- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07655752
THE EFFECT OF SİMULATİON-BASED INTERPROFESSİONAL EDUCATİON ON ATTİTUDES TOWARD TEAMWORK
June 13, 2026 updated by: Fırat Seyhan, Saglik Bilimleri Universitesi
THE EFFECT OF SİMULATİON-BASED INTERPROFESSİONAL EDUCATİON ON TEAMWORK ATTİTUDES AMONG NURSİNG AND PARAMEDİC STUDENTS
Our study aims to evaluate the effect of interprofessional simulation-based learning on teamwork attitudes among nursing and paramedic students during the patient handover process.
The study sample consists of fourth-year (senior) students from the Gülhane Faculty of Nursing at the University of Health Sciences and second-year (senior) students from the Paramedic Program at the School of Health Professions.
In this study, the intervention will be conducted in two phases: the preparation phase and the implementation phase.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
56
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Fırat S SEYHAN, PhD, Assistant Professor
- Phone Number: +90 530 886 8099
- Email: firat.seyhan@sbu.edu.tr
Study Contact Backup
- Name: Esma Y YILDIZ, MsC, Research Assistant
- Phone Number: +90 544 242 70 28
- Email: 250902032@ogrenci.sbu.edu.tr
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
Nursing Student:
- Be a 4th-year (senior) student in a bachelor's degree program in nursing
- Have completed an emergency department rotation as part of the Clinical Practice I course and have finished the emergency department internship
- Having previously participated in a simulation-based practice
Paramedic Student:
- Be a second-year (final-year) student in the paramedic associate degree program
- Since the emergency department internship is completed in the first year, have completed the first-year summer internship of the Paramedic Program
- Have taken the Professional Practice-I course
- Having previously participated in a simulation-based practice
Exclusion Criteria:
Paramedic and nursing students:
- Must be a graduate of a vocational high school for health professions,
- Must have worked or currently be working in the field as a nurse or emergency medical technician
- Having previously participated in an interprofessional simulation-based practice.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Simulation-Based Interprofessional Education Group
Nursing and paramedic students in this group will participate in a simulation-based interprofessional education program.
A pre-test will be administered before the training and a post-test after the training to assess the impact on participants' attitudes toward teamwork.
|
Participants will receive theoretical training on the ATMIST (Age, Time, Mechanism, Injuries, Signs, Treatment) patient handover method.
During the simulation exercises, teams consisting of a paramedic and a nursing student will be expected to perform patient handover using the ATMIST method.
A prebriefing will be conducted before the simulation, and a debriefing using the Gather-Analyze-Summarize (GAS) model will be conducted afterward.
Simulation performances will be evaluated by researchers using checklists.
A Sociodemographic Data Collection Form and a Teamwork Attitudes Scale will be administered as a pre-test.
In the post-test, the Teamwork Attitudes Scale and the Simulation Design Scale will be administered.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Teamwork Attitudes Questionnaire
Time Frame: Baseline (pre-test), immediately after the training session (post-test)
|
The Teamwork Attitudes Questionnaire (TAS) was developed based on the Teamwork Attitudes Questionnaire (TAQ), which was created as part of the TeamSTEPPS (Team Strategies and Tools to Enhance Performance and Patient Safety) program to assess healthcare professionals' attitudes toward teamwork.
The validity and reliability study of the scale in Turkish was conducted by Yardımcı et al.
The scale consists of five subscales: team structure, leadership, situational awareness, mutual support, and communication.
Reliability analyses revealed that the Cronbach's alpha coefficients for the scale's subscales ranged from 0.70 to 0.89, demonstrating that the scale is a valid and reliable measurement tool for healthcare professionals in the Turkish population.
The minimum score that can be obtained on the scale is 28, and the maximum score is 140.
There are no reverse-scored items, and as the score increases, the level of teamwork attitude is higher.
|
Baseline (pre-test), immediately after the training session (post-test)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Simulation Design Scale
Time Frame: İmmediately after the training session (post-test)
|
The Simulation Design Scale was developed by Jeffries et al. (2006) to evaluate the design characteristics of simulation-based learning environments (19).
Its validity and reliability were established by Ünver et al. in [year].
The scale consists of 20 items and two sections.
The first section assesses the level of implementation of simulation design elements, while the second section evaluates the importance of these elements from the students' perspective.
The scale consists of five subscales: objectives and knowledge, support, problem-solving, feedback/guided reflection, and realism.
A higher score indicates a higher quality of simulation design and the student's greater emphasis on the simulation experience.
In the reliability analyses conducted, the Cronbach's alpha coefficients for the scale's sub-dimensions ranged from 0.73 to 0.86, demonstrating that the scale is a valid and reliable measurement tool for nursing students in the Turkish population.
|
İmmediately after the training session (post-test)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
June 15, 2026
Primary Completion (Estimated)
July 15, 2026
Study Completion (Estimated)
July 15, 2026
Study Registration Dates
First Submitted
June 13, 2026
First Submitted That Met QC Criteria
June 13, 2026
First Posted (Actual)
June 18, 2026
Study Record Updates
Last Update Posted (Actual)
June 18, 2026
Last Update Submitted That Met QC Criteria
June 13, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 2026-066
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data will not be shared to ensure the confidentiality of the participants and to comply with institutional ethical guidelines.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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