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Radicle Energy VBMTM: A Study Assessing the Impact of Health and Wellness Products on Fatigue and Related Health Outcomes

2026年6月12日 更新者:Radicle Science

Radicle Energy VBMTM: A Randomized, Double-Blind, Placebo-Controlled Study Assessing the Impact of Health and Wellness Products on Fatigue and Related Health Outcomes

Radicle Energy VBMTM: A randomized, double-blind, placebo- controlled direct-to-consumer study assessing the impact of health and wellness products on fatigue and related health outcomes.

研究概览

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

介入性

注册 (估计的)

550

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

是的

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

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

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
实验性的:Active Energy Product 1
Energy Active Product 1
参与者将按照指示使用其能源活性产品1,为期6周。
安慰剂比较:Placebo Energy Control
Energy Product Placebo Control
Participants will use their Energy Product Placebo Control as directed for a period of 6 weeks.

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
疲劳的变化
大体时间:7周
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
7周

次要结果测量

结果测量
措施说明
大体时间
认知功能的变化
大体时间:7周
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
7周
睡眠的改变
大体时间:7周
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)
7周
Change in Global Mental Health
大体时间:7 weeks
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)
7 weeks

其他结果措施

结果测量
措施说明
大体时间
睡眠的最小临床重要差异 (MCID)
大体时间:7周
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)
7周
认知功能的最小临床重要差异(MCID)
大体时间:7周
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
7周
疲劳的最小临床重要差异 (MCID)
大体时间:7周
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)
7周
Minimal clinically important difference (MCID) in Global Mental Health
大体时间:7 weeks
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)
7 weeks
Change in Cognitive Abilities
大体时间:7 weeks
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)
7 weeks
Minimal clinically important difference (MCID) in Cognitive Abilities
大体时间:7 weeks
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)
7 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Susan Hewlings、Radicle Science

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

有用的网址

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月25日

初级完成 (估计的)

2027年6月25日

研究完成 (估计的)

2027年6月25日

研究注册日期

首次提交

2026年6月12日

首先提交符合 QC 标准的

2026年6月12日

首次发布 (实际的)

2026年6月17日

研究记录更新

最后更新发布 (实际的)

2026年6月17日

上次提交的符合 QC 标准的更新

2026年6月12日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Data will not be shared with researchers outside of Radicle Collaborators on this study.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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