Tokyo, May 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061415) titled 'A study of the effects of guideline-referenced AI use among home-visit nurses' on April 30.

Study Type: Interventional

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

Primary Sponsor: Institute - Tekix Corporation

Condition: Condition - Not applicable; web-based simulated case task among home-visit nurses Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - The objective of this study is to examine the effects of guideline-referenced AI use on perceived mental effort, perceived task difficulty, and confidence after completing a simulated case-based task among home-visit nurses. Basic objectives2 - Others

Intervention: Interventions/Control_1 - AI group: Participants completed a simulated home-visit nursing case task involving an older adult living alone with chronic heart failure. During the task, they were allowed to use a guideline-referenced AI chat system built with NotebookLM. The system was preloaded with publicly available heart failure-related clinical guidelines and allowed participants to ask questions in natural language and refer to the generated responses. The task was completed once online. Participants were instructed not to refer to external information sources other than the AI system during the task. Interventions/Control_2 - Non-AI group: Participants completed the same simulated home-visit nursing case task once online without access to the guideline-referenced AI chat system. They were instructed not to refer to external information sources during the task.

Eligibility: Age-lower limit - Not applicable Age-upper limit - Not applicable Gender - Male and Female Key inclusion criteria - 1. Nurses currently engaged in home-visit nursing practice in Japan 2. Individuals able to read the study information and respond to the questionnaire in Japanese 3. Individuals with access to a web-enabled device for completing the task and questionnaire 4. Individuals who provided informed consent through the web-based form Key exclusion criteria - 1. Participants who did not complete the task after providing consent 2. Participants whose responses were clearly incomplete, such as missing primary outcome data Target Size - 172

Recruitment Status: Recruitment status - Completed Date of protocol fixation - 2026 Year 02 Month 05 Day Date of IRB - 2026 Year 03 Month 06 Day Anticipated trial start date - 2026 Year 03 Month 09 Day Last follow-up date - 2026 Year 03 Month 27 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070275

Disclaimer: Curated by HT Syndication.