Evaluation of the Impact of the HL Natural, Inc. Tension Relief Product

Completed · Not applicable

Conditions studied: Tension, Headache

In brief

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.

Key facts

Study ID

NCT04091555

Run by

Hawthorne Effect Inc.

People needed

117

Starts

2019-10-16

Expected to finish

2020-09-16

Last updated by the study team

2021-11-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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.)

Where it is running

• Hawthorne Effect, Inc. — Lafayette, California, United States

Full record on ClinicalTrials.gov

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