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Exploratory study of anti-fatigue effects of tea ingestion during exercise under heat stress

Exploratory study of anti-fatigue effects of tea ingestion during exercise under heat stress - Exploratory study of anti-fatigue effects of tea ingestion during exercise under heat stress

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000061500
Enrollment
8
Registered
2026-05-11
Start date
2026-05-11
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

Interventions

Ingestion of the test beverage. Ingestion of the control beverage.

Sponsors

Osaka Metropolitan University
Lead Sponsor
Integrated Health Science Co., Ltd.
Collaborator

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Individuals who aged 20 to 39 and do not meet the exclusion criteria. 2. Individuals who understand the contents of the informed consent explanation and can provide written consent voluntarily. 3. Individuals who do not meet any of the exclusion criteria.

Exclusion criteria

Exclusion criteria: 1. Individuals with a history of serious diseases of the brain, nervous system, cardiovascular system, renal failure or other severe disorders. 2. Individuals with a history of seizures (such as loss of consciousness, coma, or convulsions) due to neurological disorders. 3. Individuals who are currently under treatment or those taking prescribed medications. 4. Individuals who have difficulty performing essential evaluation items in this study due to hearing or visual impairments. 5. Individuals with food allergies. 6. Individuals who have smoked within one year prior to obtaining informed consent. 7. Individuals who consumed an average of five or more cups of tea per day within one month prior to obtaining informed consent. 8. Individuals who consumed an average of 5 or more lemons per day, or lemon-containing foods equivalent to about 5 lemons per day within one month prior to obtaining informed consent. 9. Individuals who are currently participating in another clinical trial, or who have participated in another clinical trial within one month prior to obtaining consent. 10. Individuals who cannot follow instructions for infection prevention (e.g., wearing a mask). 11. Individuals judged as inappropriate for participation by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Changes in autonomic nervous system activity and salivary stress markers after recovery from fatigue.

Secondary

MeasureTime frame
Subjective fatigue sensation after recovery from fatigue.

Countries

Japan

Contacts

Public ContactKyosuke Watanabe

Integrated Health Science Co., Ltd. Research Division

contact@integhs.jp080-2466-6100

Outcome results

None listed

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