MyVitalC for Sleep and Headaches

Overseen By Matthew Amsden

Age: Any Age

Sex: Any

Trial Phase: Academic

Sponsor: Efforia, Inc

Disqualifiers: Pregnancy, Severe headaches, Gastrointestinal conditions, others

No Placebo Group All trial participants will receive the active study treatment (no placebo)

Compensation: Varies

Number of Visits: 11

Duration: 6 weeks

100 Participants Needed

What You Need to Know Before You Apply

What is the purpose of this trial?

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.

Are You a Good Fit for This Trial?

Inclusion Criteria

I am an adult and legally able to give consent.

Able to provide informed consent

Willing to complete weekly assessments and daily logs

Exclusion Criteria

Pregnant or breastfeeding

I have serious digestive or stomach problems.

Known allergies to olive oil or product components

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Baseline Observation

Participants complete a four-week baseline observation period without the intervention, with weekly self-reported assessments

4 weeks

4 visits (virtual)

Treatment

Participants use MyVitalC daily for six weeks with weekly self-reported assessments

6 weeks

6 visits (virtual)

Follow-up

Participants are monitored for changes in sleep disturbance and headache frequency or severity after treatment

2 weeks

1 visit (virtual)

What Are the Treatments Tested in This Trial?

Interventions

• MyVitalC (ESS60 in Extra Virgin Olive Oil)

How Is the Trial Designed?

Group I: Single Arm longitudinal where participants act as their own control Experimental Treatment 1 Intervention

Single Arm longitudinal where participants act as their own control

Who Is Running the Clinical Trial?

Efforia, Inc

Lead Sponsor

Trials

3

Recruited

1,200+