MyVitalC for sleep problems and everyday headaches

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

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 it's running

• Efforia
  New York, New York, United States Recruiting

Study contacts

• Study coordinator: Matthew Amsden
• Email: help@efforia.com
• Phone: (646) 679-2479

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.