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临床试验/NCT04091555
NCT04091555已完成不适用

Evaluation of the Impact of the HL Natural, Inc. Tension Relief Product on the Reduction of Symptoms in Adults Who Suffer From Mild to Moderate Tension Headaches

Hawthorne Effect Inc.2 个研究点 分布在 1 个国家目标入组 117 人开始时间: 2019年10月16日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
117
试验地点
2
主要终点
The Evaluation of the Impact of HLNatural Tension Relief Product for Adults who Suffer from Mild to Moderate Tension Headaches

研究概览

简要总结

The primary hypothesis of the present study is that supplementation with the Tension Relief test product will reduce the severity of symptoms of a tension headache.

详细描述

Patients will begin taking the capsules at the onset of headache symptoms. Onset is defined as the point in time the participant feels that it is necessary to take the test product for relief of symptoms. When the participant decides to take the test product, they will report symptoms in the headache diary prior to taking the product and rate their symptoms on a 10-point Mankoski scale. After consuming the product, the participant will complete a Mankoski scale at 15 minutes, 30 minutes and 1 hour after taking the product. If needed the participant will be allowed to take alternative medication (alternative treatment) after an hour after taking the product. If alternative medication is taken, the participant will record this in their headache diary.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult candidates who are in overall good health and who suffer from mild to moderate tension headaches.
  • Participants will be deemed to be in good health if they do not report any of the existing medical conditions asked about in the screening questionnaire.

排除标准

  • Those who have been diagnosed with migraine headaches.
  • Those who score between 36-49 or 60-78 on screening questionnaire.
  • Is < 18 years of age
  • Those who have been diagnosed with fibromyalgia.
  • Women that are pregnant or breastfeeding.
  • Alcohol consumption more than 7 drinks per week or more than 3 drinks per occasion.
  • Routine recreational drug use such as marijuana.
  • Chronic renal disease
  • Chronic liver disease
  • Allergy to any of the following: Aspirin or any other product including Salicylates, Boswellia, Feverfew, Skullcap, White Willow Bark, Rice Hull, or Vegetable Cellulose.
  • Unable to swallow pills.
  • Unwilling to try test product for relief of pain and tension headache symptoms.
  • Participants who are currently taking any anticoagulation medications daily. (Aspirin, Warfarin, Heparin etc.)

结局指标

主要结局

The Evaluation of the Impact of HLNatural Tension Relief Product for Adults who Suffer from Mild to Moderate Tension Headaches

时间窗: After taking the test product, the participant will complete a Mankoski pain scale at 15 minutes after the start of the event, 30 minutes after the start of the event, and 1 hour after the start of the event.

Those subjects who meet the inclusion/exclusion criteria will be invited to be part of the study. The subject will sign consent and complete the required surgery and questionnaires before taking the test product. • At the onset of the headache, the participant will start a Headache Diary and complete a 10-point Mankoski pain scale. • After completing the surveys, the participant will take test product. The participant will take 2 capsules with 6-8 oz. of water per headache episode. With a max of 6 pills per day.

次要结局

  • Outcome of Subjects Natural Behavior During the Clinical Trial(10-point Mankoski Scale and Headache Diary will be at the start of the headache, 15 minutes after start of the event, 30 minutes after start of event and 60 minutes after the start of the event. The activity will be repeated for up to 3 events.)
  • Outcome of all Adverse Events while consuming HLNatural Suppliement(All adverse events will be captured throughout the 60 days or after 3 episodes of headaches or until the subject exits the trial.)
  • Understanding If HLNatural impacts the Intensity of Tension Headaches. Headaches.another intervention(Stubjects will be evaluated for up to 60 days or 3 episodes of a headache)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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