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Clinical Trials/NCT06776211
NCT06776211
Completed
Not Applicable

Effectiveness of Virtual Reality and Low-Reality Simulation Application in Neonatal Resuscitation Skills Training

Saglik Bilimleri Universitesi1 site in 1 country80 target enrollmentJanuary 10, 2025

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Saglik Bilimleri Universitesi
Enrollment
80
Locations
1
Primary Endpoint
Neonatal Resuscitation Information Form
Status
Completed
Last Updated
8 months ago

Overview

Brief Summary

This research was designed to investigate the effectiveness of virtual reality and low reality simulation applications in neonatal resuscitation skills training.

Detailed Description

The research universe will consist of fourth year students studying at the Department of Midwifery, Hamidiye Faculty of Health Sciences (HSBF), Health Sciences University (SBU) in the academic year 2024-2025 (N: 80). In the preparation phase of the research, the literature on neonatal resuscitation will be reviewed by the researchers and the topic will be translated into an 8-week power point presentation. The 2-hour training content will also include case discussion and video demonstration of skills. Randomisation of the study Students who volunteer to participate in the study will be allocated to the intervention and control groups using computerised simple random sampling. The study will use computer-assisted randomisation and students will be randomly assigned to the intervention and control groups using the program with the URL address https://www.randomizer.org. By dividing the students into two groups as Virtual Reality Simulation Application and Low Reality Simulation Application, the students will be given an "Introductory Information Form", "Neonatal Resuscitation Information Form" and "Neonatal Resuscitation Skill Assessment Form". In this planned experimental pre-test and post-test design and control group study, students were divided into Virtual Reality (n₁=40) and Low Reality Simulation (n₂=40) groups. Each stage of the study and any applications to be made will be explained and a voluntary informed consent form will be obtained from each student. Students will be assessed 4 weeks after the pre-test, post-test and application.

Registry
clinicaltrials.gov
Start Date
January 10, 2025
End Date
August 29, 2025
Last Updated
8 months ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Leyla Kaya

Assoc. Prof.

Saglik Bilimleri Universitesi

Eligibility Criteria

Inclusion Criteria

  • Volunteer to participate in the research.
  • Be an active student in the 4th year of the Midwifery Department of Hamidiye Health Sciences Faculty, University of Health Sciences.
  • Attend theoretical classes regularly.

Exclusion Criteria

  • Being a passive student in the 4th year of the Midwifery Department of Hamidiye Health Sciences Faculty, University of Health Sciences.
  • Not meeting the inclusion criteria.
  • Having attended the Neonatal Resuscitation Certificate Training or Course.

Outcomes

Primary Outcomes

Neonatal Resuscitation Information Form

Time Frame: Follow-up test, 4 weeks after the post-test was administered

It is based on the General Directorate of Public Health, Newborn Resuscitation/Neonatal Resuscitation Programme (NRP) Certified Practitioner Training Programme.

Neonatal Resuscitation Skills Assessment Form

Time Frame: Follow-up test, 4 weeks after the post-test was administered

It is based on the General Directorate of Public Health, Newborn Resuscitation/Neonatal Resuscitation Programme (NRP) Certified Practitioner Training Programme.

Study Sites (1)

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