A clinical study to evaluate the effects of the test food on improving quality of sleep.
- Conditions
- Healthy volunteers
- Registration Number
- JPRN-UMIN000039248
- Lead Sponsor
- Japan Preventive Medicine Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 36
Not provided
1) Subjects receiving a medical treatment for sleep disorders 2) Subjects receiving a medical treatment for serious cardio-vascular, hepatic, renal, respiratory, endocrine or metabolic disorders or having a medical history of these disorders 3) Subjects receiving a medical treatment for chronic diseases such as diabetes, hypertension and dyslipidemia 4) Subjects who take regularly pharmaceuticals, quasi-drugs, supplements or health foods which have an influence on study 5) Subjects who have the possibility of developing allergic symptoms by the test food 6) Subjects who live with their infants less than 1 year old 7) Subjects who sleep with others in a bedroom 8) Subjects whose lifestyles are irregular because of night shift or others 9) Subjects who wake up for urination 2 times or more during nocturnal sleep 10) Subjects who drink a lot (Subjects whose pure alcohol intake per day is 60 g or more) 11) Subjects whose body mass index (BMI) is 25 kg/m2 or more 12) Subjects having blood sample of 200 ml or more taken within 1 month, or 400 ml or more within 3 months prior to the start of the present study (e.g. donated blood) 13) Subjects who took part in another clinical study within 3 months prior to the start of the present study or who is currently taking part in another clinical study 14) Female subjects who are pregnant or lactating, or intending to become pregnant during the study 15) Subjects deemed unsuitable by the investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method