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Clinical Trials/NCT05493774
NCT05493774
Completed
Not Applicable

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

Chimei Medical Center1 site in 1 country60 target enrollmentStarted: May 22, 2023Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Chimei Medical Center
Enrollment
60
Locations
1
Primary Endpoint
Self-reported measure of satisfaction of learning

Overview

Brief Summary

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.

Detailed 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

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

Exclusion Criteria

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

Outcomes

Primary Outcomes

Self-reported measure of satisfaction of learning

Time Frame: Post-instruction (immediately after completing simulation scenario training)

The satisfaction of learning scale included 9 items. Each item was scored on a five-point Likert-type scale ranging from 1 (strongly disagree) to 5 (strongly agree). The total score ranged from 9 to 45 and a higher score indicated a higher level of satisfaction with the learning intervention in burns and scald nursing care.

Change in knowledge of burn and scald nursing care scale

Time Frame: Pre- and post-instructional design (immediately before conducting and after completing simulation scenario training)

There were 10 items to evaluate the participants' knowledge of the burn and scald nursing care scale. Each item had four response options. The total score ranged from 0 to 10 and a higher score indicates a higher level of knowledge of burn and scalds nursing care.

Change in motivation and attitude toward learning and personal self-efficacy scale

Time Frame: Pre- and post-instructional design (before conducting and immediately after completing simulation scenario training)

The motivation and attitude toward learning and personal self-efficacy scale included 21 items. Each item was scored on a five-point Likert-type scale ranging from 1 (strongly disagree) to 5 (strongly agree). The total score ranged from 21 to 105 and a higher score indicated a positive motivation and attitude toward learning and a higher level of personal self-efficacy in burn and scald nursing care.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Chimei Medical Center
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ying-Li Lee

Principal Investigator

Chimei Medical Center

Study Sites (1)

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