A study for evaluating effects of a single intake of the test beverage on EEG and autonomic nervous system.
- Conditions
- Healthy subjects
- Registration Number
- JPRN-UMIN000048921
- Lead Sponsor
- HUMA R&D CORP
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 24
Not provided
1.Subject who is taking medication or under medical treatment due to illness. 2.Subject who is taking foods for specified health use, foods with functional claims, health foods (including supplements) that affect the autonomic nervous system, metabolism, and sleep, and cannot stop taking them during the test period. 3.Subject who is out of the hospital due to mental disorders (depression, etc.) or sleep disorders, or who has a history of mental illness in the past. 4.Subject with a history of serious diseases such as heart, liver, kidneys, digestive organs, brain, malignant tumors, immune diseases, diabetes, etc. 5.Subject with defects in EEG and heart rate measurements (abundance chest hair, use of a pacemaker, skin rash, etc.) 6.Heavy drinker. 7.Subject who has difficulty quitting drinking from the day before the test date. 8.Subject who has extremely irregular eating habits, those who work shifts, those who work late at night, etc. 9.Subject who is participating in other clinical trials at the time of obtaining consent, and who plans to participate in other clinical trials within 4 weeks from the end of the study to the start of the main study of the study, or after consenting to participate in the study. 10.Subject who is likely to be under great stress due to moving, changing jobs, separation from close relatives, etc. within the last 3 months. 11.Subject who exercises violently on a daily basis. 12.Subject with severe PMS (premenstrual syndrome) symptoms. 13.Subject who is planning to get pregnant during the test period after the day of informed consent or is currently pregnant and lactating. 14.Subject with hay fever or allergic rhinitis (seasonal or perennial) 15.Subject who is allergic to medicines and food. 16.Subject who has or had a history of either medicine or alcohol. 17.Subject who can't keep the daily records. 18.Subject who the investigator has determined that participation in this study is inappropriate.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method