肩甲骨運動学の回旋腱板修復後の早期肩甲骨筋を強化する運動を強化する有効性
回旋腱板修復後の加速されたリハビリテーションプログラムにおける下部ラッペジウスとserratus前筋の早期強化
The study investigates the effect of accelerate rehabilitation protocol(adding scapular strengthen exercises (lower trapezius and serratus anterior) from week 1) after arthroscopic rotator cuff repair on scapular upward rotation during shoulder elevation.
調査の概要
状態
詳細な説明
The study will consist of two groups, each participating in an accelerated rehabilitation program that will start in the first week after surgery and continue until week 12. However, the groups will follow different protocols.
The first group will follow an accelerated rehabilitation protocol with early strengthening of the scapular stabilizer muscles, specifically the lower trapezius (LT) and serratus anterior (SA). This group will begin gradual active range of motion (ROM) for the glenohumeral (GH) joint from week 4 post-operative until week 12, as well as scapular muscle strengthening exercises starting from the first week.
The second group will follow a protocol with delayed strengthening of the scapular stabilizer muscles. In this group, active ROM for the GH joint and scapular activation exercises (including protraction, retraction, and depression) will begin from week 6 and continue until week 12.
Patients will be required to wear a sling for the first 6 weeks or as recommended by the physician, removing it only during therapy sessions and home exercises.
Outcomes will be measured at three points: at week 3 for baseline assessment, and then reassessed at weeks 6 and 12.
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
-
-
-
Alexandria、エジプト、03
- wengat hospital (El Raml Children hospital)
-
Alexandria、エジプト
- wengat hospital (El Raml Children hospital)
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Patients after arthroscopic rotator cuff repair.
- Both gender between age 30 to 50 years
- Small and medium supraspinatus tear
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：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的：Early strengthening of Scapular stabilizer muscle and GH Active range of motion
Act as study group will receive accelerated protocol with early strengthening of scapular stabilizer muscle of lower trapezius, and serratus anterior and early active GH range of motion (AESA) rehabilitation program. |
adding early scapular strengthening (lower trapezius and serratus anterior) exercise in Rehabilition program after rotator cuff repair surgery |
|
アクティブコンパレータ：Delay strengthening of Scapular stabilizer muscles and GH Active range of motion
Act as control group will receive Accelerated protocol with delay strengthening of scapular stabilizer muscles and GH active range of motion (ADSA) rehabilitation program |
adding early scapular strengthening (lower trapezius and serratus anterior) exercise in Rehabilition program after rotator cuff repair surgery |
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 |
|---|---|---|
|
Upward rotation of the scapula
時間枠：At week 3 and week 9 and week 12 after arthroscopic rotator cuff repair
|
Measuring the degree of upward rotation of the scapula during shoulder elevation using baseline bubble inclinometer |
At week 3 and week 9 and week 12 after arthroscopic rotator cuff repair
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
glenohumeral shoulder elevation
時間枠：At week 3 and week 9 and week 12 after arthroscopic rotator cuff repair
|
Measuring the degree of glenohumeral shoulder flexion, abduction, internal rotion and external rotation using a baseline bubble inclinometer |
At week 3 and week 9 and week 12 after arthroscopic rotator cuff repair
|
|
scapular muscles strength
時間枠：At week 3, week 9 and week 12 after arthroscopic rotator cuff repair
|
measuring the muscle strength for the serratus anterior, lower trapezius, and upper trapezius using the Active Force 2 device dynamometer |
At week 3, week 9 and week 12 after arthroscopic rotator cuff repair
|
協力者と研究者
スポンサー
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
追加の関連 MeSH 用語
その他の研究ID番号
- P.T.REC/012/005178
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。