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Headache Ear Auditory Dizziness Sinus (HEADS) Registry

Who can join

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
18 Years and older
Sex
All sexes
Healthy volunteers
Accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

  • Procedures mentioned: Questionnaires

Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.

Show the study's own words
  • "The study consists of a baseline questionnaire as well as annual follow-up questionnaires to follow patients prospectively and continue to collect data that meets the needs of the community."
Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

In plain language

The HEADS Registry follows U.S. adults who have sinus, balance, hearing, or headache symptoms over time. Participants answer online questions about their symptoms, how they affect daily life, and how well treatments have helped. The goal is to better understand these symptoms and improve diagnosis and treatment.

The Headache, Ear, Auditory, Dizziness, Sinus (HEADS) Registry is a study over time of individuals living in the United States who experience sinus, vestibular, auditory, and headache symptoms. Through an online portal, participants are asked questions about their symptoms, how they have affected their lives, and how effectively they have managed them. This information is then used to better understand these symptoms and to improve patient diagnosis and treatment. Some potential research benefits of the HEADS Registry include: * Improving healthcare professionals' understanding of the causes of specific head and neck symptoms. * Reducing delays in diagnosis and the use of inappropriate tests, medications, and surgeries. * Finding the most effective treatments for sinus, vestibular, and auditory disorders. * Providing participants the opportunity to be contacted for additional important research related to sinus, vestibular, and auditory disorders. All U.S. residents over the age of majority who experience sinus, vestibular, and auditory symptoms, with or without migraine, are eligible to participate. Enrollment is voluntary, confidential, and free of charge.

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Who can join

  • Live in the United States.
  • Meet the listed adult age requirement: 18 or older in 47 states and Washington, D.C.; 19 or older in Alabama and Nebraska; 21 or older in Puerto Rico and Mississippi.
  • Speak English or Spanish fluently.
  • Have sinus, balance, hearing, or headache symptoms, whether or not you have been diagnosed with migraine.

Who can't join

  • Be younger than 18 or below the listed adult age requirement where you live.

Simplified for readability. The official criteria below are what the study team uses.

Official eligibility criteria

Inclusion Criteria: * Resident of the United States of America * Age of Majority (18+ in 47 states and Washington, D.C., 19+ in Alabama and Nebraska, 21+ in Puerto Rico and Mississippi) * Fluent in English OR Spanish. * Experience sinus, vestibular auditory, and/or headache symptoms, with and without diagnosis of migraine. Exclusion Criteria: * Under 18 years of age, under age of Majority. Minors are not the population of interest for the study at this time.

Study sites (1)

RI