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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | HLNatural Tension | Understand 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.