Radicle Energy VBMTM: A Study Assessing the Impact of Health and Wellness Products on Fatigue and Related Health Outcomes
Radicle Energy VBMTM: A Randomized, Double-Blind, Placebo-Controlled Study Assessing the Impact of Health and Wellness Products on Fatigue and Related Health Outcomes
研究概览
地位
详细说明
This is a randomized, double-blind, placebo-controlled study conducted with adult participants, residing in the United States. Eligible participants will (1) consume less than 3 caffeinated beverages a day, (2) have the opportunity for meaningful improvement (at least 30%) in their primary health outcome, and (3) express acceptance in taking a product and not knowing its formulation until the end of the study.
Participants that report a known contraindication or with well- established, significant safety concerns due to illness will be
excluded. Heavy drinkers and those who report they are pregnant, trying to become pregnant, or breastfeeding will be excluded. Participants that report taking medications with a known contraindication or with well-established, significant safety concerns will be excluded. Self-reported data are collected electronically from eligible participants for 7 weeks. Participant reports of health indicators will be collected at enrollment and throughout the active period of study product usage. All study assessments will be electronic; there are no in-person visits or assessments for this real-world evidence study.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Study Manager
- 电话号码:858-779-0086
- 邮箱:studymgmt@radiclescience.com
研究联系人备份
- 姓名:Susan Hewlings
- 邮箱:susan.hewlings@radiclescience.com
学习地点
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California
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Del Mar、California、美国、92014
- Radicle Science Inc.
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接触:
- Study Manager
- 电话号码:760-281-3898
- 邮箱:studymgmt@radiclescience.com
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接触:
- Megan Mosely
- 邮箱:megan@radiclescience.com
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Participants must meet all the following criteria:
Adults, at least 21 years of age at the time of electronic consent, inclusive of all ethnicities, races, and gender identities
- Assigned sex at birth will determine sex-specific recruitment and PROs (male vs female) employed, when needed
- Resides in the United States
- Has the opportunity for at least 30% improvement in their primary health outcome
- Expresses a willingness to take a study product and not know the product identity (active or placebo) until the end of the study
3.2 Exclusion
Individuals who report any of the following during screening may be excluded from participation:
- Report being pregnant, trying to become pregnant, or breastfeeding
- Unable to provide a valid US shipping address and mobile phone number
- Reports current enrollment in another clinical trial
- Reports being a heavy drinker (defined as drinking 3 or more alcoholic beverages per day)
- Unable to read and understand English at a 7th grade level
- Reports a current and/or recent (up to 3 months ago) major illness and/or surgery that poses a known, significant safety risk.
Reports a diagnosis of cardiac dysfunction, liver or kidney disease that presents a known contraindication and/or a significant safety risk with any of the study product ingredients.
- NYHA Class III or IV congestive heart failure, atrial fibrillation, uncontrolled arrhythmias, cirrhosis, end-stage liver disease, stage 3b or 4 chronic kidney disease, or kidney failure
Reports taking medications that have a well-established moderate or severe interaction, posing a substantial safety risk with any of the study product ingredients.
- Anticoagulants, antihypertensives, anxiolytics, antidepressants, chemotherapy, immunotherapy, sedative hypnotics, seizure medications, medications that warn against grapefruit consumption, corticosteroids at doses greater than 5 mg per day, diabetic medications, oral anti-infectives (antibiotics, antifungals, antivirals) to treat an acute infection, antipsychotics, MAOIs, or thyroid products
- Reports current use of caffeine-alternative products
- Reports consuming 3 or more caffeinated beverages a day
- Lack of reliable daily access to the internet
学习计划
研究是如何设计的?
设计细节
- 主要用途:其他
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Active Energy Product 1
Energy Active Product 1
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参与者将按照指示使用其能源活性产品1,为期6周。
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安慰剂比较:Placebo Energy Control
Energy Product Placebo Control
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Participants will use their Energy Product Placebo Control as directed for a period of 6 weeks.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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疲劳的变化
大体时间:7周
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疲劳变化:通过患者报告结果测量系统 (PROMIS) 疲劳 8A(8-40 级;分数越高表示疲劳越严重)评估的疲劳评分随时间变化率的差异
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7周
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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认知功能的变化
大体时间:7周
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认知功能的变化:通过 PROMIS 认知功能 8A(量表 8-40;其中较低的分数对应于较差的认知功能)评估的认知功能评分随时间变化率的差异
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7周
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睡眠的改变
大体时间:7周
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睡眠变化:通过 PROMIS 睡眠障碍 8A 评估的睡眠评分随时间变化率的差异(8-40 级;分数越高,睡眠障碍水平越高)
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7周
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Change in Global Mental Health
大体时间:7 weeks
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Change in Global Mental Health: Difference in rates of change over time in cognitive function score as assessed by PROMIS Global Mental Health 4A (scale 4-20; where lower scores correspond to worse cognitive function)
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7 weeks
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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睡眠的最小临床重要差异 (MCID)
大体时间:7周
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睡眠中的最小临床重要差异 (MCID):根据 PROMIS 睡眠障碍 8A 评估,睡眠评分出现最小临床重要差异的可能性(8-40 级;分数越高,睡眠障碍水平越高)
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7周
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认知功能的最小临床重要差异(MCID)
大体时间:7周
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认知功能的最小临床重要差异 (MCID):根据 PROMIS 认知功能 8A(量表 8-40;其中较低的分数对应于较差的认知功能)评估,认知功能评分出现最小临床重要差异的可能性
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7周
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疲劳的最小临床重要差异 (MCID)
大体时间:7周
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疲劳的最小临床重要差异 (MCID):根据 PROMIS 疲劳 8A 评估,疲劳评分出现最小临床重要差异的可能性(8-40 级;分数越高,疲劳越严重)
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7周
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Minimal clinically important difference (MCID) in Global Mental Health
大体时间:7 weeks
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Minimal clinically important difference (MCID) in Global Mental Health: Likelihood of experiencing minimal clinically important difference in cognitive function score as assessed by PROMIS Global Mental Health (scale 4-20; where lower scores correspond to worse cognitive function)
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7 weeks
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Change in Cognitive Abilities
大体时间:7 weeks
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Change in Cognitive Abilities: Difference between rates of change over time in sleep score as assessed by PROMIS Cognitive Abilities 8a (scale 8-40; where the higher scores correspond to worse sleep)
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7 weeks
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Minimal clinically important difference (MCID) in Cognitive Abilities
大体时间:7 weeks
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Minimal clinically important difference (MCID) in Cognitive Abilities: Likelihood of experiencing minimal clinically important difference in sleep score, as measured by PROMIS Cognitive Abilities (scale 8-40; where the higher scores correspond to worse sleep)
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7 weeks
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合作者和调查者
调查人员
- 首席研究员:Susan Hewlings、Radicle Science
出版物和有用的链接
有用的网址
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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