None (Healthy adults)
Conditions
Interventions
Six tablets containing test food per day for 6 weeks
Six tablets containing placebo per day for 6 weeks
Sponsors
CROee.INC
Keio University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Men and women who aware of the forgetfulness between the ages of 45 and 64, when giving the informed consent. 2) Subjects whose primary language is Japanese 3) Subjects who are diagnosed as health at pre-inspection 4) Individuals giving the written informed consen
Exclusion criteria
Exclusion criteria: 1.Subjects or their family having anamnesis of epilepsy 2.Subjects who have anamnesis of cranial nerve disease 3.Subjects who have depressive symptoms or who have been to diagnosed as depressive disorders 4.Subjects who have the history of head surgery or foreign metal in their head 5.Subjects who are being treated with hormone or who have been diagnosed as climacterium 6.Subjects who have anamnesis of heart disease or have heart pacemakers 7.Subjects who have anamnesis of febrile seizures 8.Subjects who have claustrophobia, tinnitus, asthma, or hay fever 9.Subjects who have difficulties in recognition of colors 10.Subjects whose visual or hearing acuity is too low to perform tests, or who have been diagnosed as amblyopia, blindness, or deafness 11.Subjects who may have physical deconditioning due to test foods 12.Subjects who have diseases requiring regular administration, or who have anamnesis of severe diseases 13.Subjects who are being treated for cognitive functions, or who regularly take drugs or health foods which may affect cognitive functions more than once a week 14.Subjects who regularly take foods similar to test foods or energy drinks more than once a week 15.Subjects who are, or are planning to be pregnant or nursing during study 16.Subjects who sometimes have irregular lifestyles during study 17.Heavy drinkers 18.Smokers or subjects who started smoking cessation within 12 months 19.Subjects who have taken the similar cognitive function tests within 12 months 20.Subjects who have done blood transfusion or blood donation within 3 months 21.Subjects who have participated in other clinical studies within 1 month, or who are planning to participate in other clinical studies during this study 22.Subjects who are suspected of dementia. 23.Subjects who are judged as unsuitable due to lifestyle questionnaire 24.Subjects who and whose family work in a company developing functional foods 25Subjects who are judged as unsuitable by doctor for other reasons
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| EEG measurement | — |
Secondary
| Measure | Time frame |
|---|---|
| Tests for cognitive functions Questionnaires Biochemical examination in blood Saliva Test | — |
Countries
Japan
Contacts
Public ContactShigeru Imai
CROee.INC Evidence Division
Outcome results
None listed