Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
NCT07477236

MyVitalC: Sleep and Everyday Headache Management

Led by Efforia, Inc · Updated on 2026-03-17

100

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Sleep disturbance and recurring headaches can negatively affect daily functioning, mood, and productivity. MyVitalC (ESS60 in extra virgin olive oil) is a commercially available dietary supplement that has generated anecdotal claims related to sleep quality and headache relief; however, human data remain limited. This real-world observational study is designed to help participants evaluate whether use of MyVitalC is associated with changes in sleep disturbance and headache frequency or severity in their own daily lives. Participants will complete a four-week baseline observation period without the intervention, followed by six weeks of daily MyVitalC use, with weekly self-reported assessments. Participants serve as their own control, allowing for within-person comparison of outcomes before and during product use.

CONDITIONS

Official Title

MyVitalC: Sleep and Everyday Headache Management

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • Known allergies to olive oil or product components
  • Pregnant or breastfeeding
  • Severe or chronic headache disorders
  • Significant gastrointestinal conditions
  • Medical conditions that could be worsened by supplement use
  • Concerns about dizziness, fatigue, or mood disturbances
  • Subject to organizational or legal restrictions on supplement use

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Efforia

New York, New York, United States, 10003

Actively Recruiting

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Research Team

M

Matthew Amsden

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

1

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