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Verification of the effects of test food on cognitive functio

Not Applicable
Conditions
Healthy adults
Registration Number
JPRN-UMIN000054058
Lead Sponsor
Miura Clinic, Medical Corporation Kanonkai
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
60
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Subjects with Alzheimer's disease (2) Subjects with a history of stroke, subarachnoid hemorrhage, cerebral infarction, cerebral hemorrhage, cerebral contusion, or head injury (3) Subjects with a history of diabetes, liver diseases, renal disease, gastrointestinal disease, cardiac disease, respiratory disease, peripheral vascular disease, or other serious disease. (4) Subjects who have undergone gastrointestinal surgery (5) Subjects with abnormal liver and renal function test value (6) Subjects with diseases currently being treated (7) Subjects who are allergic to food and drugs (8) Subjects with anemia symptoms (9) Subjects with color discrimination difficulties (10) Subjects who have difficulty performing cognitive function tests due to low visual acuity, or who have been diagnosed with low vision or blindness (11) Subjects who have depression or have been diagnosed with depression (12) Subjects with motor, visual or hearing impairments (13) Subjects who play intense sports and subjects who are on a diet (14) Subjects who work at night or have other irregularities in their daily life during the examination period (15) Subjects who cannot stop taking health foods (including foods for specified health use and foods with functional claims) and quasi-drugs during the test period (16) Subjects who are continuously treated with pharmaceuticals (including OTC and prescription drugs) (17) Subjects who drink more than 20 g of average daily pure alcohol (18) Subjects who are participating in or will participate in other clinical trials at the start of this study. (19) Other subjects judged by the investigator or the investigator to be inappropriate for the examination

Study & Design

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