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Nutritinal luchbox trial at tutoring school.

Evaluation of the nutritional lunchbox on junior and senior highschool students attending private tutoring school. Cross-over test. - Evaluation of the nutritional lunchbox on junior and senior highschool students attending private tutoring school. Cross-over test.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060397
Enrollment
100
Registered
2026-01-19
Start date
2024-06-21
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

Japanese healthy junior and senior highschool students

Interventions

Functional Lunch Boxes for 4 weeks, including 140g of sticky barley-rice, 230g of functional side dish and 2g of functional tea. Regular meals daily taken for 4 weeks

Sponsors

Flowing co. ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Healthy junior and senior highschool students who attend Tokushinkan Academy. 2. Junior and senior high schoolstudents who have a personal smartphone and can prepare a google account. 3. Students who fully understand the significance, content, and purpose of this examination, and who have given their consent in writing to participate in this examination.

Exclusion criteria

Exclusion criteria: 1. Subjects who are under physicians advice, treatment, and/or medication for schizophrenia, depression, mania, neurological disorders, and/or sleep disorders. 2. Subjects with serious cerebrovascular, cardiac, hepatic, renal, gastrointestinal diseases, and/or affected with infectious diseases requiring reports to the authorities. 3. Subjects with major surgical history relevant to the digestive system such as gastrectomy, gastrorrhaphy, enterectomy, etc. 4. Subjects with implantable electronic medical devices. 5. Subjects who are under nutritional advice by a physician. 6. Subjects who cannot continue to consume the test foods due to allergic reactions to drugs or foods. 7. Subjects who regularly use medicines (sleeping pills, psychotropic drugs, etc.) or health foods/supplements (glycine, gamma-aminobutyric acid, L-serine, L-theanine, L-ornithine, reduced coenzyme Q10, etc.) that affect stress and sleep. 8. Subjects with disordered lifestyle 9. Subjects who donated blood within 4 wks, prior to the current study. 10. Pregnant or lactating women or women who expect to be pregnant during this study. 11. Subjects who currently participate in other clinical trials or participated within the last 4 wks prior to the current study. 12. Subjects who have difficulty completing a full meal of the study food due to a small appetite. 13. Any other medical and/or health reasons unfavorable to participation in the current study, as judged by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Subjective learning efficiency

Secondary

MeasureTime frame
Mental and physical complaints (fatigue, irritability, anxiety, somatic complaints) Sleep quality Mental and physical state during study Stress during study Skin condition

Countries

Japan

Contacts

Public ContactKatsuhisa Tanaka

Flowing co. ltd. Representative Director

uketuke@flow-net.jp+81-79-232-6399

Outcome results

None listed

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