Simulation Practices and Medical Error Tendencies in Nursing Students
The Effect of In-Situ Simulation and Standardized Patient Practice on Medical Error Tendencies and Attitudes of Senior Nursing Students
1 other identifier
interventional
81
1 country
1
Brief Summary
As the professional group that has the most frequent contact with patients, nurses are critical to the sustainability of safe care. Literature demonstrates that nursing practice is prone to error due to heavy workloads, time pressures, complex clinical tasks, inadequate rest, inappropriate working conditions, and the physiological strain of demanding shifts. When these conditions strain both physical and cognitive resources, the risk of errors during treatment administration increases. Medical errors remain one of the most devastating realities of healthcare. Data from the World Health Organization reveals the significant morbidity and mortality caused by errors on a global scale. Numerous studies have demonstrated that student nurses have a significant rate of errors, and those with limited clinical experience are particularly at risk in fundamental areas such as medication administration, asepsis, and patient identification. Increasing patient numbers, short stays, rapid turnover, and the intense pace of clinics negatively impact student nurses' ability to provide safe care, prompting both educators and students to seek stronger pedagogical solutions. This is where simulation-based training comes into play. Simulation is emerging as a contemporary teaching approach that enables students to develop their clinical skills, communication, decision-making, and self-efficacy in a risk-free, safe, and structured environment. It is increasingly being used because it supports knowledge and skill transfer, reduces fear and anxiety, strengthens self-confidence, and provides the opportunity to experience errors. In-situ simulation and standardized patient practice offer strong potential for reducing students' error proneness by providing an experience closest to real-world clinical situations. However, the lack of a study in the literature examining the effects of these two methods, particularly on the medical error proneness and attitudes of final-year nursing students, is a significant gap. This study aims to strengthen a critical area of nursing education. The aim is to evaluate the impact of in-situ simulation and standardized patient practice on final-year nursing students' medical error proneness and attitudes toward medical errors and to reveal how they transform students' competencies in providing safe care.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 24, 2025
CompletedStudy Start
First participant enrolled
January 15, 2026
CompletedFirst Posted
Study publicly available on registry
January 16, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedJanuary 16, 2026
January 1, 2026
2 months
November 24, 2025
January 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Medical error tendency scale scores of final-year nursing students
Medical Error Tendency Scale The minimum possible score is 1, and the maximum is 5. While the scale does not have a cutoff point, an increase in the mean score indicates a low tendency for the nurse to make medical errors, while a decrease in the mean score indicates a high tendency to make errors.
From registration to week 8 of intervention
Secondary Outcomes (1)
Medical error attitude scale scores of final year nursing students
From registration to week 8 of intervention
Study Arms (3)
Group 1
EXPERIMENTALGroup 1 receives training in a simulation laboratory environment using standard patient interventions.
Group 2
EXPERIMENTALGroup 2 receives training in a real hospital setting through on-site simulations and standardized patient interventions.
Group 3
NO INTERVENTIONGroup 3 is the control group. They receive traditional classroom-based theoretical instruction.
Interventions
Group 1 receives training in a simulation laboratory environment using standard patient interventions.
Group 2 receives training in a real hospital setting through on-site simulations and standardized patient interventions.
Eligibility Criteria
You may qualify if:
- A senior nursing student at Aydın Adnan Menderes University Faculty of Nursing
- Volunteering to participate in the study
- Not absent at any time during the study period
- Working/not working as a nurse
You may not qualify if:
- Graduated from a health vocational high school
- Admitted through the Foreign Student Exam (YÖS)
- Graduated from a health-related associate's degree program and then enrolled in the nursing department through the Vertical Transfer Exam (DGS)
- Students who did not wish to participate in the study were excluded from the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Selçuk Görücülead
Study Sites (1)
Adnan Menderes University
Aydin, Turkey (Türkiye)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Lecturer
Study Record Dates
First Submitted
November 24, 2025
First Posted
January 16, 2026
Study Start
January 15, 2026
Primary Completion
March 15, 2026
Study Completion
May 1, 2026
Last Updated
January 16, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- SAP, ICF, CSR
- Time Frame
- August 2026-December 2026
- Access Criteria
- Access to data will be available only after a written request from the researcher and a review by the research team for scientific relevance. Access will only be provided by securely transmitting designated datasets via email; no sharing will be made via any open-access repository or online platform.
This study does not plan to share raw data at the individual level. However, to promote transparency of research findings, summary data (demographic characteristics, pretest and posttest scores, group comparisons, and analysis results) that do not include participant identification will be shared with researchers upon request. No personal identifying information (name, contact information, institutional information, etc.) will be shared.