Clinical Trials Directory

Trials / Completed

CompletedNCT04091555

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

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
117 (actual)
Sponsor
Hawthorne Effect Inc. · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTHLNatural TensionUnderstand the impact of the supplement on Tension Headaches

Timeline

Start date
2019-10-16
Primary completion
2020-08-16
Completion
2020-09-16
First posted
2019-09-17
Last updated
2021-11-15

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04091555. Inclusion in this directory is not an endorsement.