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Effect of taking foods with Enoki mushrooms (Flammulina velutipes) on mental and physical health in adult women

Effect of taking foods with Enoki mushrooms (Flammulina velutipes) on mental and physical health in adult women - The effect test of foods with Enoki mushrooms

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000046734
Enrollment
30
Registered
2023-03-16
Start date
2022-01-28
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 adult women

Interventions

To take 30 g of the food with Enoki mushrooms / day for 4 weeks To take 30 g of the placebo food / day for 4 weeks

Sponsors

Graduate School of Kyushu University Faculty of Agriculture
Lead Sponsor
Faculty of Humanity-Oriented Science and Engineering, Kindai University
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) Persons who are generally judged as healthy (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 demonstrate the same or similar efficacy as 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 are under treatment or determined to require medical treatment as at obtaining 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, the nervous system or mental illness (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 within the past four weeks. (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
Evaluation of skin condition by measuring instruments

Secondary

MeasureTime frame
Visual Analog scale of skin condition Stool Form Scale Profile of Mood States 2nd Edition

Countries

Japan

Contacts

Public ContactKuniyoshi Shimizu

Graduate School of Kyushu University Faculty of Agriculture Department of Agro-Environmental Sciences Laboratory of Systematic Forest and Forest Products Scien

shimizu@agr.kyushu-u.ac.jp092-802-4673

Outcome results

None listed

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