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Effects of a 12-week functional water intake

Effects of a 12-week functional water intake on anti-fatigue and health benefits - Effects of a 12-week functional water intake on anti-fatigue and health benefits

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055148
Enrollment
80
Registered
2024-08-05
Start date
2024-09-07
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

Intake of the test drink twice a day for 12 weeks Intake of the placebo drink twice a day for 12 weeks

Sponsors

ASAHI SOFT DRINKS CO., LTD.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Individuals aged 20 to 65 years who do not meet the exclusion criteria. 2. Individuals who understand the contents of the informed consent explanation and can provide written consent voluntarily.

Exclusion criteria

Exclusion criteria: 1. Individuals with a history of serious diseases related to the brain, nervous system, cardiovascular system, or other severe conditions, or those currently undergoing treatment, including those taking prescribed medication. 2. Individuals with a history of seizures (such as loss of consciousness, coma, convulsions, etc.). 3. Individuals currently suffering from peptic ulcers (such as gastric ulcers). 4. Individuals with hearing or vision impairments that make it difficult to complete the essential evaluation items of this study. 5. Individuals who are currently pregnant or breastfeeding. 6. Individuals who cannot consume sugar-free carbonated beverages and cold drinks. 7. Individuals who have experienced symptoms of a vasovagal response due to blood sampling in the past. 8. Individuals currently participating in another clinical trial or who have participated in another interventional clinical trial within one month prior to obtaining consent. 9. Individuals who cannot comply with operational instructions for the trial (e.g., wearing masks for infection prevention). 10. Individuals deemed unsuitable by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Comparison of psychological, physiological, and biochemical parameters before and after the intake of the functional water.

Countries

Japan

Contacts

Public ContactKyosuke Watanabe

Osaka Metropolitan University Center for Health Science Innovation

kyosuke.watanabe@dragon.kobe-u.ac.jp+81-6-6485-0288

Outcome results

None listed

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