Operating Room Orientation Video Education in Patients Undergoing Prostate Surgery
The Effect of Operating Room Orientation Video Education Applied at Different Times on Postoperative Pain and Anxiety in Patients Undergoing Prostate Surgery
調査の概要
状態
条件
詳細な説明
The study will evaluate whether the timing of operating room orientation video education influences postoperative pain and state anxiety in patients undergoing surgery for benign prostatic hyperplasia. The intervention consists of a 5-minute video designed to familiarize patients with the perioperative environment and expected procedures. The video includes information about the operating room environment, the operating table, patient positioning, information related to the surgical process, the post-anesthesia care unit, and patient transfer.
Participants will be randomly allocated in a 1:1:1 ratio to one of three parallel groups. Participants in the first intervention group will receive the video approximately one day before surgery in the surgical ward. Participants in the second intervention group will receive the same video approximately 30 minutes before surgery in the operating room waiting unit. Participants in the control group will receive routine preoperative information according to standard clinical practice.
Pain intensity will be assessed using the Visual Analog Scale, and state anxiety will be assessed using the State-Trait Anxiety Inventory-State Anxiety Scale. Assessments will be performed one day before surgery, before the intervention in the operating room waiting unit, and six hours after surgery in the surgical ward.
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前：Beyza Çakır
- 電話番号：+905372600955
- メール：beyzacakir7856@gmail.com
研究場所
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Atakum
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Samsun、Atakum、トルコ（Türkiye）、55500
- Ondokuz Mayıs University Health Practice and Research Center
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コンタクト：
- Beyza Çakır
- 電話番号：+905372600955
- メール：beyzacakir7856@gmail.com
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主任研究者：
- Beyza Çakır
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副調査官：
- Özge İşeri, Associate professor
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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:
- Being conscious and able to communicate. Being able to read and understand Turkish. Voluntarily agreeing to participate in the study and providing informed consent.
Having no visual or hearing impairment that would interfere with viewing the educational video or completing the study assessments.
Undergoing prostate surgery for the first time. Being 18 years of age or older.
Exclusion Criteria:
- Having a diagnosed psychiatric disorder. Having a chronic pain syndrome. Being scheduled for emergency surgery. Having previously received similar operating room orientation education.
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：支持療法
- 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：Ward Video Education Group
Participants will receive a 5-minute operating room orientation video approximately one day before surgery in the surgical ward.
|
A 5-minute video-based educational intervention designed to familiarize patients with the operating room environment and the perioperative process.
The video includes information about the operating room environment, operating table, patient positioning, information related to the surgical process, the post-anesthesia care unit, and patient transfer.
|
|
実験的：Operating Room Waiting Unit Video Education Group
Participants will receive the same 5-minute operating room orientation video approximately 30 minutes before surgery in the operating room waiting unit.
|
A 5-minute video-based educational intervention designed to familiarize patients with the operating room environment and the perioperative process.
The video includes information about the operating room environment, operating table, patient positioning, information related to the surgical process, the post-anesthesia care unit, and patient transfer.
|
|
アクティブコンパレータ：Routine Information Control Group
Participants will receive routine preoperative information according to standard clinical practice without the study-specific operating room orientation video.
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Participants will receive routine preoperative information according to standard clinical practice without the study-specific operating room orientation video.
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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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Postoperative state anxiety
時間枠：From baseline to 6 hours after surgery
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State anxiety will be assessed using the State-Trait Anxiety Inventory-State Anxiety Scale (STAI-S), using the Turkish adaptation by Necla Öner and Ayhan Le Compte.
State anxiety will be assessed one day before surgery in the surgical ward, before video education in the operating room waiting unit, and 6 hours after surgery in the surgical ward.
The primary postoperative assessment will be the STAI-S score at 6 hours after surgery.
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From baseline to 6 hours after surgery
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Postoperative pain intensity
時間枠：From baseline to 6 hours after surgery
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Pain intensity will be assessed using the Visual Analog Scale (VAS).
Pain will be assessed one day before surgery in the surgical ward, before video education in the operating room waiting unit, and 6 hours after surgery in the surgical ward.
The primary postoperative assessment will be the VAS score at 6 hours after surgery.
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From baseline to 6 hours after surgery
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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 (推定)
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
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
- 2025/1127
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?
IPD プランの説明
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
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