Tokyo, Sept. 29 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059185) titled 'A Study on the Effects of Introducing the AI Meal Logging App "FoodLogAthl" to Improve Dietitian Efficiency and Reduce Patient Burden' on Sept. 29.

Study Type: Interventional

Study Design: Basic Design - n-of-1 Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled

Primary Sponsor: Institute - Kanagawa University of Human Services

Condition: Condition - Type 2 diabetes mellitus, Hypertension, Dyslipidemia Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - The primary objective of this study is to verify in a clinical setting whether the use of an AI meal logging app can reduce both the workload of dietitians and the documentation burden of patients in the practice of optimal nutritional assessment. Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - Intervention: Use of the AI-powered dietary recording application, "FoodLogAthl". Duration: The intervention phase (Phase B) lasts for two consecutive months. Within each month, participants record their diet for 5 days, resulting in a total of 10 recording days over the intervention period. Dosage: The "dosage" is the act of using the application. Participants are required to take and upload one photograph per meal, including snacks. Frequency: Dietary recording is performed on 5 days per month for two months. The detailed nutritional assessment by the registered dietitian is performed once per month, following the face-to-face consultation.

Eligibility: Age-lower limit - 20 years-old

Gender - Male and Female Key inclusion criteria - Adults aged 20~75 years attending Zushi Orthopedic and Internal Medicine Clinic who have been diagnosed with type 2 diabetes, hypertension, dyslipidemia, or any combination of these conditions. Determined by the attending physician to be eligible for nutritional counseling by a registered dietitian. Able to perform basic operations on their own smartphone (iOS 14.0 or later/Android 6.0 or later) and agree to install the study application. Key exclusion criteria - Individuals with severe renal impairment (eGFR 30 mL/min/1.73m2) or eating disorders, or those judged by the principal investigator or attending physician to be unsuitable for the dietary recording method used in this study.Individuals with cognitive decline or other conditions making it difficult to understand the study or operate the application independently (HDS-R score 20, or as determined by the attending physician).Individuals from whom informed consent cannot be obtained. Target Size - 12

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2025 Year 09 Month 30 Day Anticipated trial start date - 2025 Year 11 Month 01 Day Last follow-up date - 2027 Year 03 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067697

Disclaimer: Curated by HT Syndication.