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A study of the effects of test food on cognitive function -A randomized, double-blind, placebo-controlled, parallel study

A study of the effects of test food on cognitive function -A randomized, double-blind, placebo-controlled, parallel study - A study of the effects on cognitive function

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000047433
Enrollment
24
Registered
2022-04-08
Start date
2022-05-15
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy subjects (including MCI) who are aware of the decline in cognitive function due to aging

Interventions

Oral intake of the test foods (3 chewable in a day for 12 weeks) Oral intake of the placebo foods (3 chewable in a day for 12 weeks)

Sponsors

Kanyukai clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Healthy subjects with MMSE results by screening test of 24 points or more(healthy person who feels deterioration of cognitive function due to aging and person with mild cognitive impairment) 2) Healthy adults aged 40 to 75 years old. 3) Gender: No preference 4) Subjects without smoking habits 5) Subjects who do not have a habit of taking a meal containing test foods (dairy products such as milk, yogurt, and cheese) 6)Subjects who do not regularly use supplements and health foods (including lactic acid bacteria and bifidobacteria) 7) Subjects who do not suffer from lifestyle diseases (high blood pressure, diabetes etc.), rheumatism, liver disorders, renal disorders, other chronic diseases 8) Subjects who have no history of treatment of malignant tumor, heart failure, myocardial infarction 9) Subjects who have no history of allergy to test foods / medicines 10) Subjects who do not take medication for Outpatient treatment 11)Subjects who are judged by the investigator to have no problem in conducting the trial based on the results of blood tests. 12) Subjects giving written informed consent

Exclusion criteria

Exclusion criteria: 1) Females who are pregnant or lactating, and females who could become pregnant or lactating during test period 2) Subjects who are participating the other clinical tests. Subjects who participated within 3-month prior to the current study 3) Subjects who do not comply with instructions from the doctor or medical staff 4) Others who have been determined ineligible by investigator

Design outcomes

Primary

MeasureTime frame
Evaluation of cognitive function by Cognitrax test at 0 week and at 12 weeks

Secondary

MeasureTime frame
Evaluation of bowel movements by Defecation survey form at 0 week and at 12 weeks

Countries

Japan

Contacts

Public ContactTaisuke Fukaya

Tashikani Plus Co., Ltd CEO

fukaya@tashikani.jp06-6352-6622

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026