NCT07570134

Brief Summary

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.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
12mo left

Started May 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress2%
May 2026Apr 2027

First Submitted

Initial submission to the registry

April 29, 2026

Completed
2 days until next milestone

Study Start

First participant enrolled

May 1, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

May 6, 2026

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2027

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 25, 2027

Last Updated

May 6, 2026

Status Verified

April 1, 2026

Enrollment Period

10 months

First QC Date

April 29, 2026

Last Update Submit

April 29, 2026

Conditions

Keywords

Interprofessional educationsimulation trainingoperating roomteamworksurgical educationnursing educationpatient safetyreadiness for interprofessional learningRIPLS

Outcome Measures

Primary Outcomes (1)

  • Change in teamwork selfefficacy score

    Teamwork self-efficacy will be assessed using a 15-item interprofessional teamwork selfefficacy questionnaire. Each item is scored on a 6-point Likert-type scale, with higher scores indicating greater confidence in team-based competencies. The outcome will be calculated as the change in total score from baseline to Week 7.

    Baseline and Week 7

Secondary Outcomes (2)

  • Change in readiness for interprofessional learning score

    Baseline and Week 7

  • Program completion rate

    Through Week 7

Study Arms (1)

Simulation-Based Interprofessional Education

EXPERIMENTAL

Participants assigned to this single study arm will receive two simulation-based interprofessional education sessions during the study period. Each session will include a scenario-based operating room team exercise and structured debriefing focused on teamwork, role clarity, communication, situational awareness, and collaboration.

Behavioral: Simulation-Based Interprofessional Education

Interventions

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.

Simulation-Based Interprofessional Education

Eligibility Criteria

Age19 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Yonsei University Yongin Severance Hospital

Yongin-si, Gyeonggi-do, 16995, South Korea

Location

Study Officials

  • Jeehye Lee, MD

    Yonsei University Yongin Severance Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
SINGLE GROUP
Model Details: All participants will receive the same simulation-based interprofessional education intervention and will be evaluated using a pre-post design.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Assistant Professor

Study Record Dates

First Submitted

April 29, 2026

First Posted

May 6, 2026

Study Start

May 1, 2026

Primary Completion (Estimated)

February 28, 2027

Study Completion (Estimated)

April 25, 2027

Last Updated

May 6, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared because this is a small, single-center educational study involving occupational groups that may be indirectly identifiable even after de-identification. Aggregate results may be shared through presentations or publications without identifying individual participants.

Locations