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Intervention study to develop a technique to detect reversible brain fatigue (electronic screen syndrome) by electronic screen using EEG measurement

Not Applicable
Conditions
healthy volunteers
Registration Number
JPRN-UMIN000053781
Lead Sponsor
Rohto Pharmaceutical Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
33
Inclusion Criteria

Not provided

Exclusion Criteria

1) Those who have changed or newly started using health food habitually taken within the past 4 weeks 2) Those who work night shift or day and night shift system 3) Those who are undergoing treatment (hormone replacement therapy, drug therapy, exercise therapy, diet therapy, etc.) at medical institutions for the treatment or prevention of disease, or those who are judged to be in need of treatment. 4) Subjects with a history of diagnosis of serious diseases of glucose metabolism, lipid metabolism, liver function, renal function, heart, circulatory system, respiratory system, endocrine system, immune system nervous system, or mental disease. 5) Those who have a history of alcohol dependence or drug dependence 6) Those who are pregnant, breastfeeding, or wish to become pregnant while participating in the study 7) Participated in other human studies (human studies using foods, drugs, quasi-drugs, medical devices, etc.) within the past 4 weeks, or other studies during the scheduled period of this study plan to participate in a human trial

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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