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Investigation for the anti-fatigue effects of a long-term ingestion of drinks in workers.

Investigation for the anti-fatigue effects of a long-term ingestion of drinks in workers. - Anti-fatigue effects of a long-term ingestion of drinks.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000036709
Enrollment
60
Registered
2021-03-31
Start date
2019-06-08
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 person

Interventions

Ingestion of test drink for 4 weeks. / Washout period for 4 weeks. / Ingestion of placebo drink for 4 weeks. Ingestion of placebo drink for 4 weeks. / Washout period for 4 weeks. / Ingestion of test d

Sponsors

RIKEN
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Healthy persons who are aged from 20 to 49 years. 2.Persons who are full-time worker on the day shift. 3.Persons who can give written informed consents.

Exclusion criteria

Exclusion criteria: 1.Persons who have previous history such as neurological disorder, nervous system disorder, cardiovascular disease, and other serious disease. 2.Persons who have previous history of nervous system disease such as unconsciousness, coma, convulsion, etc. 3.Persons who are in treatment. 4.Persons who usually take in health foods and supplements. 5.Persons who have food allergy. 6.Persons who have vision disorder or auditory disorder. 7.Persons who are pregnant or breastfeed. 8.Persons who can't drink soda. 9.Persons who had ever felt sick during a blood test. 10.Persons who are now participating in other clinical trials, or participated in other clinical trials within a month before obtaining his/her informed consent in this trial. 11.Persons who are judged not suitable to participate in this trial by investigators.

Design outcomes

Primary

MeasureTime frame
Changes in autonomic nerve function and cognitive function after the ingestion for 4 weeks.

Secondary

MeasureTime frame
Changes in symptoms of fatigue and subjective fatigue sensation after the ingestion for 4 weeks.

Countries

Japan

Contacts

Public ContactKei Mizuno

RIKEN Health Evaluation Team

keimizuno@riken.jp078-569-8868

Outcome results

None listed

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