None
Conditions
Interventions
During Week 1, participants will undergo an observation period without the use of digital dietary management tools. During Week 2, they will engage in a dietary management period using a generative AI
Sponsors
Kanazawa University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Adults aged 20 to 75 years 2) Able to perform basic smartphone or PC operations 3) Able to understand the study and provide written informed consent 4) Able to complete the 2-week observation period 5) Not meeting any exclusion criteria
Exclusion criteria
Exclusion criteria: 1) Women who are pregnant or breastfeeding 2) Patients with diabetes receiving insulin therapy 3) Individuals who have undergone surgery requiring general anesthesia within the past 3 months 4) Individuals currently under treatment for severe psychiatric disorders 5) Individuals judged to have insufficient cognitive ability to understand the study and provide appropriate informed consent 6) Individuals for whom placement of the FreeStyle Libre 2 sensor is difficult (e.g., severe skin disease, wounds or infection at the application site, history of adhesive allergy, or physical difficulty in sensor placement) 7) Individuals currently receiving treatment for eating disorders 8) Individuals on dialysis or with urinary protein of 1+ or greater 9) Individuals with severe hepatic dysfunction (Child-Pugh class C) 10) Individuals who have participated in another clinical study or trial within the past 1 month 11) Individuals judged by the principal investigator to be inappropriate for participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) Body Weight Change 2) Continuous Glucose Monitoring Parameters | — |
Countries
Japan
Contacts
Public ContactMitsuhiro Kometani
Kanazawa University Department of Health Promotion and Medicine of the Future
Outcome results
None listed