1 |
Participants who were under treatment or have a history of malignancy, heart failure, myocardial infarction, psychiatric disorders, immunocompromised participants, short bowel syndrome, ulcerative colitis, valvular heart disease, or bowel obstruction |
2 |
Participants with implanted pacemakers or implantable defibrillators |
3 |
Participants who were under treatment or had experienced chronic diseases (e.g., arrhythmia, hepatopathy, nephropathy, cerebrovascular disorder, rheumatism, diabetes, dyslipidemia, hypertension) |
4 |
Participants who consume foods with possible functional properties on a regular basis |
5 |
Participants who regularly use medicines (including herbal medicines) or supplements |
6 |
Participants with allergies (to medicines and food related to the tested food) |
7 |
Participants who are pregnant, lactating, or intend to become pregnant during the study period |
8 |
Participants who have participated or will participate in other clinical trials during the 28 days prior to the date of consent form acquisition |
9 |
Participants with irregular sleeping hours and sleeping habits due to night shifts, etc. |
10 |
Participants who smoke |
11 |
Participants with infant children |
12 |
Participants who were judged as unsuitable for other reasons by the supervising physician |