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Study of the effects of beverage containing plant ingredient on mental stress.

Not Applicable
Conditions
o (subjects with high sensitivity for mental stress)
Registration Number
JPRN-UMIN000020970
Lead Sponsor
TES Holdings Co., Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
50
Inclusion Criteria

Not provided

Exclusion Criteria

Individuals who are under treatment of some disease or who always use drug or quasi-drug other than disease treatment purposes Individuals who are or are under treatment or have a history of serious disease or/and thyroid gland disease, adrenal gland disease and/or metabolic disorder Individuals who are under treatment related to psychological stress or/and who are using related pharmaceutical products, supplements, health food Individuals who are taking anti- histamine drugs Individuals who are xerostomia or have subjective symptom of xerostomia Individuals who have under treatment or a history of drug addiction and/or alcoholism Systolic and diastolic blood pressures are over 160 mmHg and 100 mmHg, respectively Individuals who have drug allergy, food allergy and/or possibility of allergy symptoms onset Individuals who have subjective symptoms of anemia Individuals who will have or had life events which effect on mental conditions Individuals who have never used computer Individuals whose first language is not Japanese Individuals who have color blindness Individuals who are smoker Individuals who can not stop drinking alcohol during the day before and end of each test of each inspection day Individuals who can not stop to intake caffeine containing foods or beverages from morning until the end of test in each inspection day Individuals who can not have night sleep because of shift work or other reasons Workers who have holiday between weekdays Individuals who do not wake up between AM 6:00 and AM 9:00 Individuals who and whose family is engaged in healthy or functional foods Individuals who will participate in other clinical study during this study periods Individuals who will become pregnant during the current study or are pregnant or lactating Individuals who have significantly deviated value of body measurement Individuals who are judged as unsuitable for the study by the background investigation 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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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