Tokyo, March 24 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061001) titled 'Development of a novel Augmented Reality (AR) educational tool for training in endotracheal intubation' on March 24.

Study Type: Interventional

Study Design: Basic Design - Parallel Randomization - Randomized Blinding - Open -no one is blinded Control - Active

Primary Sponsor: Institute - The University of Tokyo Hospital

Condition: Condition - Airway management Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - The objective of this study is to develop a novel educational tool for endotracheal intubation using augmented reality (AR) technology and to evaluate its effectiveness in skill acquisition. Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - Participants in the intervention group will first learn the endotracheal intubation procedure using 2D instructional videos and printed materials, followed by guidance on equipment usage. Subsequently, they will receive direct instruction and engage in supplemental learning using a 3D AR model of endotracheal intubation. Interventions/Control_2 - Participants in the control group will learn the endotracheal intubation procedure using only 2D instructional videos and printed materials, followed by guidance on equipment usage.

Eligibility: Age-lower limit - 18 years-old <= Age-upper limit - Not applicable Gender - Male and Female Key inclusion criteria - Students in the MD (Doctor of Medicine) program at the Faculty of Medicine, The University of Tokyo Key exclusion criteria - Individuals who must avoid external physical strain on the head and neck (e.g., those with a history of trauma or cervical spondylosis).

Individuals who have previously experienced motion sickness or physical discomfort when using AR or similar technologies.

Individuals with prior experience in performing endotracheal intubation procedures. Target Size - 60

Recruitment Status: Recruitment status - Completed Date of protocol fixation - 2025 Year 01 Month 21 Day Date of IRB - 2025 Year 01 Month 20 Day Anticipated trial start date - 2025 Year 05 Month 06 Day Last follow-up date - 2025 Year 07 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000069797

Disclaimer: Curated by HT Syndication.