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Dietary Intervention for Migraine Relief
Diet-Based Treatment for Migraine Relief
Who can join
Ages 18 to 75 · All sexes
Full eligibility criteria
Inclusion Criteria: * Men and women of all races and ethnicities * Age 18-75 years * Documented diagnosis of chronic or episodic migraine for at least 6 months, based on International Classification of Headache Disorders, 3rd edition (ICHD-III) criteria, defined as: * 8 headache days per month, and * 4 migraine days per month * Migraine onset before age 50 * On a stable medication regimen for at least 1 month prior to enrollment * Willing to maintain stable medications throughout the study * Willing to discontinue supplements during the study period * Women of childbearing potential must be willing to use birth control during the study timeframe Exclusion Criteria: * Current pregnancy, plans to become pregnant during the study timeframe, or current breastfeeding * Current use of medications affecting glutamatergic or gamma-Aminobutyric Acid (GABA) neurotransmission (unless discontinued under physician guidance) * Current use of quarterly injectable migraine preventive medications * Unwillingness to modify dietary intake or to stop alcohol and marijuana use during the study * Substance use disorder within the past year * Diagnosed seizure disorder * Severe asthma requiring past hospitalization
About the study
The goal of this clinical trial is to evaluate whether a low-glutamate diet can improve migraine symptoms in adults with migraine and to explore possible biological changes associated with dietary improvement. The study focuses on whether reducing dietary glutamate intake may influence processes involved in migraine, such as brain excitation, inflammation, and oxidative stress.
The main questions this study aims to answer are:
Does following a low-glutamate diet reduce the number of migraine days and the severity and duration of migraine attacks, and improve quality of life?
Are improvements in migraine symptoms associated with changes in blood-based biological markers related to migraine activity?
Researchers will compare participants assigned to the low-glutamate diet with participants assigned to a wait-list control group to evaluate differences in migraine outcomes and related biological measures.
Participants will:
Complete a baseline run-in period while tracking headaches using a daily migraine diary
Either follow a low-glutamate dietary intervention or continue their usual diet as part of a wait-list control
Complete standardized questionnaires related to migraine symptoms and quality of life
Provide blood samples for laboratory analyses
Undergo neuroimaging assessments (for a subset of participants)
What is being tested
- Dietary training (behavioral)
Sponsor: American University · Participants: 40 · Started: Mar 2, 2026
Contact the study team
- Kathleen Holton · Phone: 5037571578
Official record on ClinicalTrials.gov — NCT07360405
Locations in the U.S.
| District of Columbia | American University, Washington D.C. |
Conditions
From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.