Healthy subjects
Conditions
Interventions
None listed
Sponsors
Macromill, Inc.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Adults aged 20 years or older and under 40 years (2) Male and female working adults (3) BMI less than 30.0 (4) Non-smokers (no smoking within the past year) (5) Individuals who have a habitual alcohol consumption in their daily life (6) Users of an iPhone with iOS 16 or later, or an Android device with OS 10 or later (7) Individuals who have sufficient understanding of the purpose and details of this study, have the capacity to give consent, and can provide their own consent via electronic informed consent after receiving an adequate explanation
Exclusion criteria
Exclusion criteria: (1) Individuals currently receiving treatment with any medication or herbal medicine (occasional use allowed). (2) Individuals with a history or current diagnosis of serious diseases affecting the heart, liver, kidneys, digestive system, or other major organs. (3) Individuals with hay fever (autumn pollen) or allergic rhinitis (seasonal or perennial). (4) Individuals under dietary or exercise therapy supervised by a physician. (5) Individuals who routinely use over-the-counter drugs, quasi-drugs, Foods for Specified Health Uses, Foods with Function Claims, or supplements that may affect the autonomic nervous system, metabolism, or sleep (those who can stop use after consent and during the study may participate). (6) Individuals consuming excessive alcohol (60 g or more pure alcohol per day). (7) Individuals with extremely irregular eating habits or lifestyles, such as shift or night workers. (8) Individuals who participated in another clinical trial within one month before consent (except for psychological studies under the AQI), those currently or planning to participate during this study, or within four weeks after its completion. (9) Individuals who have experienced major life stress (for example, relocation, job change, or bereavement) within three months before consent, or are expected to during the study. (10) Individuals with known drug or food allergies. (11) Individuals unable to consume alcohol due to intolerance. (12) Individuals who are pregnant, lactating, possibly pregnant, or planning pregnancy during the study. (13) Individuals unable to wear a wrist type wearable device daily. (14) Individuals judged unsuitable for participation by the principal investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Physiological measurements using a wearable device | — |
Secondary
| Measure | Time frame |
|---|---|
| Questionnaire | — |
Countries
Japan
Contacts
Public ContactYuki Mori
Macromill, Inc. Clinical Trial Department, Life Science Division
Outcome results
None listed