JPRN-UMIN000039248
Completed
N/A
A clinical study to evaluate the effects of the test food on improving quality of sleep. - A clinical study to evaluate the effects of the test food on improving quality of sleep.
Japan Preventive Medicine Inc.0 sites36 target enrollmentMay 23, 2021
ConditionsHealthy volunteers
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Healthy volunteers
- Sponsor
- Japan Preventive Medicine Inc.
- Enrollment
- 36
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •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
Outcomes
Primary Outcomes
Not specified
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