- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05629663
Utilizing of Augmented Reality Technology Education Program for Nurse
Utilizing of Augmented Reality Technology for Development, Application and Evaluation on Nurse Education Program
Study Overview
Status
Intervention / Treatment
Detailed Description
As patient-centered nursing education is considered more important, the amount of nursing education required is also increasing. In addition, the safety of the educational environment is important for nurses' application education to various clinical environments. In the past, simulation education, which generally expects learning effects through practice and motivation, was mainly conducted. However, in the COVID-19 situation, it has become difficult for educators and educators to gather in one space to conduct clinical education.[4] Based on the need for alternatives to this, The investigators devised a nurse education program using various new technologies.
Recently, virtual training systems are being developed in various application fields thanks to the development of augmented reality and virtual reality. In particular, medical training and clinical application have become important since the recent international epidemic of COVID-19. The strength of new technologies such as Augmented Reality (AR) has enabled various programs for education and healthcare that have overcome the limitations of time and space. Augmented reality is already being applied to self-directed learning in various areas, which provides learners with a highly immersive learning environment so that medical personnel can receive more accurate and precise medical education in the field.
The investigators tried to develop an augmented reality technology-based program that can provide training to nurses using the Headmount display device, and to find out the evaluation that reaches usability and satisfaction after applying it to educators.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Seoul, Korea, Republic of, 06351
- Samsung Medical Centre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Medical staff who have participated, trained or trained in the production of ventilator/ECMO training programs using HoloLens 2
- A person who has agreed to voluntarily participate in the study through the recruitment notice
Exclusion Criteria:
- Medical staff who participate, train, or have not been trained in the production of ventilator/emo education programs using HoloLens 2
- Medical staff who participated, trained, uneducated, or abandoned in the production of ventilator/emo education programs using HoloLens 2 If you disagree with the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: AR program group
participants in the AR group were guided by AR-based instructions and requested assistance with the head-mounted device.
|
The AR instructions were developed as a step-by-step guide, utilizing the dynamic 365 Guide (Software, Microsoft Corporation, Redmond, WA, USA).
The AR instructions were delivered using the Microsoft HoloLens 2.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Device Usability and Feasibility Evaluation
Time Frame: day1
|
Semi-structured interviews will be conducted to evaluate the feasibility and usability of the device.
The interview will focus on user experiences, operational feasibility, and feedback on device design and functionality.
The questions will assess ease of use, clarity of instructions, and perceived benefits.
|
day1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
System usability scale
Time Frame: day1
|
survey for System Usability Scale.
a five-point scale(1 point to 5 point), High scores can be positive for each question, and low scores can be positive.
|
day1
|
|
Technology acceptance scale
Time Frame: day1
|
It consists of 15 questions that assess trends in the latest technology with questions on a scale of 1 to 7.
|
day1
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2022-08-079
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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