TASK-ORIENTED REHABILITATION AFTER ROTATOR CUFF SURGERY
THE EFFECT OF TASK-ORIENTED OCCUPATIONAL THERAPY INTERVENTION ON ACTIVITY PARTICIPATION AFTER ROTATOR CUFF SURGERY: PRE- AND POST-INTERVENTION EVALUATION
Rotator cuff tears negatively affect shoulder stability, range of motion, and performance in daily activities. Postoperative rehabilitation is essential for improving functional recovery and quality of life; however, conventional approaches may not directly target meaningful activity performance.
Task-oriented occupational therapy is a client-centered approach focusing on meaningful and goal-directed activities to enhance functional independence. This randomized controlled trial aims to investigate the effect of task-oriented occupational therapy on activity participation, occupational performance, satisfaction, and functional recovery after rotator cuff surgery.
A total of 30 participants will be randomly assigned to either a task-oriented occupational therapy group or a conventional rehabilitation group. The intervention will be conducted twice weekly for 10 weeks, with 40-minute sessions based on individually prioritized activities identified using the Canadian Occupational Performance Measure. Outcomes will include occupational performance and satisfaction, goal attainment, shoulder function, quality of life, and patient satisfaction.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Istanbul
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Istanbul, Istanbul, Turquie (Türkiye), 34815
- Istanbul Medipol University
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Individuals aged 18 years and older
- Individuals who have undergone rotator cuff surgery
- Medically stable and cleared for participation in a rehabilitation program
- Ability to understand and follow instructions
- Voluntary agreement to participate in the study
Exclusion Criteria:
- - Presence of severe neurological disorders affecting upper extremity function
- Severe cognitive impairment limiting participation
- Additional musculoskeletal conditions affecting the upper extremity
- Postoperative complications that may interfere with rehabilitation
- Participation in another rehabilitation program during the study period
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Task-oriented intervention group
In this group patient who have undergone rototor cuff surgery will receive a task oriented exercise program based on activities off daily living conducted twice a week for ten weeks.
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In this intervention, following rotator cuff surgery, task-oriented occupational therapy sessions based on activities of daily living will be applied.
These sessions will be conducted twice a week for 10 weeks and aim to achieve improvements in participants' activity performance and activity satisfaction.
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Comparateur actif: Conventional rehabilitation group
Participants included in the conventional intervention group will continue with the standard rehabilitation program applied in the postoperative period.
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This intervention includes exercises aimed at improving joint range of motion, enhancing muscle strength, and supporting muscle flexibility.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Occupational performance and satisfaction measured by the Canadian Occupational Performance Measure (COPM)
Délai: Baseline and after 10 weeks of intervention
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Occupational performance and satisfaction will be assessed using the Canadian Occupational Performance Measure (COPM).
The change in COPM performance and satisfaction scores from baseline to post-intervention will be evaluated.
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Baseline and after 10 weeks of intervention
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Collaborateurs et enquêteurs
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Collaborateurs
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- E-10840098-202.3.02-8555
Plan pour les données individuelles des participants (IPD)
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Informations sur les médicaments et les dispositifs, documents d'étude
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