The study seeks to delve into the firsthand experiences of patients diagnosed with chronic fatigue syndrome who partake in a separate clinical trial featuring a specific medical intervention. The primary emphasis will be on meticulously tracking the rates of trial completion and withdrawal among these individuals.
The data collected from this study will help improve future outcomes for all chronic fatigue syndrome patients as well as those in under-represented demographic groups.
Signed Written Informed Consent
Aged ≥ 18 years old
No prior treatment for chronic fatigue syndrome
Participant is actively receiving study therapy in another
Inability to provide written informed consent
Women of childbearing potential without a negative pregnancy test; or women who are lactating.