Tokyo, Dec. 10 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059953) titled 'Development and Efficacy of a Person-Centered Care-Based Metaverse Dementia Nursing Platform' on Dec. 10.

Study Type: Interventional

Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled

Primary Sponsor: Institute - Hamamatsu University School of Medicine

Condition: Condition - no Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - The purpose of this study is to examine the efficacy of a Metaverse Dementia Nursing Platform (including elearning and video materials) based on person-centered care, utilizing the Metaverse a three dimensional digital virtual space where users enjoy interactive communication and activities via the internet and to evaluate its effectiveness, including educational program interventions. Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - Metaverse Dementia Nursing Platform Based on Person-Centered Care Using the Metaverse (e-learning, video materials, etc.)

Eligibility: Age-lower limit - 20 years-old = Gender - Male and Female Key inclusion criteria - Target patients meeting all the following criteria: 1. All full-time nurses (approximately 700) at Juntendo University Shizuoka Hospital (633 beds: 7:1 nursing ratio) 2.Those involved in the treatment and nursing care of elderly dementia patients 3.Individuals for whom informed consent to participate in this research, given of their own free will, has been obtained 4.Individuals able to connect to the internet via their personal PC and acc Key exclusion criteria - The following individuals shall not be included in this study: 1. Professionals from hospitals other than the designated study hospital 2. Professionals not involved in the treatment or care of elderly individuals with dementia 3. Individuals working part-time, on maternity leave, or on leave of absence 4. Individuals for whom research participation consent could not be obtained Target Size - 200

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2025 Year 08 Month 01 Day Date of IRB - 2025 Year 08 Month 21 Day Anticipated trial start date - 2025 Year 12 Month 01 Day Last follow-up date - 2026 Year 12 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000068577

Disclaimer: Curated by HT Syndication.