Peer-Learning Versus Physician-Led POCUS Training for Nurse Practitioners in Integrative Volume Status Assessment
Feasibility of a Peer-Learning Ultrasound Program to Enhance Nurse Practitioners' Competence in Integrative Volume Status Assessment
調査の概要
状態
詳細な説明
This quasi-experimental study aims to compare two instructional models-physician-led versus peer NP-led POCUS training-and their effects on learners' outcomes and clinical skill performance.
Methods:
Sixty NPs, either in practice or under training, will be recruited and non-randomly assigned to either the experimental group (peer-led instruction) or the control group (physician-led instruction), based on their course availability, simulating real-world clinical education allocation:
- Experimental group: Hands-on training led by NPs who have completed a structured POCUS curriculum and passed both teaching and practical assessments.
- Control group: Hands-on training delivered by specialist physicians.
To ensure the quality and standardization of instructional delivery and operational procedures, two groups of nurse practitioners received the training program in separate cohorts. The educational intervention was structured into two phases: the first phase consisted of a two-hour online course covering fundamental ultrasound theory, relevant anatomical structures, and key points in clinical application; the second phase was a four-hour in-person hands-on workshop focusing on clinical scanning techniques and image interpretation skills. The instructional content encompassed five core structures: (1) inferior vena cava (IVC) assessment, (2) pleural effusion detection, (3) ascites identification, (4) hydronephrosis evaluation, and (5) bladder volume estimation and urinary retention interpretation.
Participants completed a pre-test prior to the training, a first post-test immediately after the course, and a second post-test three months later. The assessment tools included: (1) a POCUS knowledge questionnaire, (2) a self-confidence scale, (3) an image interpretation assessment, and (4) an Objective Structured Clinical Examination (OSCE).
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：Chiang-Yi Chen, master
- 電話番号：+886928124530
- メール：a865292@gmail.com
研究場所
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Taipei
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Taipei、Taipei、台湾、100
- National Taiwan University Hospital
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コンタクト：
- Chiang-Yi Chen, master
- 電話番号：0928124530
- メール：a865292@gmail.com
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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:
Participants aged 18 years or older. Licensed nurse practitioners or nurse practitioner trainees currently enrolled in an accredited nurse practitioner training program.
Able to understand the study procedures and provide written informed consent. Able to participate in the complete training program and study assessments, including baseline, post-training, and 1-month follow-up assessments.
No prior formal POCUS training, or only limited basic exposure without systematic training experience.
Exclusion Criteria:
Participants who have previously completed a formal point-of-care ultrasound training program.
Participants who are unable to complete the full training program or study assessment procedures.
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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 |
|---|---|
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実験的：Nurse Practitioner-Led Peer Teaching Group
Participants in this arm will receive a structured POCUS training program delivered by trained nurse practitioner instructors.
The intervention includes a 2-hour online course covering basic ultrasound principles, relevant anatomy, and clinical applications, followed by a 4-hour hands-on practice session focused on integrative volume status assessment, including IVC, pleural effusion, ascites, hydronephrosis, and bladder assessment.
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Participants will receive a structured point-of-care ultrasound training program delivered by trained nurse practitioner instructors.
The program includes a 2-hour online lecture and a 4-hour hands-on practice session.
Training focuses on integrative volume status assessment, including ultrasound evaluation of the inferior vena cava, pleural effusion, ascites, hydronephrosis, and bladder volume or urinary retention.
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アクティブコンパレータ：Experimental
Participants in this group will receive the same structured POCUS training program delivered by trained physician instructors.
The program includes a 2-hour online lecture and a 4-hour hands-on practice session focused on integrative volume status assessment, including inferior vena cava, pleural effusion, ascites, hydronephrosis, and bladder assessment.
|
Participants will receive a structured point-of-care ultrasound training program delivered by trained nurse practitioner instructors.
The program includes a 2-hour online lecture and a 4-hour hands-on practice session.
Training focuses on integrative volume status assessment, including ultrasound evaluation of the inferior vena cava, pleural effusion, ascites, hydronephrosis, and bladder volume or urinary retention.
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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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Change in POCUS Clinical Performance Score
時間枠：Baseline, immediately after the training program, and 1 month after the training program
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POCUS clinical performance will be assessed using an Objective Structured Clinical Examination (OSCE).
Participants will be evaluated on ultrasound probe positioning, image acquisition, anatomical identification, clinical interpretation, and integration of findings for volume status assessment, including inferior vena cava, pleural effusion, ascites, hydronephrosis, and bladder assessment.
Higher scores indicate better clinical performance.
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Baseline, immediately after the training program, and 1 month after the training program
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Change in POCUS Knowledge Score
時間枠：Baseline, immediately after the training program, and 1 month after the training program
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POCUS knowledge will be assessed using a structured 10-item questionnaire covering basic ultrasound principles, organ identification, and clinical applications.
Higher scores indicate better POCUS knowledge.
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Baseline, immediately after the training program, and 1 month after the training program
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協力者と研究者
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
キーワード
その他の研究ID番号
- 202507102RINE
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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