MyVitalC for Sleep and Everyday Headache Management

This study is looking at whether a dietary supplement called MyVitalC (ESS60 in extra virgin olive oil) can help with sleep problems and everyday headaches. Many people experience sleep issues and headaches, and while some have reported benefits from MyVitalC, there isn't much scientific data yet. This study will help participants see if MyVitalC makes a difference in their own sleep and headache patterns. You would first track your sleep and headaches for four weeks without the supplement, and then take MyVitalC daily for six weeks, continuing to track your symptoms. The study aims to see if MyVitalC is linked to changes in how often you have headaches, how severe they are, and how well you sleep. About 100 adults are expected to join. The current status of the study is unclear.

Study design
This is a single-arm observational study, meaning all participants will receive the intervention, and it's designed to see changes within each person. It is not a randomized controlled trial.
What's involved
You would complete weekly assessments and daily logs for a total of 10 weeks (four weeks without the supplement, then six weeks taking it). You also need to buy and use the study product.
Compensation
Not stated in the trial record.
Follow-up
You will be followed for the duration of the intervention period, with a final assessment on day 70 (after the six weeks of taking MyVitalC).

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NCT07477236

MyVitalC: Sleep and Everyday Headache Management

Recruiting
NAAll AgesInterventionalHealth services
Efforia, Inc
~100 participants
Updated 2026-03-17 on ClinicalTrials.gov
What's tested:MyVitalC (ESS60 in Extra Virgin Olive Oil)

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change in Sleep Disturbance
Measured over Weekly during baseline (4 weeks) and weekly during intervention (6 weeks)
+2 more outcomes measured
Sleep
Headaches
1 sites across 1 states
New York1

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Eligibility criteria

Inclusion

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

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
  • Change in Sleep DisturbanceWeekly during baseline (4 weeks) and weekly during intervention (6 weeks)

    Measure: PROMIS Sleep Disturbance Scale Description: Assesses perceived sleep quality, sleep depth, and sleep-related difficulties. Higher scores indicate greater sleep disturbance.

  • Change in Headache FrequencyWeekly during baseline and intervention, and on day 70 (end of study)

    Measure: Weekly Headache Check-In (frequency count) Description: Number of headaches experienced in the past 7 days.

  • Change in Headache SeverityWeekly during baseline and intervention, and on day 70 (end of study)

    Measure: Weekly Headache Check-In (severity rating) Description: Participant-reported severity of the worst headache experienced during the past 7 days.