NCT07349355

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

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
81

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2026

Shorter than P25 for not_applicable

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 24, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

January 15, 2026

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 16, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 15, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2026

Completed
Last Updated

January 16, 2026

Status Verified

January 1, 2026

Enrollment Period

2 months

First QC Date

November 24, 2025

Last Update Submit

January 11, 2026

Conditions

Keywords

In-situ simulationstandardized patientnursing studentsrandomized controlled trialnursing educationmedical error

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

EXPERIMENTAL

Group 1 receives training in a simulation laboratory environment using standard patient interventions.

Other: Standardized patient

Group 2

EXPERIMENTAL

Group 2 receives training in a real hospital setting through on-site simulations and standardized patient interventions.

Other: İn-situ simulation

Group 3

NO INTERVENTION

Group 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 1

Group 2 receives training in a real hospital setting through on-site simulations and standardized patient interventions.

Group 2

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

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

Study Sites (1)

Adnan Menderes University

Aydin, Turkey (Türkiye)

Location

Central Study Contacts

Selçuk Görücü

CONTACT

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

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.

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.

Locations