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.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
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Istanbul
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Istanbul, Istanbul, Türkei (türkiye), 34815
- Istanbul Medipol University
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: 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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Aktiver Komparator: 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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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Occupational performance and satisfaction measured by the Canadian Occupational Performance Measure (COPM)
Zeitfenster: 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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Mitarbeiter und Ermittler
Sponsor
Publikationen und hilfreiche Links
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
Andere Studien-ID-Nummern
- E-10840098-202.3.02-8555
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