Transfer of Non-technical Skills From Simulation to Clinical Practice
Are the Non Technical Skills Taught to Residents in Anesthesiology During in Situ Simulation Sessions Transferred to Clinical Practice
Since 1988, simulation has been proposed as a teaching tool in Anesthesia. The simulation environment allows to teach learners non-technical skills which are a combination of cognitive, social, and personal resources complementary to procedural skills that contribute to an efficient and safe performance.
Non-technical skills traditionally used in Anesthesia are task management, situational awareness, teamwork and decision making. They can be indirectly measured with validated scales (e.g. Anesthesia Non-Technical Skills (ANTS) system). In addition to these basic skills, specific skills such as Anesthesia Crisis Resource Management (ACRM) are required when the patient presents a critical clinical situation.
Simulation, as proposed by Gaba, was initially practiced in centers specifically designed for this purpose. More recently, we have proposed the model of in situ simulation, i.e. in the usual workplace with the usual work team, as another option for the practice of simulation.
There are many theories about the transfer of learning. Transfer can be defined as what remains of the completed training that the learner actually uses, i.e. the final real effect.
Nevertheless, almost 30 years after the introduction of simulation in the training of anesthesiologists, data demonstrating the interest of this teaching in terms of transfer of learning of non-technical skills to clinical practice or benefits for patients are rare.
The main objective of this study is to evaluate the transfer of non-technical skills taught in a training program including in situ simulation to clinical practice by anesthesiology residents.
調査の概要
研究の種類
入学 (予想される)
段階
- 適用できない
連絡先と場所
研究場所
-
-
-
Liège、ベルギー、4000
- CHU de Liège - Sart-Tilman
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-
参加基準
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
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:
- Internship in the ambulatory surgery unit
Exclusion Criteria:
- Refusal to participate
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:他の
- 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 |
|---|---|
|
介入なし:Control group
Anesthesiology residents do not receive any in situ simulation sessions during the observation period
|
|
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実験的:Simulation group
Anesthesiology residents receive in situ simulations sessions during the observation period
|
2 sessions of in situ simulation with 4 crisis scenarios and debriefing focused on non technical skills
|
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 |
|---|---|---|
|
ANTS (Anesthesia non technical skills) score
時間枠:Once a day for 5 consecutive days between the first and the 15th day after enrollment in the study
|
15 items - From 1(poor) to 4 (good) for each item - Minimum 15 - Maximum 60
|
Once a day for 5 consecutive days between the first and the 15th day after enrollment in the study
|
|
ANTS (Anesthesia non technical skills) score
時間枠:Once a day for 5 consecutive days between the 30th and 45th day after enrollment
|
15 items - From 1(poor) to 4 (good) for each item - Minimum 15 - Maximum 60
|
Once a day for 5 consecutive days between the 30th and 45th day after enrollment
|
|
ANTS (Anesthesia non technical skills) score
時間枠:Once a day for 5 consecutive days between the 3rd and the 4th month after enrollment
|
15 items - From 1(poor) to 4 (good) for each item - Minimum 15 - Maximum 60
|
Once a day for 5 consecutive days between the 3rd and the 4th month after enrollment
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
DOPS (Direct Observation of Procedural Skills) scale
時間枠:Once within the first 15 days of enrollment
|
Once within the first 15 days of enrollment
|
|
DOPS (Direct Observation of Procedural Skills) scale
時間枠:Once between the 30th and the 45th day after enrollment
|
Once between the 30th and the 45th day after enrollment
|
|
DOPS (Direct Observation of Procedural Skills) scale
時間枠:Once between the 3rd and the 4th month after enrollment
|
Once between the 3rd and the 4th month after enrollment
|
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 (予想される)
研究の完了 (予想される)
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
- 2018-71
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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