- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06425965
Effect of Hybrid Simulation Method on Advanced Life Support Application of Nursing Students
March 24, 2026 updated by: Yagmur Sen, Istanbul University - Cerrahpasa
The use of simulation in nursing education is an effective way to provide professional skills and enrich learning experiences while protecting patient safety.
When the literature is examined, it is seen that simulation is frequently used in advanced life support training.
The aim of the study is to examine the effects of advanced life support training in adults, which will be carried out with high-reality simulator/model simulation, web-based simulation and hybrid simulation methods, on the knowledge and skills of nursing students.
It has been determined that training provided with hybrid simulation contributes to the professional development of students by creating individualized and interactive learning environments, and that students can more easily transfer the knowledge they have acquired in the educational environment to clinical practice.
As a hybrid simulation method in the study; It is planned to use a combination of high-reality simulator/model, which has been proven to be effective in the development of psychomotor skills, and the web-based simulation method, which is effective in creating permanent learning by allowing students to repeat more.
It is anticipated that the web-based simulation method will be effective in providing permanent learning as it gives learners the opportunity to repeat during/after the training.
Based on these assumptions, it is planned to develop an adult advanced life support training program consisting of theory and practice, in which the development of students' professional skills is supported through hybrid simulation applications, and the students are provided with the opportunity to repeat.
Since the study tests 3 different interventions, it is anticipated that it will lay the groundwork for subsequent studies and provide comprehensive information about simulation-based education practices.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
73
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 Locations
-
-
Avcılar
-
Istanbul, Avcılar, Turkey (Türkiye), 34320
- Istanbul University-Cerrahpasa, Florence Nightingale Faculty of Nursing
-
-
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
Yes
Description
Inclusion Criteria:
- To complete first aid, internal medicine nursing, surgical nursing courses,
- Volunteering to participate in the research.
- Having experienced the simulation application before
Exclusion Criteria:
- Fail the specified courses (taking FF)
- Not having taken first aid course/training before
- Not having experienced the simulation application before.
Disqualification criteria:
- Being absent for more than 20% of the theoretical part of the planned advanced life support training
- Not participating in the laboratory applications of the planned advanced life support training
- Not having completed the planned web-based simulation application
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention Group 2
The second group will receive advanced life support training with web-based simulation method.
|
The training consists of theoretical and practical training.
The length of the training is 15 hours in total, 12 hours of theoretical and 3 hours of laboratory practice.
Theoretical courses start with introductions and sharing the content of the training and aim to provide the basic professional knowledge and skills required for advanced life support practice (diagnosis of cardiac arrest, ensuring airway patency, monitoring, cardiac rhythm diagnosis, drugs used during advanced life support, advanced life support algorithm).
The laboratory practices of the training is carried out by web-based simulation method.
Students participate in the web-based simulation application developed by the researcher.
|
|
Experimental: Intervention Group 3
The third group will receive advanced life support training with a hybrid simulation method using both high reality simulator and web-based simulation.
|
The training consists of theoretical and practical training.
The length of the training is 15 hours in total, 12 hours of theoretical and 3 hours of laboratory practice.
Theoretical courses start with introductions and sharing the content of the training and aim to provide the basic professional knowledge and skills required for advanced life support practice (diagnosis of cardiac arrest, ensuring airway patency, monitoring, cardiac rhythm diagnosis, drugs used during advanced life support, advanced life support algorithm).
The laboratory practices of the training is carried out with the hybrid simulation method in which high reality simulator and web-based simulation method are applied together.
Students first apply the web-based simulation developed by the researcher.
Then they perform the practice on the high reality simulator.
|
|
Experimental: Intervention Group 1
The first group will receive advanced life support training with a high fidelity simulator.
|
The training consists of theoretical and practical training.
The length of the training is 15 hours in total, 12 hours of theoretical and 3 hours of laboratory practice.
Theoretical courses start with introductions and sharing the content of the training and aim to provide the basic professional knowledge and skills required for advanced life support practice (diagnosis of cardiac arrest, ensuring airway patency, monitoring, cardiac rhythm diagnosis, drugs used during advanced life support, advanced life support algorithm).
The laboratory practices of the training is carried out with a high reality simulator in line with the information, scenario implementation and debriefing sessions, respectively.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Advanced Life Support Knowledge Test
Time Frame: before training, immediately after training, 4 month after training
|
It was developed by the researchers in line with the literature to determine the level of knowledge of the participants about advanced life support practice.
|
before training, immediately after training, 4 month after training
|
|
Advanced Life Support Skill Checklist
Time Frame: before training, immediately after training, 4 month after training
|
It was developed by the researcher based on the European Resuscitation Council 2021 Advanced Life Support Algorithm.
|
before training, immediately after training, 4 month after training
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Student Satisfaction and Self-confidence in Learning Scale
Time Frame: immediately after training
|
The scale was developed by Jeffries and Rizzolo in 2006.
The Turkish validity and reliability study of the scale was conducted by Ünver et al. in 2015.
The scale aims to determine students' satisfaction and self-confidence towards learning in simulation environment.
The scale consists of two sub-dimensions, "Satisfaction with Current Learning" and "Confidence in Learning", and a total of 12 items.
The scale is a 5-point Likert scale (1: Strongly disagree, 2: Disagree, 3: Undecided, 4: Agree, 5: Strongly Agree) and each item is scored as 1 being the lowest and 5 being the highest.
The higher the total score obtained from the scale, the higher the student satisfaction and self-confidence in learning.
|
immediately after training
|
|
Simulation Design Scale
Time Frame: immediately after training
|
The scale was developed by Jeffries and Rizzolo in 2006 and the Turkish validity and reliability study was conducted by Ünver et al. in 2015.
The scale consists of 20 items and 2 sections.
The first part measures simulation design elements, and the second part measures how important the simulation application is for students.
An increase in the total score obtained in the first part of the scale indicates that the best simulation design elements are applied in the simulation application; an increase in the total score obtained from the second part indicates that the importance given by the student to the simulation experience is high.
|
immediately after training
|
|
Semi-structured Interview Form
Time Frame: immediately after training
|
In this study, a semi-structured interview form developed by the researchers in line with the literature was used to determine the opinions of the students participating in the Advanced Life Support in Adults Training Program about the training program.
The form consists of questions aimed at determining the theoretical content of the training program, the effectiveness of teaching methods (web-based simulation, simulation with high reality simulator, hybrid simulation), the effects of the training on learning retention, and suggestions for improving the training program.
|
immediately after training
|
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 (Actual)
December 1, 2024
Primary Completion (Actual)
July 15, 2025
Study Completion (Actual)
August 1, 2025
Study Registration Dates
First Submitted
May 17, 2024
First Submitted That Met QC Criteria
May 17, 2024
First Posted (Actual)
May 23, 2024
Study Record Updates
Last Update Posted (Actual)
March 27, 2026
Last Update Submitted That Met QC Criteria
March 24, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 641752
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
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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