JPRN-UMIN000047467已完成未知
Effect of Daily Ingestion of Test Food on Stress Relief: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study - Effect of Daily Ingestion of Test Food on Stress Relief
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 80
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 60years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1.Subjects with a clinical history of gastrointestinal cancer or currently under treatment or anti-tumor medication. 2.Subjects with gastrointestinal disorders. 3.Subjects who may cause some skin troubles by measuring heart rate variability. 4.Subjects who take digoxin. 5.Subjects who have used antibiotics within 12 wks prior to this study. 6.Subjects who are under physician's advice, treatment, and/or medication for schizophrenia, depression, mania, neurological disorders, and/or sleep disorders. 7.Subjects with ACP. 8.Subjects with serious cerebrovascular, cardiac, hepatic, renal, gastrointestinal diseases, and/or affected with infectious diseases requiring reports to the authorities. 9.Subjects with major surgical history relevant to the digestive system. 10.Subjects with unusually high and/or low blood pressure and/or abnormal hematological data. 11.Subjects with severe anemia. 12.Pre- or post-menopausal women complaining of obvious physical changes. 13.Subjects who are at risk of having allergic reactions to drugs or foods especially based on wheat, milk, and egg. 14.Subjects who regularly take drugs and/or functional foods which affect bowel movements, gut microbiota, stress and/or sleep. 15.Subjects who regularly take staple food with high dietary fiber. 16.Subjects who regularly take yoghurt, lactic acid bacteria beverage, and/or natto. 17.Heavy smokers, alcohol addicts or subjects with disordered lifestyle. 18.Subjects who donated either 400 ml whole blood within 16 wks (women), 12 wks (men), 200 ml whole blood within 4 wks, or blood components within 2 wks, prior to this study. 19.Pregnant or lactating women or women who expect to be pregnant during this study. 20.Subjects who currently participate in other clinical trials, or participated within the last 4 wks prior to this study. 21.Any other medical and/or health reasons unfavorable to participation in this study, as judged by the principal investigator.
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