A study to investigate the efficacy and dose response of Euglena by questionnaires for a measure of the subjective well-being
Not Applicable
- Conditions
- Healthy individuals
- Registration Number
- JPRN-UMIN000037200
- Lead Sponsor
- everage Brain Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 210
Inclusion Criteria
Not provided
Exclusion Criteria
1)Subjects who are under pharmacological treatment for chronic disorders, especially subjects who take Warfarin 2)Subjects who have histories of mental disorders (Depression etc.) 3)Subjects work irregular hours on the night shift or irregular shift 4)Subjects who had participated in other clinical trials or monitoring studies within 1 month 5)Subjects who have intolerance to study food substance 6)Subjects who are in pregnancy, lactation, or who are willing to become pregnant 7)Subjects who are ineligible due to the chief inspector's judgment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Questionnaires for subjective well-being or other QOL scales
- Secondary Outcome Measures
Name Time Method