Low-fidelity vs High-fidelity Simulation for Arterial Blood Gas Testing Knowledge
This study aims to evaluate how different types of simulation training, low-fidelity versus high-fidelity, affect the knowledge and practices of healthcare professionals during arterial blood gas testing.
High-fidelity interprofessional simulation
+ Low-fidelity interprofessional simulation
Behavior
Other Study
Summary
Study start date: March 1, 2026
Actual date on which the first participant was enrolled.This study aims to compare two different methods of teaching students how to perform and understand arterial blood gas (ABG) testing. ABG testing is a crucial procedure for determining the levels of oxygen and carbon dioxide in the blood, which can help diagnose various respiratory and metabolic conditions. The study involves medical and nursing students, who will be divided into groups using either high-fidelity or low-fidelity simulation techniques. High-fidelity simulations use more advanced technology and realistic scenarios, while low-fidelity simulations are simpler. This study is important as it seeks to identify the most effective teaching method for students, ensuring that future healthcare providers are well-prepared to conduct and interpret ABG tests accurately. Participants in the study will first provide consent and complete an initial questionnaire. They will watch an educational video explaining the ABG test, including how it is performed and how to interpret the results. Following the video, students are assigned to either a high-fidelity or low-fidelity simulation group. During the simulations, observers will evaluate how well students perform the test. After the simulation exercises, students will attend a debriefing session to discuss their experiences and learning. Finally, they will complete a post-simulation questionnaire to provide feedback on the training they received. This structured process is designed to assess the effectiveness of each teaching method in enhancing students' knowledge and skills in ABG testing.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.36 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * Early-career students (First-year Nursing Bachelor's Degree; second-year Medicine \& Surgery Degree) * Regularly enrolled in their courses (attended at least 70% of classes) * Proficient in English (reading and speaking) * Aged 18 years or older Exclusion Criteria: * Students who have previously taken classes on arterial blood gas sampling * Those who have prior work experience as healthcare professionals (e.g., laboratory technicians, phlebotomists) * Students who have previously experience in interprofessional learning activities * Students who have previously experience in the simulation center
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
University of Torino - Department of Clinical and Biological Sciences
Orbassano, ItalyOpen University of Torino - Department of Clinical and Biological Sciences in Google Maps