MyVitalC for sleep problems and everyday headaches
A Real-World, Single-Arm Observational Study Evaluating the Effects of MyVitalC (ESS60 in Extra Virgin Olive Oil) on Sleep Disturbance and Everyday Headaches
This program will test whether taking the MyVitalC supplement daily helps adults with sleep disturbance and routine headaches sleep better and have fewer or less severe headaches.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Sex | All |
| Sponsor | Efforia, Inc Industry-sponsored |
| Locations | 1 site (New York, New York) |
| Trial ID | NCT07477236 on ClinicalTrials.gov |
What this trial studies
This is a single-arm, real-world observational design where each participant serves as their own control. Participants complete a four-week baseline period with weekly self-reports, then take daily MyVitalC for six weeks while continuing weekly assessments. Validated patient-reported outcome measures (PROMIS Sleep Disturbance and PROMIS Pain Interference) and a custom Weekly Headache Check-In are used to measure changes. The focus is on detecting within-person signals of change rather than providing randomized controlled evidence of efficacy.
Who should consider this trial
Good fit: Adults who can consent, have sleep disturbance and routine (non-chronic) headaches, can purchase and take the supplement daily, and are willing to complete weekly assessments and daily logs are ideal candidates.
Not a fit: People with severe or chronic headache disorders, known allergies to olive oil or product components, pregnancy or breastfeeding, significant gastrointestinal conditions, or other medical issues that could be worsened by supplements are unlikely to benefit and should not participate.
Why it matters
Potential benefit: If successful, using MyVitalC could improve sleep quality and reduce the frequency or severity of everyday headaches for some people.
How similar studies have performed: Human data are limited and mostly anecdotal, so there is little robust prior evidence showing success with this specific supplement for sleep or everyday headache management.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults of legal age of consent * Able to provide informed consent * Willing to complete weekly assessments and daily logs * Able to purchase and use the study product Exclusion Criteria: * Have known allergies to olive oil or product components * Are pregnant or breastfeeding * Have severe or chronic headache disorders * Have significant gastrointestinal conditions * Have medical conditions that could be exacerbated by supplement use * Have concerns about dizziness, fatigue, or mood disturbances * Are subject to organizational or legal restrictions on supplement use
Where this trial is running
New York, New York
- Efforia — New York, New York, United States (Recruiting)
Study contacts
- Study coordinator: Matthew Amsden
- Email: help@efforia.com
- Phone: (646) 679-2479
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.