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Die klinische Studie NCT06618443 für Shoulder Adhesive Capsulitis ist noch nicht rekrutierend. In der Kartenansicht des Klinische Studien Radar und den KI-Entdeckungstools finden Sie alle Details. Oder stellen Sie hier Ihre Fragen. | ||
Eine Studie entspricht den Filterkriterien
Kartenansicht
Scapular Mobilization With Arm Movement in Patients With Adhesive Capsulitis. 50
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Die klinische Studie NCT06618443 ist eine interventionsstudie zur Untersuchung von Shoulder Adhesive Capsulitis und hat den Status noch nicht rekrutierend. Der Start ist für 15. Oktober 2024 geplant, bis 50 Teilnehmer aufgenommen werden. Durchgeführt von Beni-Suef-Universität wird der Abschluss für 15. Februar 2025 erwartet. Die Daten von ClinicalTrials.gov wurden zuletzt am 1. Oktober 2024 aktualisiert.
Kurzbeschreibung
50 patients with shoulder adhesive capsulitis were admitted. the patients will receive scapular mobilization (downward or upward mobilization) associated with arm movements. The percentage of improvement in shoulder ROM of flexion, abduction, and external rotation; and decrease in shoulder pain and disability index (SPADI).
Offizieller Titel
Effect of Scapular Mobilization With Arm Movement on Shoulder Pain and Range of Motion and Disability in Older Adults With Adhesive Capsulitis.
Erkrankungen
Shoulder Adhesive CapsulitisWeitere Studien-IDs
- BNS
NCT-Nummer
Studienbeginn (tatsächlich)
2024-10-15
Zuletzt aktualisiert
2024-10-01
Studienende (vorauss.)
2025-02-15
Geplante Rekrutierung
50
Studientyp
Interventionsstudie
PHASE
Nicht zutreffend
Status
Noch nicht rekrutierend
Stichwörter
scapular mobilization; arm movement; pain; range of motion; disability; older adults; adhesive capsulitis
Primäres Ziel
Behandlung
Zuteilungsmethode
Randomisiert
Interventionsmodell
Parallel
Verblindung
Vierfach verblindet
Studienarme/Interventionen
| Teilnehmergruppe/Studienarm | Intervention/Behandlung |
|---|---|
ExperimentellScapular mobilization with movement The treatment consisted of scapular mobilization with arm movement in all directions for 15 min/session for 3 sessions/week for 4 weeks. Scapular mobilization included scapular upward glide and downward glid. Scapular upward glide was performed with shoulder adduction and extension, while scapular downward glide was performed with shoulder abduction and flexion. | Scapular mobilization with movement The treatment consisted of scapular mobilization with arm movement in all directions for 15 min/session for 3 sessions/week for 4 weeks. Scapular mobilization included scapular upward glide and downward glid. Scapular upward glide was performed with shoulder adduction and extension, while scapular downward glide was performed with shoulder abduction and flexion. |
Keine InterventionControl | Nicht zutreffend |
Hauptergebnismessungen
| Ergebnismessung | Beschreibung der Messung | Zeitrahmen |
|---|---|---|
Shoulder Pain and Disability Index (SPADI) | The patient was asked to refer to the degree of their shoulder problems in the previous week by choosing a number on a scale from 0 (no pain or disability) to 10 (extreme pain and disability) for each question 13. The chosen number from each subscale was summed up and transformed into an out-of-100 score. The mean two scales were assigned a sum score out of 100. The higher the end score, the more shoulder pain, or disability. | 3 months |
Shoulder range of motion of flexion, abduction, and external rotation | For evaluating shoulder flexion and abduction, the goniometer was positioned on the distal arm. The patient sat in a vertical position on an elevated-backed chair. To restrain trunk unwanted motion, a belt was put around the patient\'s waist and chair. The patient was directed to lift the tested arm voluntarily with his palm facing the floor.
For evaluating shoulder external rotation, the goniometer was positioned on the proximal forearm next to the wrist joint. The patient was asked to lie supine with flexed hips and knees 45 degrees. The tested arm was placed on the plinth with 90 degrees in shoulder abduction, 90 degrees in elbow flexed, and 0 degrees in wrist joint11. The patient was asked to turn the forearm up to externally rotate the arm. | 3 months |
Scapular dyskinesis | this test was conducted with grasping dumbbells following the bodyweight, 1.4 kg (3 lb) for patients with a weight of lower than 68.1 kg (150 lb), and 2.3 kg (5 lb) for patients with a weight of 68.1 kg or higher. If any patient was unable to carry these predetermined weights, the weight was decreased by 0.5 kg29. Then, the patient was instructed to instantaneously raise his arms overhead with thumbs-up as much as possible at a 3-second count and then lower the arms back to the same starting position at a 3-second count.
This study used a caliper to develop an objective method to measure improved scapular dyskinesis. The height difference between the 2 scapulae was measured with a caliper to the nearest millimeters at the end of the available shoulder ROM. The height difference between the 2 scapulae was defined as the difference between the vertical positions of the 2 inferior angles of the 2 scapulae30. A distance of more than 75 mm between the 2 scapulae was c | 3 months |
Electromyography | Electromyographical analysis of Upper and Lower trapezius and Serratus anterior | 3 months |
Teilnahme-Assistent
Eignungskriterien
Zugelassene Altersgruppen
Ältere Erwachsene
Mindestalter
65 Years
Zugelassene Geschlechter
Alle
- The existence of unilateral adhesive capsulitis (stage II) with incapability of the participant to raise the arm more than 100 degrees in the plane of the scapula
- The presence of any shoulder problem contraindicated for performing exercises to the shoulder joint, such as active inflammatory disease, cancer, active infection, recent subluxations or dislocations, fractures, and surgeries near the shoulder region.
Verantwortliche Partei
Ayman Mohamed, Hauptprüfer, Associate Professor, Beni-Suef University
Zentrale Studienkontakte
Kontakt: Ayman AM Mohamed, PhD, MPT, DPT, +201141776364, [email protected]
Keine Standortdaten vorhanden