A Close Examination of Patient Experiences in Cluster Headache Clinical Research

N/ANot Yet RecruitingNCT05978258

Power Life Sciences Inc.500 enrolled

Overview

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.

Study Type

OBSERVATIONAL

Enrollment

500

Conditions

Cluster Headache

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Locations (1)

Power Life Sciences

San Francisco, California, United States

Outcomes

Primary Outcomes

Rate of patients who decide to enroll in a cluster headache clinical study.

Time frame: 3 months

Number of cluster headache patients who remain in clinical research until completion.

Time frame: 12 months