Cluster Headache
Conditions
Keywords
Cluster Headache
Brief summary
Historically, participation in clinical studies is highly skewed towards particular demographic groups of people. This research will invite several participants to gather a wide range of information on clinical trial experiences for cluster headache patients. The aim of the study is to identify the factors that limit the ability of a person to enroll in, as well as complete a clinical trial for treatment of cluster headache. The data collected from this study will help improve future outcomes for all cluster headache patients as well as those in under-represented demographic groups.
Interventions
None listed
Sponsors
Power Life Sciences Inc.
Study design
Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patient has been diagnosed with cluster headache * Patient has access to a home internet connection in order to provide regular updates through the course of the study * Participant must be 18 years of age or older
Exclusion criteria
* Patient has an ECOG score of 4 or higher * Patient is not able to provide consistent digital updates as per study requirements * Patient does not complete or agree to terms outlined in the Informed Consent Form
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of patients who decide to enroll in a cluster headache clinical study. | 3 months |
| Number of cluster headache patients who remain in clinical research until completion. | 12 months |
Countries
United States
Contacts
Primary ContactMichael B Gill
Outcome results
None listed