Effects of Augmented Reality-based Rapid Blood Transfusion (Level-1®)
1 other identifier
interventional
42
1 country
1
Brief Summary
The goal of this clinical trial is to compare the effectiveness of AR-based training with traditional guideline-based self-learning in practical nurses without prior Level-1® experience. The main questions it aims to answer are: Does AR-based training using Microsoft HoloLens 2® improve clinical performance compared to traditional guideline-based self-learning? Does AR-based training affect self-efficacy and educational satisfaction compared to traditional methods? Participants will: Receive AR-based training using Microsoft HoloLens 2® (experimental group) Follow traditional guideline-based self-learning (control group) Researchers will compare the AR-based training group to the traditional self-learning group to see if AR-based training leads to better clinical performance, higher self-efficacy, and greater educational satisfaction.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 17, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 5, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
September 5, 2023
CompletedFirst Submitted
Initial submission to the registry
June 12, 2024
CompletedFirst Posted
Study publicly available on registry
July 18, 2024
CompletedJuly 18, 2024
June 1, 2024
2 months
June 12, 2024
July 9, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Clinical Competency
This measurement assesses nurses' clinical competency in rapid infusion procedures. It includes evaluation of learning time, performance time, accuracy, and assistance requests.
before training, immediately after training
Secondary Outcomes (1)
Self-efficacy
efore training, immediately after training
Other Outcomes (1)
Educational Satisfaction Evaluation
Educational satisfaction will be assessed immediately after the completion of the training program.
Study Arms (2)
AR-based Training Group
EXPERIMENTALPractical nurses in this arm receive AR-based training using Microsoft HoloLens 2®. This training method incorporates augmented reality technology to provide immersive and interactive learning experiences, enhancing their proficiency in device utilization.
Traditional Self-Learning Group
SHAM COMPARATORPractical nurses in this arm follow traditional guideline-based self-learning methods without augmented reality technology. They rely on conventional educational materials and guidelines for learning device utilization skills.
Interventions
Practical nurses in this group receive AR-based training using Microsoft HoloLens 2®. This training method incorporates augmented reality technology to provide immersive and interactive learning experiences, enhancing their proficiency in device utilization.
Practical nurses in this group follow traditional guideline-based self-learning methods without augmented reality technology. They rely on conventional educational materials and guidelines for learning device utilization skills.
Eligibility Criteria
You may qualify if:
- Willingness to participate voluntarily and understanding of the study's purpose.
- No prior experience with the Level-1® rapid infusion system.
You may not qualify if:
- Prior experience with the Level-1® rapid infusion system.
- Inability to comprehend the study's purpose or express voluntary participation.
- Inability to attend required training and evaluations.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Samsung Medical Center
Seoul, 06351, South Korea
Study Officials
- STUDY CHAIR
meonghi son, MD
Samsung Medical Center
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 12, 2024
First Posted
July 18, 2024
Study Start
July 17, 2023
Primary Completion
September 5, 2023
Study Completion
September 5, 2023
Last Updated
July 18, 2024
Record last verified: 2024-06