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Clinical trial on psychological effect by intake of test beverage - A placebo-controlled, single-blind, crossover study -

Clinical trial on psychological effect by intake of test beverage - A placebo-controlled, single-blind, crossover study - - Clinical trial on psychological effect by intake of test beverage

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000057083
Enrollment
60
Registered
2026-03-11
Start date
2025-03-12
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 adults

Interventions

Sponsors

IMEQRD Co. Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Age: 20 or elder, and less than 35 years 2.Japanese males and females 3.BMI less than 30.0 kg/m^2 4.non-smokers (no history of smoking in the past year) 5. Individuals who have received adequate explanation regarding the trial, can comprehend its contents, and have produced written consent

Exclusion criteria

Exclusion criteria: 1.Currently undergoing medical, pharmacological, or herbal treatment (except for on-demand medicines) 2.Have a history of, or currently have serious cardiac, hepatic, renal, gastrointestinal disease 3.Have a pollen allergy or (seasonal / perennial) allergic rhinitis appeared to cause the symptoms occurrence in the test period 4.Currently receiving diet therapy or physiotherapy under medical supervision 5.Regularly taking commercially available pharmaceuticals, quasi drugs, foods for specified health use (FOSHU), foods with function claims or health food that affect autonomic nervous system, metabolism or sleep, and unable to stop taking during the test period 6. Have any difficulty in measurement using heart rate monitor (e.g. thick body hair on the chest hair, with an implanted pacemaker, etc.) 7. Have sensitive skin around electrode attachment site (chest) 8. Habitual heavy drinkers (daily pure alcohol consumption exceeding 40g) 9. Have significant inconsistency in timing of meals from day to day, or have an irregular sleep cycle (e.g. shift-workers / night shift worker) 10. Participants in other clinical trials currently or within one month before agreeing to participate in this study, or planning to participate in other clinical trials during or within 4 weeks after the test period of this study 11. May have significant stress due to life events such as relocation, job change or separation from close relatives with in 3 months before consent for this study, or planned to have such life events during this study 12. Have difficulty in abstaining from alcohol from the day before the date when study is conducted 13. Have food or drug allergy 14. frequent urination 15. Currently pregnant or breastfeeding, or hoping to get pregnant during the test period 16. Deemed unsuitable for this study by the principal investigator

Design outcomes

Primary

MeasureTime frame
Questionnaires to assess psychological state

Secondary

MeasureTime frame
Heart rate

Countries

Japan

Contacts

Public ContactHirokuni Kayama

IMEQRD Co., Ltd. Planning and Sales Department

clinical-trial@imeqrd.co.jp03-6704-5968

Outcome results

None listed

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