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Enrolling by invitation NCT07698249

Headache Diary for Migraine Patients

No phase Interventional Migraine

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Headache diary.
Who it may be relevant to
Registry conditions: Migraine. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Use of a Headache Calendar/Journal in Patients Who Have Migraine

Overview

Use of a headache journal/calendar in patients who have migraine to ascertain if keeping a headache journal affects the quality of life and the headache burden.

Interventions

  • Behavioral Headache diary
    Completion of the virtual diary/calendar

Primary outcome measures

  • Migraine Specific Quality of Life [Time frame: Baseline, 4 weeks, 8 weeks, 12 weeks, and 24 weeks]
Secondary outcome measures (1)
  • Migraine Disability Assessment (MIDAS) score [Time frame: Baseline, 4 weeks, 8 weeks, 12 weeks, and 24 weeks]

Eligibility criteria

Inclusion criteria

  • Adults diagnosed with migraine (episodic or chronic) according to ICHD-3 criteria, with at least 3 months of confirmed diagnosis. Both episodic migraine (≤14 headache days/month) and chronic migraine (≥15 headache days/month) are eligible and will be recorded as a demographic subgroup variable.

Exclusion criteria

  • Individuals under the age of 18
  • Non-English speaking individuals

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Supportive care

Study locations

United States · 1 center
  • Hackensack Meridian Health - JFK Medical Center — Edison

Identifiers

NCT: NCT07698249 · Pro2024-0201

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗