Healthy subjects
Conditions
Interventions
None listed
Sponsors
Macromill, Inc.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1)Aged 20 to under 40 at the time of informed consent. (2)Japanese male and female (3)BMI of less than 30.0 kg/m2 (4)Those who does not smoke (who have not been smoking for the last year) (5)Those who frequently purchase beverages in daily life. (6)Those who are using an iPhone with iOS 16 or late. (7)Those who have received a thorough explanation of the purpose and content of this study, have the capacity to consent, fully understand the content, and can provide their consent through electronic informed consent.
Exclusion criteria
Exclusion criteria: (1)Taking medication or Chinese medication (except for the dugs as needed) (2)Current of history of serious diseases such as heart, liver, kidney, gastrointestinal tract. (3)Those who has pollinosis (autumn pollen) or allergic rhinitis (seasonal/perennial) (4)Under diet of exercise therapy under the supervision of a doctor (5)Those who regularly uses any commercially available drug and quasi-drug, food for specified health use, food that affects autonomic nervous system, and sleep (however, the person will be eligible if he/she can stop using it during the study period after provision of the informed consent) (6)Excessive consumption of alcohol (alcohol equivalent 60g or more /day) (7)Irregular diet, shift worker, night shift, irregular life rhythm (8)Those who has participated another clinical study within 1 month prior to provision of the informed consent , other than the psychological evaluation study conducted by AQI,or is currently participating in it, or will participate in it during the study period or within 4 weeks after the end of the study (9)Those who will be possibly under significant stress of any life event such as moving, changing his/her job, and separation from a close relative, within 3 months prior to provision of the informed consent, or will have such a life event during the study period (10)Current of history of drug and/or food allergies (11)Those who is unable to drink alcohol constitutionally (12)Those who are breastfeeding, pregnant, possibly pregnant, or intend to become pregnant during the study period. (13)Those who have difficulty wearing a wristwatch-type wearable device on a daily basis. (14)Judged by the investigator to be unsuitable for participating in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Psychological evaluation questionnaire | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Physiological measurements using a wearable device 2. Beverage-related questionnaire | — |
Countries
Japan
Contacts
Public ContactYuki Mori
Macromill, Inc. Life Science Division
Outcome results
None listed