ACTRN12619001461189已完成未知
nderstanding the calming effect of passionflower in healthy people
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 91
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 45 Years(—)
- 性别
- All
入选标准
- •Healthy adults between 18 and 45 years of age will be eligible for this study. Proficiency in English will be a requirement for participants (due to the nature of outcome assessment tools).
排除标准
- •have psychiatric disorders (including psychotic or bipolar disorder illness, major depressive disorder, or any specific anxiety disorder),
- •have had either substance abuse or dependency disorder in the previous six months, including alcohol
- •are currently using antidepressants, mood stabilisers, antipsychotics, opioid, or analgesics
- •are diagnosed with known abnormal liver function and/or inflammatory diseases
- •have experienced adverse reactions to passionflower or any active ingredients of study materials
- •have regularly used passionflower in the previous 12 months
- •have had more than one occasion of passionflower use each week over the past month
- •are pregnant or trying to conceive
- •are breastfeeding
- •are regular smokers (more than one cigarette per week)
- •are unable to comply with the abstention of caffeinated products and exercise for two hours and alcohol for a minimum of 12 hours prior to visits
研究者
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