JPRN-UMIN000042928已完成未知
Trial for reduction of anxiety and fatigue -open study- - Trial for reduction of anxiety and fatigue
IMEQRD inc.0 个研究点目标入组 20 人开始时间: 2022年1月13日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 20
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
- 50years-old 至 65years-old(—)
- 性别
- Female
入选标准
- 未提供
排除标准
- •Subjects who 1.are currently receiving any types of medicines and/or Chinese medical treatment (except for the drugs taken as needed). 2.plan to change their lifestyle during the test. 3.have a serious illness such as liver, kidney, heart, respiratory tract, endocrine, metabolic disease, etc.. 4.are receiving treatment for mental illness such as depression or anxiety disorder, or have a history of it. 5.May take sleeping pills/ sleep-inducing drugs during the test period, continuously or when they need. 6.Have been diagnosed with chronic fatigue syndrome. 7.Have had life events that affect their mind and body such as loss of important things within one month (death of relatives, loss of employment, divorce, pet death). 8.Take healthy foods or supplements daily. (acceptable if they can stop taking after obtaining consent.) 9.have a past and current medical history of drug or food allergy. 10.have participated in other clinical trials within one month before obtaining consent, or those who plan to participate during the trial period. 11.consume alcohol excessively (alcohol equivalent 60g or more / day). 12.have smoking habit. 13.have an irregular diet, or irregular life rhythms (work in shifts, work late at night etc.). 14.are judged by the investigator to be unsuitable for participating in this study.
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