Cluster Headache Treatment Survey

Active, not recruiting

• Conditions: Cluster Headache

• Registration Number: NCT06011811
• Lead Sponsor: The University of Texas Health Science Center, Houston

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-06-29
• Study First Submitted: 2023-08-19
• Study First Submitted QC: 2023-08-23
• Study First Posted: 2023-08-25
• Status Verified: 2024-04
• Last Update Submitted: 2024-04-12
• Last Update Posted: 2024-04-15
• Primary Completion: 2025-06-28
• Study Completion: 2025-06-28

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 5000

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Effectiveness of cluster headache treatment as assessed by a survey	at the time of survey completion, expected to be 6-12 months

Secondary Outcome Measures

Name	Time	Method
Opinions on new cluster headache treatment as assessed by a survey	at the time of survey completion, expected to be 6-12 months

Trial Locations

Locations (1)

The University of Texas Health Science Center at Houston; 🇺🇸 Houston, Texas, United States