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Verification of the Effects of C132 Supplements on Cognitive Function in the Elderly

C132 Verification of the Effects of Supplement Intake on Cognitive Function in Older Adults: A Randomized Intergroup Parallel Trial - C132 supplement trial: randomized intergroup parallel trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000047685
Enrollment
40
Registered
2023-07-30
Start date
2022-05-10
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

C132 supplements a package/day for 6 weeks Placebo supplements a package/day for 6 weeks

Sponsors

Faculty of Humanity-Oriented Science and Engineering, Kindai University
Lead Sponsor
Laboratory of Systematic Forest and Forest Products Science Faculty of Agriculture, Kyushu University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Person who is over 60 years of age (2) Persons who can give voluntary Written consent to participate In the present trial

Exclusion criteria

Exclusion criteria: (1) persons who have any dietary supplements, quasi drugs or medicines which cause same or similar efficacy with the effect evaluated in this study (2) persons who have changed their habitats to take supplements within past 4 weeks. (3) Persons who work in night shift or in day and night shift (4) persons who have been treated their illness or prevention in a clinic at their informed consent (5) persons with their medical histories as follows: serious diseases of sugar metabolism, lipid metabolism, hepatic function, renal function, heart, circulatory, respiratory, endocrine system, immune system, or mental illness of the nervous system (6) persons with the medical histories of alcoholism or drug dependence (7) persons who might be developed allergic reaction to foods. (8) Persons who are pregnant, breast-feeding, or hope to be pregnant during the study period (9) persons who had always participated in or will participate in any other clinical trial (to use foods/medicine/quasi medicine/medical device) (10)persons who will not be judged suitable to the participants by the investigator.

Design outcomes

Primary

MeasureTime frame
Cognitive function test

Countries

Japan

Contacts

Public ContactKeiko Ohnuki

Faculty of Humanity-Oriented Science and Engineering, Kindai University Research and Development Department

userlifesciense@gmail.com0948-82-3123

Outcome results

None listed

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