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Clinical Trials in China / NCT07527429
Active, not recruiting Not applicable

Procedure Manual-Based Simulation Training to Improve Operating Room Nurses' Core Competencies

NCT07527429 · tracked via the Priya Life Science China tracker
Sponsor
Hiroshima University
Phase
Not applicable
Started
2026-04-20
Last updated
2026-07-08

Condition(s) studied

Core CompetencyPatient SafetyInterprofessional CollaborationSurgical OutcomeJob Satisfaction

Investigational drug(s) / intervention(s)

Procedure Manual-Based Simulation Training

Procedure Manual-Based Simulation Training: The intervention consists of a simulation training program of procedure manuals focused on two surgical procedures: Total Hip Replacement (THR) and Retrograde Intrarenal Surgery (RIRS). Training Phase (2 weeks): Participants attend two sessions (one per procedure). Each session includes a 1-hour lecture and 2 hours of hands-on simulation practice. Self-Study: Participants are provided with a digital E-manual for continuous review. Implementation Phase (6 weeks): Participants apply the standardized procedure manuals in real surgical settings with follow-up support from the research team.

Study summary

This study aims to evaluate the effectiveness of a procedure manual-based simulation training program in improving the core competencies of operating room nurses in a Cambodian national hospital. Operating room nurses play a critical role in maintaining patient safety, assisting the surgical team, and ensuring efficient surgical workflow.

This study will use a single-group quasi-experimental pre-post design. Baseline data will be collected before the intervention to assess operating room nurses' core competencies, interprofessional collaboration, job satisfaction, and surgical procedure duration.

Participants will receive structured educational sessions and simulation-based training based on standardized surgical procedure manuals. After the training phase, nurses will implement the procedure manuals during real surgical procedures for six weeks. End-line data will be collected to evaluate improvements in competency levels, teamwork, job satisfaction, and surgical efficiency.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
Accepted
Inclusion Criteria: * Registered nurses who are appointed to work in the intraoperative phase of Cambodia-China Friendship Preah Kossamak Hospital. * Registered nurses at Cambodia-China Friendship Preah Kossamak Hospital who are willing to participate in the study. Exclusion Criteria: * Registered Nurses Cambodia-China Friendship Preah Kossamak Hospital who are unable to participate in intervention requirements. * Registered Nurses Cambodia-China Friendship Preah Kossamak Hospital who are scheduled to participate in hospital mission assignments.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Cambodia-China Friendship Preah Kossamak Hospital Phnom Penh Phnom Penh
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07527429 on ClinicalTrials.gov ↗ ← All trials in China