Development and validation of a mixed reality simulation education program for new nurses

Improving the effectiveness of nursing care for patients with dyspnea: Development and validation of a mixed reality simulation education program for new nurses

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0009087

Enrollment

Registered

2023-12-29

Start date

2023-10-10

Completion date

Unknown

Last updated

2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others : The control group will receive the existing education for new nurses on patients with dyspnea, while the intervention group will be applied with a Mixed Reality (MR) simulation education prog

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The participants of this study will be new nurses who have joined C University Hospital in G Metropolitan City and will be conveniently sampled among nurses who understand the purpose of the study and have agreed to participate. The sample size will be calculated using G*Power 3.1.9.7, and referring to the effect size of the study by Hwang Sun-young and Choi Hee-seung[20], considering a significance level (?=.05), effect size (f=0.25), test power (1-ß=.95), number of groups 2, number of repeated measurements 3 times, and maintaining a medium effect size of 0.5 in correlation analysis between points, a minimum of 44 participants in total is required, necessitating 22 participants per group. Considering the data collection period and the dropout rate due to the resignation of new nurses, 60 people will be recruited. Numbers will be assigned in order to the list of new nurses who wished to participate in this study, and two groups will be randomly assigned using the online service provided by the Social Psychology Network's research randomizer (www.randomizer.org). Focus group interviews will be conducted with 17 people who wish to participate from the experimental group.

Exclusion criteria

Exclusion criteria: Individuals who refuse to participate in this study, nurses with clinical experience.

Design outcomes

Primary

Measure	Time frame
Clinical competency in nursing patients with dyspnea.	—

Secondary

Measure	Time frame
Confidence in performing nursing for patients with dyspnea.;Knowledge of nursing for patients with dyspnea;Problem-solving ability;Educational satisfaction	—

Countries

Korea, Republic of

Contacts

Public ContactHye Won Jeong

Chonnam National University Hospital

y2k331646@gmail.com+82-62-220-4685

Outcome results