JPRN-UMIN000048898已完成Unknown
A study for evaluating effects of a single intake of the test food on EEG and autonomic nervous system. - A study for evaluating effects of a single intake of the test food on EEG and autonomic nervous system.
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 入组人数
- 24
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 35years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •[1] Individuals using medical products. [2] Individuals who use a drug and Chinese traditional medicine. [3] Individuals who receive a diet remedy and an exercise therapy under medical supervision. [4] Individuals who are patient or have a history of psychiatric disease, high blood pressure, diabetes, and hyperlipidemia. [5] Individuals who have a history of serious hepatopathy, kidney damage, heart disease and hematological disease. [6] Individuals who are a patient or have a history of or endocrine disease. [7] Individuals who use implantable medical devices such as a pacemaker. [8] Individuals who used a drug to treat a disease in the past 1 month. [9] Individuals who use regularly over-the-counter medicines, quasi-drugs, food for specified health uses, functional foods, health foods and other products that affect the autonomic nervous system, metabolism and sleep. [10] Individuals who with a history of brain or heart surgery [11] Individuals who will develop seasonal allergy symptoms like hay fever or have allergic rhinitis during the test period. [12] Individuals who are or may be allergic to medical products or foods. [13] Individuals who have allergies to tape or other problems with EEG and heart rate monitor attachment. [14] Individuals who excessively take alcohol (expressed in an amount of alcohol: over 60g/day). [15] Individuals whose diet is extremely irregular. [16] Individuals whose daily life rhythm is irregular for reasons such as shift work or late nights. [17] Individuals who have experienced significant stress due to life events within 3 months prior to obtaining informed consent. [18] Individuals who are participating with other clinical trial. [19] Individuals who cannot stop drinking from the day before the test. [20] Individuals who are or are possibly pregnant, or are lactating. [21] Individuals who have severe menstrual complaints and require medication. [22] Individuals judged inappropriate for the study by the principal.
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