- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07349355
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
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Selçuk Görücü
- Phone Number: +9005079554505
- Email: selcukgorucu@gmail.com
Study Locations
-
-
-
Aydin, Turkey (Türkiye)
- Adnan Menderes University
-
Contact:
- Selçuk Görücü
- Phone Number: +9005079554505
- Email: selcukgorucu@gmail.com
-
Principal Investigator:
- Selçuk Görücü
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria: Students were included in the study if they were:
- 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
Exclusion Criteria:
- 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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group 1
Group 1 receives training in a simulation laboratory environment using standard patient interventions.
|
Group 1 receives training in a simulation laboratory environment using standard patient interventions.
|
|
Experimental: Group 2
Group 2 receives training in a real hospital setting through on-site simulations and standardized patient interventions.
|
Group 2 receives training in a real hospital setting through on-site simulations and standardized patient interventions.
|
|
No Intervention: Group 3
Group 3 is the control group.
They receive traditional classroom-based theoretical instruction.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Medical error tendency scale scores of final-year nursing students
Time Frame: From registration to week 8 of intervention
|
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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Medical error attitude scale scores of final year nursing students
Time Frame: From registration to week 8 of intervention
|
Medical Error Attitude Scale The total scale score is calculated by dividing the total score by the number of items. The cutoff point is set at 3. Healthcare personnel scoring below 3 on the scale are considered incompetent. |
From registration to week 8 of intervention
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2024/024
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- SAP
- ICF
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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