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The effects of cognitive training on the intestinal environment

A study on the effects of cognitive training on the intestinal environment - A study on the effects of cognitive training on the intestinal environment

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060216
Enrollment
15
Registered
2026-01-01
Start date
2025-11-22
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 adults

Interventions

Face Name Associative Memory Exam

Sponsors

Kyodo Milk Industry Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Japanese men and women aged between 40 and 60 years. 2. Individuals who do not regularly engage in brain training; however, individuals who have not engaged in brain training for at least six months are eligible to participate. 3. Individuals who voluntarily agreed to participate in the study after receiving ufficient explanation and providing written informed consent

Exclusion criteria

Exclusion criteria: 1. Individuals who currently require medication or regular medical visits 2. Individuals undergoing dietary or exercise therapy under medical supervision. 3. Individuals with current or past history of serious diseases 4. Individuals who regularly consume over-the-counter medications, quasi-drugs, dietary supplements, or foods with health claims such as Foods for Specified Health Uses (FOSHU) or Foods with Functional Claims (FFC); however, those who are able to discontinue such use after giving consent may be eligible to participate. 5. Individuals with drug or food allergies. 6. Individuals who have donated blood components or 200 mL of whole blood within one month prior to the start of the study. 7. Individuals who have donated 400 mL of whole blood within four months prior to the start of the study. Individuals who have participated in other clinical trials or clinical studies within one month prior to obtaining informed consent, are currently participating, or plan to participate during the study period. 9. Women who are currently pregnant or breastfeeding, or who plan to become pregnant during the study period." 10. Individuals with habitual excessive alcohol consumption (>=60 grams of ethanol per day). 11. Individuals with irregular lifestyles, including those with highly irregular eating habits, shift work, or night shifts 12. Individuals with constipation or a tendency toward constipation who are deemed unable to submit stool samples for this trial 13. Individuals who regularly engage in brain training, including free or paid brain training apps, memory games, and brain training drills from books and magazines; however, individuals who have not engaged in brain training for at least six months are eligible to participate. 14. Individuals judged by the principal medical doctor to be inappropriate for participation in the study.

Design outcomes

Primary

MeasureTime frame
Fecal microbiome Fecal metabolites

Secondary

MeasureTime frame
Memory test score Fecal form (Rome Foundation's Bristol Stool Form Scale)

Countries

Japan

Contacts

Public ContactTsuyoshi Takahama

Seishukai Clinic Clinical trial office

t-takahama@seishukai.or.jp080-4410-9269

Outcome results

None listed

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