N/A(healthy adults)
Conditions
Interventions
None listed
Sponsors
Morinaga & Co., Ltd.
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1)Toshiba corporate cohort registrants who have provided consent to participate in this study 2)Male individuals aged 35 or older but under 60 at the start of the study 3)Individuals who drink alcohol 2 to 5 times per week 4)Individuals whose single drinking session contains 20g or more of alcohol 5)Individuals with no smoking habit 6)Healthy individuals not undergoing regular medical treatment or taking medication 7)Individuals who have never experienced skin issues (such as rashes, eczema, redness) from using cosmetics or quasi-drugs and do not consider their skin sensitive 8)Individuals able to wear Libre 2 for approximately 2 weeks (maximum 14 days) and maintain a log regarding alcohol consumption, complete a hangover questionnaire, and record snacking and hunger levels 9)Individuals employed at Toshiba headquarters at the study start date who can come to a designated location at Toshiba headquarters during non-working hours (lunch break) for Libre 2 application and data retrieval completion 10)Individuals who can comply with the Libre 2 service regulations and instruction manual contents 11)Individuals who can personally prepare a smartphone (iPhone or Android) meeting the requirements for FreeStyle Libre Link compatibility 12)Individuals with no scheduled MRI, X-ray, or CT scans during the Libre wear period 13)Individuals with no scheduled airplane travel during the Libre wear period
Exclusion criteria
Exclusion criteria: 1)Individuals who may change their lifestyle habits during the study period 2)Individuals who participated in another clinical trial involving interventions within one month prior to registering their consent to participate in this study, or who plan to participate in another clinical trial involving interventions during the study period 3)Individuals who currently have, or have had within the past three months, a habit of continuously consuming foods with functional claims, health foods, or supplements that claim to affect blood glucose levels, or who plan to consume such products during the study period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood glucose changes | — |
Secondary
| Measure | Time frame |
|---|---|
| Record Log, Questionnaire | — |
Countries
Japan
Contacts
Public ContactHiroko Uchida
Morinaga & Co., Ltd. Health Science and Research Center, R&D institute
Outcome results
None listed