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Anti-Fatigue Effect of NIHONSYOKU: Cross-Over Study

Anti-Fatigue Effect of NIHONSYOKU: Cross-Over Study - Anti-Fatigue Effect of NIHONSYOKU

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000021997
Enrollment
40
Registered
2016-04-20
Start date
2015-10-17
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

Interventions

Ingestion of a test meal for dinner for 2-4 weeks. Ingestion of a placebo meal for dinner for 2-4 weeks.

Sponsors

Osaka City University Center for Health Science Innovation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Healthy persons who are aged from 18 to 79 years. 2.Persons who are not shift worker.

Exclusion criteria

Exclusion criteria: 1.Persons who are in treatment. 2.Persons who have medical history of cardiovascular disease such as arrhythmia and angina pectoris, etc. 3.Persons who have autonomic nervous system dysfunction. 4.Persons who have medical history of nervous system disease such as unconsciousness, coma, and convulsion, etc. 5.Persons who have insomnia. 6.Persons who have food allergy. 7.Persons who are heavy user of alcohol. 8.Persons whose body mass index is less than 17 and more than 31. 9.Persons who are on a diet. 10.Pregnant women. 11.Persons who are judged not suitable to participate in this trial by investigators.

Design outcomes

Primary

MeasureTime frame
Subjective fatigue degree Autonomic nervous function Cognitive function Oxidation stress Antioxidant activity

Secondary

MeasureTime frame
Amount of activity Other biochemical tests

Countries

Japan

Contacts

Public ContactKei Mizuno

Osaka City University Center for Health Science Innovation

chsi-b@ado.osaka-cu.ac.jp06-6485-0288

Outcome results

None listed

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