JPRN-UMIN000048600
Completed
未知
Effi cacy test of plant extract on sleep dissatisfi ed people - Sleep test
WELLPHARMA Inc.0 sites20 target enrollmentAugust 5, 2022
ConditionsHealthy adults
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Healthy adults
- Sponsor
- WELLPHARMA Inc.
- Enrollment
- 20
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •\-Currently receiving treatment (including medication) for any disease \-Subjects who have been diagnosed as having a sleep disorder such as insomnia or sleep apnea syndrome, and are taking drugs such as sleep inducers or insomnia medications (including OTC drugs as well as prescription drugs),or receiving treatment with CPAP or mouthpieces, etc. \-Those who regularly consume foods for specified health uses, foods with functional claims, or other foods/beverages with possible functional properties. \-Subjects with a BMI over 30 (severely obese) \-Subjects who are primarily responsible for the care of persons in need of nursing care or infants. \-All who are unable to sleep alone on a single bedding (e.g., futon or bed) during the study period. \-A person who is not able to comply with the gentle sleep control (going to bed within Plus or minus 2 hours of the reported bedtime and waking up within Plus or minus 2 hours of the reported waking time) during the test period. \-Candidates who cannot avoid drinking alcohol and consuming caffeinated beverages (sencha, black tea, coffee, caffeinated beverages, etc.) after 6:00 p.m. during the EEG measurement period and the day before the measurement period. \-Consistently consumes more than adequate alcohol (average daily alcohol consumption of approximately 20 g of pure alcohol or less). \-Consentee who is unable to complete the EEG measurement and the sleep diary/OSA sleep questionnaire according to the schedule. \-Participants who have participated or will participate in other clinical trials in the month prior to the date of consent \-Other individuals who are deemed by the physician to be inappropriate to participate in the study.
Outcomes
Primary Outcomes
Not specified
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