Preliminary Exploration of Applying Multi-person Simulation Training to Improve Nurse-led Burn and Scald Nursing Care

Chimei Medical Center

Status: Completed

Conditions: High Fidelity Simulation Training; Virtual Reality

Treatments: Other: Multi-person high-fidelity simulation scenario training; Other: Multi-person virtual reality simulation scenario training

Study type: Interventional

Funder types: Other

Identifiers

NCT05493774

11105-012

Details and patient eligibility

About

The purpose of this study was to compare the learning performance of trainees before and after learning burns and scald nursing care by applying the burns and scald virtual reality (VR) training module multi-person interactive training in different places and the traditional training model with a high-fidelity patient.

Full description

The clinical instructors, standard practice nurses, training content, and assessment process were the same for the experimental and control groups, except for the training methods of the interventions. A pre-recorded instructional video on burn care was provided to each participant one week prior to the experiment for self-study. The experiment procedure includes research description, pre-test and pre-test questionnaire (about 10 minutes), VR hands-on teaching or environment familiarization phase (about 10 minutes), multi-person simulation training (about 15 minutes) and post-test debrief (about 5 minutes), post-test and questionnaire (about 10 minutes). After completing all experiments, the collected data will be analyzed by the researcher using SPSS version 22.0 for descriptive, t-test, and other statistical analyses.

Enrollment: 60 patients

Sex: All

Ages: 20+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. people who are above 20 years old, with a nurse practitioner certificate and an ACLS or AHA certificate within the validity period.
2. people who are interested in learning the role of a team leader in burn and scald care.
3. people who have never used an interactive virtual reality (VR) environment device.

Exclusion criteria

1. people who are prone to vertigo or poor balance and are prone to motion sickness.
2. people with a history of epilepsy.
3. eye surgery or injury within the past 6 months.
4. people with facial wounds that prevent them from wearing VR glasses.

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

---

60 participants in 2 patient groups

Experimental group

Experimental group

Description:

Virtual reality

Treatment:

Other: Multi-person virtual reality simulation scenario training

Control group

Active Comparator group

Description:

High Fidelity Simulation Training

Treatment:

Other: Multi-person high-fidelity simulation scenario training