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Observational study on the daily consumption of alcoholic and non-alcoholic beverages

Observational study on the daily consumption of alcoholic and non-alcoholic beverages - Observational study on the daily consumption of alcoholic and non-alcoholic beverages

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000056098
Enrollment
100
Registered
2024-11-11
Start date
2024-10-23
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy subjects

Interventions

None listed

Sponsors

Macromill, Inc.
Lead Sponsor

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 have drinking habits in daily life. 6.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. Judged by the investigator to be unsuitable for participating in this study

Design outcomes

Primary

MeasureTime frame
Lifestyle Survey

Secondary

MeasureTime frame
Beverage-related questionnaire

Countries

Japan

Contacts

Public ContactYuki Mori

Macromill, Inc. Life Science Division

yuk_mori@macromill.com080-5186-5400

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026