Healthy adults
Conditions
Interventions
A single intake of 500g of Test Food A.
A single intake of 500g of Test Food B.
A single intake of 500g of Test Food C.
A single intake of 500g of Test Food D.
A single intake of 500g of Test Food E.
Sponsors
IMEQRD Co., Ltd
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Age: Over 20 and under 60 2. Gender: Japanese males and females 3. Those who can enter electronic medical questionnaires via smartphone or iPad 4. Those who voluntarily participated after receiving a full explanation of the purpose and content of the study and gave written consent to participate
Exclusion criteria
Exclusion criteria: 1. Those currently receiving treatment for any disease, or undergoing treatment with medication or Chinese medicine (intermittent use acceptable) 2. Those who experienced significant changes in lifestyle habits (diet, sleep, exercise habits, etc.) or environment (moving, unemployment, divorce, death of a spouse or relative, etc.) within a month before obtaining consent 3. Those planning to make significant changes to their lifestyle habits (diet, sleep, exercise habits, etc.) during the study period 4. Those with abnormalities in smell or taste 5. Those with diseases related to saliva secretion, such as dry mouth or Sjogren's syndrome 6. Those with drug addiction, or had in the past 7. Those with severe liver, kidney, heart, respiratory, endocrine, or metabolic diseases (diabetes), either current or past 8. Those who have undergone gastrointestinal surgery (excluding appendicitis) 9. Those with current or past drug allergies or food allergies 10. Those currently taking over-the-counter medicines and quasi-drugs, health food, or supplements for health maintenance or recovery, and cannot stop taking them during the study period 11. Those with irregular lifestyles (shift work, night work, etc.) 12. Heavy drinkers (pure alcohol intake: 40g/day or more) 13. Those currently pregnant or breastfeeding, or wishing to become pregnant during the study period 14. Those who participated or are participating in other clinical studies within a month before obtaining consent, or planning to participate during the study period 15. Those deemed unsuitable for participation in this study by the research physician.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - Hedonic VAS - Homeostatic VAS - Sensory VAS - Salivary markers | — |
Countries
Japan
Contacts
Public ContactHirokuni Kayama
IMEQRD Co., Ltd. Planning and Sales Department
Outcome results
None listed