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Cocoa Extract for Migraine Trial

Cocoa Extract for Migraine Trial

Recruiting
18 years and older
All
Phase N/A

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Overview

The goal of this clinical trial is to assess the feasibility of recruitment and adherence to a high-dose cocoa extract supplement in individuals diagnosed with episodic migraine. The main questions it aims to answer are:

  • Will we be able to enroll 114 participants during the recruitment period?
  • Will participants take study pills daily during the pill-taking period?

Researchers will compare two doses of cocoa extract to placebo to determine the acceptability of higher doses of cocoa extract supplementation in this patient population.

Participants will be asked to:

  • Provide two urine samples
  • Complete daily questionnaires
  • Take four study pills a day for 12 weeks

Eligibility

Inclusion Criteria:

  • Women and men aged ≥18 years
  • Self-reported clinician diagnosis of migraine with or without aura which does not meet criteria for chronic migraine (according to the International Classification of Headache Disorders 3rd edition)
    • Individuals with self-reported migraine will need to report a clinician diagnosis of migraine and be classified as having migraine or probable migraine by the American Migraine Study (AMS) migraine screener. The AMS migraine screener, which has a sensitivity of 100% and a specificity of 82% for the diagnosis of migraine will be used to confirm self-reported migraine status.
    • History of migraine dating for at least one year
  • Self-report of 4 to 14 migraine attacks during the 30 days prior to enrollment in

    the study

  • Completion of at least 22 headache diary days during the 28 day run-in period
    • Report migraine frequency between 4 to 14 days during the 28 day run-in period
  • If currently using medications to prevent or treat migraine, no new medication use

    within the past 3 months

  • No new use of behavioral interventions within the past 3 months and/or agree to not begin new behavioral interventions during this trial
  • Be willing to complete all study procedures and be randomized to all interventional groups
  • Be fluent in English
  • Own an iPhone or Android device and be willing to download MyCap to the device

Exclusion Criteria:

  • Self-reported history of stroke or transient ischemic attack; history of brain surgery or spine surgery; currently receiving treatment for a concussion; and self-reported diagnosis of cluster headache, brain tumor, brain aneurysm, traumatic brain injury, multiple sclerosis, epilepsy, schizophrenia, or bipolar disorder
  • Kidney failure or current dialysis treatment or any medical condition which the participant believes could lead to difficulty complying with the protocol
  • Current alcohol or substance abuse (self-reported)
  • Self-reported clinician diagnosis of medication overuse headache
  • Currently or recently (past 6 months) received Botox treatment for migraine
  • Failure to return the baseline urine sample
  • Currently pregnant, nursing, or intending to become pregnant during the study period.
  • Unwilling to forgo use of out-of-study supplements of cocoa extract during the trial
  • Extreme sensitivity to caffeine

Study details
    Migraine

NCT06808230

Brigham and Women's Hospital

15 October 2025

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FAQs

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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