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.
調査の概要
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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Istanbul
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Istanbul、Istanbul、トルコ（Türkiye）、34815
- Istanbul Medipol University
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：処理
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的：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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アクティブコンパレータ：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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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Occupational performance and satisfaction measured by the Canadian Occupational Performance Measure (COPM)
時間枠：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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協力者と研究者
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- E-10840098-202.3.02-8555
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。