A study for the effect of intake of ONO-SR/AST-DA on sleep
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000041059
- Lead Sponsor
- TTC Co., Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 80
Not provided
1. Subjects who are currently receiving medication, dietary guidance, or exercise therapy 2. Subjects who perform an act for the improvement of the fatigue, the quality of the sleep, and stress 3. Subjects who were under treatment or have a history of serious diseases 4. Subjects who have history of mental illness, chronic fatigue syndrome, insomnia 5. Subjects who are under treatment or a history of sleep apnea syndrome or are strongly suspected of having sleep apnea syndrome 6. Subjects with nocturnal urination 7. Subjects who are likely to cause skin irritation due to electrode adhesive pads 8. Subjects who have a disease that requires constant medication, subjects with serious diseases that require medication, and subjects with a history of serious diseases 9. Subjects who perform an act for the improvement of the fatigue, the quality of the sleep and stress 10. Subjects who constantly use food richly containing involvement ingredient 11. Subjects who engage in manual labor 12. Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire 13. Subjects who plan to travel abroad or travel abroad during the research period, or who plan to travel on long domestic business trips or domestic trips for more than one week in a row 14. Subjects who have experienced abnormal clinical test values or cardiopulmonary function and have been judged to have problems participating in the study 15. Subjects at risk of developing allergy in relation to the study 16. Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination 17. Subjects who have participated in other clinical study within the last one month prior to the current study 18. Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating. 19. Subjects who are judged as unsuitable for the study by the investigator for other reason
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of sleep measured by electroencephalograph
- Secondary Outcome Measures
Name Time Method