shoulder symptoms
- Meeting the study screening criterion for shoulder stability based on the Closed Kinetic Chain Upper Extremity Stability Test
- Volunteering to participate in the study
- Providing written informed consent
Exclusion Criteria:
- Having current shoulder pain or any clinical shoulder symptoms
- Having a history of shoulder surgery
- Having a history of shoulder dislocation, subluxation, or significant shoulder trauma
- Having any neurological, rheumatological, or systemic condition that could affect upper-extremity function
- Having an acute musculoskeletal injury affecting the shoulder, neck, back, or upper extremity
- Having any condition that would prevent safe participation in the exercise program or outcome assessments
- Unable to complete the intervention or assessment procedures
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Sonstiges
- Zuteilung: Nicht randomisiert
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: ShoulderSphere Exercise Group
Participants in this arm performed an 8-week ShoulderSphere-based shoulder exercise program.
The exercises were performed using the ShoulderSphere device and aimed to improve shoulder stability, proprioception, muscle strength, endurance, and functional upper-extremity performance.
|
Participants performed an 8-week shoulder exercise program using the ShoulderSphere device.
The program aimed to improve shoulder stability, proprioception, muscle strength, endurance, and functional upper-extremity performance through dynamic and multi-directional shoulder control exercises.
|
|
Aktiver Komparator: Conventional Shoulder Stabilization Exercise Group
Participants in this arm performed an 8-week conventional shoulder stabilization exercise program based on selected Thrower's Ten exercises.
The exercises aimed to improve shoulder stability, proprioception, muscle strength, endurance, and functional upper-extremity performance.
|
Participants performed an 8-week conventional shoulder stabilization exercise program based on selected Thrower's Ten exercises.
The program aimed to improve shoulder stability, proprioception, muscle strength, endurance, and functional upper-extremity performance.
Andere Namen:
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Change in shoulder stability from baseline to 8 weeks
Zeitfenster: Baseline and 8 weeks
|
Shoulder stability was assessed using the Closed Kinetic Chain Upper Extremity Stability Test.
The number of touches completed during the test was recorded before and after the 8-week intervention period.
|
Baseline and 8 weeks
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Change in functional upper-extremity performance from baseline to 8 weeks
Zeitfenster: Baseline and 8 weeks
|
Functional upper-extremity performance was assessed using the seated single-arm medicine ball throw test.
The throwing distance was recorded before and after the 8-week intervention period.
|
Baseline and 8 weeks
|
|
Change in shoulder proprioception from baseline to 8 weeks
Zeitfenster: Baseline and 8 weeks
|
Shoulder proprioception was assessed using an active joint position sense test for internal and external rotation.
Absolute error values were recorded before and after the 8-week intervention period.
|
Baseline and 8 weeks
|
|
Change in isokinetic shoulder muscle strength from baseline to 8 weeks
Zeitfenster: Baseline and 8 weeks
|
Isokinetic shoulder muscle strength was assessed using an isokinetic dynamometer during internal and external rotation.
Measurements were performed before and after the 8-week intervention period.
|
Baseline and 8 weeks
|
|
Change in isokinetic shoulder muscle endurance from baseline to 8 weeks
Zeitfenster: Baseline and 8 weeks
|
Isokinetic shoulder muscle endurance was assessed using an isokinetic dynamometer during repeated shoulder internal and external rotation movements.
Measurements were performed before and after the 8-week intervention period.
|
Baseline and 8 weeks
|
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
Schlüsselwörter
Andere Studien-ID-Nummern
- GAZI-2022-933-SS
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
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 .
Klinische Studien zur Übungstherapie
-
Sigmund Freud PrivatUniversitatNoch keine RekrutierungStreicheln | Akuter ischämischer Schlaganfall | Thrombolyse | DAPT (Duale Thrombozytenaggregationshemmer-Therapie) | SAPT (Single Antiplatelet Therapy)Österreich, Deutschland, Schweiz
-
Baylor College of MedicinePatient-Centered Outcomes Research Institute; M.D. Anderson Cancer Center; The... und andere MitarbeiterAbgeschlossenHerzinsuffizienz im Endstadium | Bridge-to-Transplant-LVAD-Platzierung (BTT) | Destination Therapy LVAD-Platzierung (DT) | Ablehnung der LVAD-Platzierung (Ablehner) | LVAD-BetreuerVereinigte Staaten
-
OCEAN-SHD Study GroupRekrutierungAortenstenose | Aspirin | TAVI (Transkatheter-Aortenklappenimplantation) | DAPT (Duale Thrombozytenaggregationshemmer-Therapie) | SAPT (Single Antiplatelet Therapy)Japan
-
Dana-Farber Cancer InstituteAbgeschlossenBrustkrebs | Magen-Darm-Krebs | Oral Cancer Directed Therapy | Orale ChemotherapieVereinigte Staaten
Klinische Studien zur ShoulderSphere-Based Exercise Program
-
National Taiwan University HospitalAbgeschlossenDepression | Herzfehler | Lebensqualität | Gebrechlichkeit | Zuhause zu Walking ExcerciseTaiwan
-
Vanderbilt University Medical CenterAbgeschlossenDepression | Betonen | Ausbrennen | Angst | SelbstmitgefühlVereinigte Staaten
-
Mersin UniversityAbgeschlossenSucht nach sozialen MedienTruthahn
-
The Hong Kong Polytechnic UniversityNoch keine Rekrutierung
-
University of OklahomaThe University of Texas Health Science Center, Houston; National Institute on... und andere MitarbeiterAbgeschlossenSubstanzgebrauchsstörungen | Gesundheitsverhalten | Adhärenz, Patient | Beeinträchtigung der psychischen GesundheitVereinigte Staaten
-
Istanbul Medeniyet UniversityNoch keine RekrutierungDepression | Betonen | Angst | Wohlbefinden, psychologisch
-
Norwegian University of Science and TechnologyOslo University Hospital; Guy's and St Thomas' NHS Foundation Trust; Cedars-Sinai... und andere MitarbeiterAbgeschlossenNeubildungen | KachexieNorwegen, Vereinigtes Königreich, Kanada, Deutschland, Vereinigte Staaten, Schweiz