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Clinical Trials/JPRN-UMIN000048599
JPRN-UMIN000048599
Not yet recruiting
未知

A study to evaluate the effects of the test food on improving fatigue sensation, sleep quality and cognitive function - A study to evaluate the effects of the test food on improving fatigue sensation, sleep quality and cognitive function

Japan Preventive Medicine Inc.0 sites24 target enrollmentAugust 5, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy volunteers
Sponsor
Japan Preventive Medicine Inc.
Enrollment
24
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 5, 2022
End Date
December 31, 2022
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Japan Preventive Medicine Inc.

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\)Subjects receiving a medical treatment for serious cardio\-vascular, hepatic, renal, respiratory, endocrine or metabolic disorders or having a medical history of these disorders 2\)Subjects with chronic fatigue syndrome (CFS) , or subjects deemed to have severe fatigue such as idiopathic chronic fatigue by the investigator 3\)Subjects who take regularly medicines and quasi\-drugs having the effects on fatigue sensation, sleep quality and cognitive function 4\)Subjects who take regularly Food with Functional Claims having the effects on fatigue sensation, sleep quality and cognitive function 5\)Subjects whose lifestyles are irregular because of night shift or others 6\)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) 7\)Subjects who have the possibility of developing allergic symptoms by the test food 8\)Subjects who are pregnant or lactating, or intending to become pregnant during the study 9\)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 10\)Subjects deemed unsuitable by the investigator

Outcomes

Primary Outcomes

Not specified

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