- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05493774
Preliminary Exploration of Applying Multi-person Simulation Training to Improve Nurse-led Burn and Scald Nursing Care
August 28, 2024 updated by: Ying-Li Lee, Chimei Medical Center
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.
Study Overview
Status
Completed
Conditions
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 Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Tainan, Taiwan, 710
- Chi Mei Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
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.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
Virtual reality
|
Using multi-person virtual reality simulation scenario training to evaluate the learning effectiveness of nursing care for emergency burn and scald patients.
|
|
Active Comparator: Control group
High Fidelity Simulation Training
|
Using multi-person high-fidelity simulation scenario training to evaluate the learning effectiveness of nursing care for emergency burn and scald patients.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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.
|
Pre- and post-instructional design (immediately before conducting and after completing simulation scenario training)
|
|
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.
|
Pre- and post-instructional design (before conducting and immediately after completing simulation scenario training)
|
|
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.
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Post-instruction (immediately after completing simulation scenario training)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 22, 2023
Primary Completion (Actual)
October 20, 2023
Study Completion (Actual)
October 20, 2023
Study Registration Dates
First Submitted
August 1, 2022
First Submitted That Met QC Criteria
August 6, 2022
First Posted (Actual)
August 9, 2022
Study Record Updates
Last Update Posted (Actual)
August 29, 2024
Last Update Submitted That Met QC Criteria
August 28, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 11105-012
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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