Tokyo, Oct. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059052) titled 'A Cluster Randomized Controlled Trial on the Effectiveness of Real-Time Feedback and Video-Assisted Dispatch Systems for Cardiopulmonary Resuscitation Education in Laypersons' on Oct. 1.

Study Type: Interventional

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

Primary Sponsor: Institute - Kobe University Graduate School of Medicine

Condition: Condition - Not applicable Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - This study aims to examine the effectiveness of first aid training using real-time feedback manikins on the quality of bystander cardiopulmonary resuscitation (CPR), as well as the effectiveness of video-assisted dispatch systems in providing supplementary guidance during bystander CPR. Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - Training using feedback manikins(QCPR manikins) Interventions/Control_2 - Video-assisted CPR guidance via a video dispatch system

Eligibility: Age-lower limit - 18 years-old <= Age-upper limit - Not applicable Gender - Male and Female Key inclusion criteria - 1. Non-healthcare professionals who provide informed consent to participate in the study 2. Participants in first aid training courses conducted by the Kobe City Fire Bureau and Kobe Gakuin University 3. Individuals aged 18 years or older, regardless of sex 4. Willingness to participate in Study 2 (evaluation of the video-assisted dispatch system) Key exclusion criteria - 1. Healthcare professionals or individuals with previous work experience as healthcare professionals 2. Individuals with severe visual, auditory, or upper limb impairments that make assessment or intervention implementation significantly difficult 3. Individuals with cognitive impairment that prevents adequate understanding of the study or provision of informed consent 4. Individuals unable to understand explanations provided in Japanese 5. Any other individuals deemed inappropriate for study participation by the principal investigator or co-investigators Target Size - 180

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2025 Year 09 Month 01 Day Anticipated trial start date - 2025 Year 10 Month 01 Day Last follow-up date - 2026 Year 04 Month 01 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067548

Disclaimer: Curated by HT Syndication.