Simulation-Based Interprofessional Education for Operating Room Teams

Официальное название

Simulation-Based Interprofessional Education for Surgical Residents: A Prospective Study Design for Team-Based Competency Development

Обзор

This single-center, prospective, single-arm pilot study will evaluate a simulation-based interprofessional education program for early-career operating room team members at Yongin Severance Hospital. Participants will include postgraduate year 1-2 surgical residents, newly appointed anesthesia nurse practitioners, and newly appointed operating room nurses. Participants will complete two simulation-based interprofessional education sessions, each including scenario-based team training and structured debriefing. Teamwork self-efficacy and readiness for interprofessional learning will be assessed before and after the educational intervention. The study will also assess program completion as a feasibility outcome. Optional semi-structured interviews may be conducted to explore participants' perceptions of the program and suggestions for improvement.

Подробное описание

Effective teamwork and communication among operating room team members are important for patient safety and perioperative care. However, early-career surgical residents and nursing staff may have limited opportunities to learn team-based competencies together in a structured, interprofessional format. This study is a single-center, prospective, single-arm pilot study designed to evaluate the feasibility and preliminary educational effects of a simulation-based interprofessional education program for operating room teams. Eligible participants will be assigned to interprofessional teams consisting of surgical residents, anesthesia nurse practitioners, and operating room nurses. The educational intervention will include two simulation-based sessions conducted during the study period. Each session will last approximately 60 minutes and will include a scenario-based team exercise followed by structured debriefing. Representative scenario themes may include operating room safety events, communication challenges, equipment or instrument-related events, and intraoperative crisis management. The primary outcome is the change in teamwork self-efficacy from baseline to Week 7, assessed using a 15-item interprofessional teamwork self-efficacy questionnaire. Secondary outcomes include the change in readiness for interprofessional learning, assessed using the Readiness for Interprofessional Learning Scale, and program completion rate. Optional semi-structured interviews may be conducted after completion of the educational sessions to explore participants' perceptions of the program, perceived relevance to clinical practice, and suggestions for improvement.

Interview participation and audio recording, if performed, will be optional and based on separate consent. No investigational drug, biologic product, or medical device will be used in this study.

Вмешательства

• Поведенческое Simulation-Based Interprofessional Education
  The intervention consists of two 60-minute simulationbased interprofessional education sessions for operating room team members. Each session includes a representative operating room scenario and structured debriefing. Debriefing topics include role clarity, shared mental model, situational awareness, open communication, cross-monitoring, mutual respect, and application to clinical practice.

Первичные конечные точки

• Change in teamwork selfefficacy score [Срок оценки: Baseline and Week 7]

Вторичные конечные точки (2)

• Change in readiness for interprofessional learning score [Срок оценки: Baseline and Week 7]
• Program completion rate [Срок оценки: Through Week 7]

Критерии участия

Критерии включения

• Adults aged 19 years or older.
• Affiliated with Yongin Severance Hospital and meeting one of the following criteria:
• Postgraduate year 1-2 surgical resident;
• Newly appointed anesthesia nurse practitioner with less than 6 months of experience in the relevant role;
• Newly appointed operating room nurse with less than 6 months of operating room experience.
• Able to participate in the planned study procedures during the study period.
• Able and willing to provide written informed consent.

Критерии исключения

• Individuals who do not provide written informed consent.
• Individuals who are unable to complete the baseline or post-intervention questionnaires.
• Individuals whose rotation, leave of absence, resignation, transfer, or work schedule change makes participation in the study procedures infeasible.
• Individuals judged by the investigator to be inappropriate for study participation.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Организация здравоохранения

Центры проведения

South Korea · 1 центр

• Yonsei University Yongin Severance Hospital — Yongin-si

Идентификаторы

NCT: NCT07570134 · Surgical-IPE-001 · 6-2025-0077

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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