Cluster Headache Treatment Survey

N/AActive Not RecruitingNCT06011811

The University of Texas Health Science Center, Houston5,000 enrolled

Overview

The objective of this study is to survey patients with cluster headache about treatment effectiveness and their views on treatments. Participants will complete one brief questionnaire online.

Study Type

OBSERVATIONAL

Enrollment

5,000

Conditions

Cluster Headache

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients with episodic or chronic cluster headache that has been diagnosed by a health care professional (no documentation is needed, participant must simply state that he or she has been diagnosed) Exclusion Criteria: * Unable to speak English (the survey is only in English) * Unable to use a computer to take the online survey * Unable to provide consent

Locations (1)

The University of Texas Health Science Center at Houston

Houston, Texas, United States

Outcomes

Primary Outcomes

Effectiveness of cluster headache treatment as assessed by a survey

Time frame: at the time of survey completion, expected to be 6-12 months

Secondary Outcomes

Opinions on new cluster headache treatment as assessed by a survey

Time frame: at the time of survey completion, expected to be 6-12 months

Data from ClinicalTrials.gov

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