Patient Education and Sling Use After Shoulder Surgery
Evaluation of Educational Pamphlets and Female Patient Experience With Post-operative Sling-Wear
This study will evaluate whether educational pamphlets can help patients safely manage personal hygiene, household activities, and female-specific self-care while wearing a sling after surgery. The study will also examine whether following sling-use instructions is associated with better short-term recovery and patient-reported outcomes for up to 6 months after surgery.
調査の概要
状態
条件
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究場所
-
-
Pennsylvania
-
Philadelphia、Pennsylvania、アメリカ、19107
- Rothman Orthopaedic Institute
-
-
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:
- Participants scheduled to undergo shoulder surgery at Rothman Orthopaedics that requires more than 1 week of postoperative shoulder sling use.
- Participants who are able to provide informed consent.
- Participants who have sufficient English-language proficiency to understand the study materials and complete the study questionnaires.
Exclusion Criteria:
- Participants undergoing shoulder surgery that does not require more than 1 week of postoperative shoulder sling use.
- Participants who do not have sufficient English-language proficiency to understand the study materials and complete the study questionnaires.
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 |
|---|---|
|
アクティブコンパレータ：Control Group - Standard postoperative education
Standard postoperative education |
Participants will receive the standard postoperative education and instructions provided by their treating orthopedic physician for patients undergoing shoulder surgery requiring postoperative sling use. |
|
アクティブコンパレータ：Pamphlet Intervention Group
Standard postoperative education + "Living with a Sling" educational pamphlets |
Participants will receive standard postoperative education plus educational pamphlets providing guidance on performing daily activities while wearing a shoulder sling. The pamphlets address personal hygiene, household tasks, and self-care. Female participants will also receive a pamphlet addressing female-specific self-care. |
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 |
|---|---|---|
|
Sling adherence
時間枠：4 to 6 weeks after surgery
|
Sling adherence will be assessed using patient-reported survey responses regarding adherence to prescribed shoulder sling use during the postoperative period. |
4 to 6 weeks after surgery
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Patient-reported shoulder function
時間枠：6 months after surgery
|
Shoulder function will be assessed using the American Shoulder and Elbow Surgeons (ASES) score. |
6 months after surgery
|
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Patient-reported shoulder status
時間枠：6 months after surgery
|
Patient-reported shoulder status will be assessed using the Single Assessment Numeric Evaluation (SANE). |
6 months after surgery
|
|
Patient experience while wearing a shoulder sling
時間枠：6 weeks after surgery
|
Participants will complete a questionnaire assessing their experience performing daily activities, including personal hygiene, household tasks, and self-care while wearing a shoulder sling. |
6 weeks after surgery
|
|
Preparedness for postoperative activities
時間枠：6 weeks after surgery
|
Participants will report their preparedness and ability to manage daily activities while wearing a shoulder sling. |
6 weeks after surgery
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
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
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。