NCT06425965

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
73

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Dec 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 17, 2024

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 23, 2024

Completed
6 months until next milestone

Study Start

First participant enrolled

December 1, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2025

Completed
17 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2025

Completed
Last Updated

March 27, 2026

Status Verified

March 1, 2026

Enrollment Period

8 months

First QC Date

May 17, 2024

Last Update Submit

March 24, 2026

Conditions

Keywords

simulationAdvanced life supportNursing educationNursing studentWeb-based simulationHigh fadility

Outcome Measures

Primary Outcomes (2)

  • Advanced Life Support Knowledge Test

    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

    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 Outcomes (3)

  • Student Satisfaction and Self-confidence in Learning Scale

    immediately after training

  • Simulation Design Scale

    immediately after training

  • Semi-structured Interview Form

    immediately after training

Study Arms (3)

Intervention Group 1

EXPERIMENTAL

The first group will receive advanced life support training with a high fidelity simulator.

Other: Advanced life support training with high fidelity simulator

Intervention Group 2

EXPERIMENTAL

The second group will receive advanced life support training with web-based simulation method.

Other: Advanced life support training with web-based simulation

Intervention Group 3

EXPERIMENTAL

The third group will receive advanced life support training with a hybrid simulation method using both high reality simulator and web-based simulation.

Other: Advanced life support training with hybrid simulation

Interventions

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.

Intervention Group 1

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.

Intervention Group 2

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.

Intervention Group 3

Eligibility Criteria

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

You may qualify if:

  • To complete first aid, internal medicine nursing, surgical nursing courses,
  • Volunteering to participate in the research.
  • Having experienced the simulation application before

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul University-Cerrahpaşa, Florence Nightingale Faculty of Nursing

Istanbul, Avcılar, 34320, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant

Study Record Dates

First Submitted

May 17, 2024

First Posted

May 23, 2024

Study Start

December 1, 2024

Primary Completion

July 15, 2025

Study Completion

August 1, 2025

Last Updated

March 27, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations