Evaluation of the effect of a single intake of protein hydrolysate on stress-related index
- Conditions
- Healthy adult male and female
- Registration Number
- JPRN-UMIN000049730
- Lead Sponsor
- IMEQRD Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 48
Not provided
Participants have a disease that mental and physical disorders. Participants have been diagnosed with a cognitive processing disorder. Participants have undergone gastrointestinal surgery (excluding appendicitis). Participants are currently taking over-the-counter drugs, foods for specified health uses, supplements, etc, or who cannot stop taking supplements during the study period. Participants take food for specified health use, energy drinks, etc, that aim to have effects on the autonomic nervous system, etc. Participants drink a lot of alcohol. Participants have a smoking habit (Participants less than one year after quitting smoking). Participants with irregular life rhythms (shift work, etc.). Participants may change their lifestyle during the examination period. Participants have a life event that affects their mind and body within the past month. Participants participated in a study involving the use of other foods or drugs, or the application of cosmetics or drugs within one month before obtaining consent, or who will participate in another study while participating in this study. Participants consume a large amount of dairy products, etc, every day. Participants have a habit of doing strenuous exercise at least 3-4 times a week. Participants have experienced poor mood or deterioration of physical condition due to blood collection. Participants are currently undergoing regular hospital visits and treatment for any illness. Participants have severe diseases in the liver, heart, metabolic system, etc. Participants have a history of treatment for heart failure, etc. Participants may exhibit allergy symptoms to milk or soy, or have a lactose intolerant constitution. Participants with current or past drug or food allergies. Participants are currently pregnant or breastfeeding, and who wish to become pregnant during the study period. Others subjects are judged to be inappropriate as research subjects by the principal investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method