ME/CFS Brain Fog: Cognitive Rehabilitation Trial

Recruiting N/A Interventional Study
ME/CFS ME/CFS Following EBV-associated Infectious Mononucleosis ME/CFS Following COVID-19 Chronic Fatigue Chronic Fatigue Syndrome (CFS) Brain Fog Cognitive Impairment Cognitive Dysfunction
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
30 (estimated)
Sponsor
University of Alabama at Birmingham · Other
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About This Trial
The purpose of this study is to compare two approaches to cognitive rehabilitation in adults with post-viral cognitive syndrome, which resulted in brain fog. All participants will be screened for eligibility prior to participation. Most of the procedures will take place over a phone call or secure telehealth platform (i.e., Zoom). However, participants will be asked to visit UAB on three occasions…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * diagnosis of ME/CFS that preceded cognitive complaints * mild or greater cognitive impairment * moderate or greater brain fog * some impairment in the performance of daily activities * ≥ 18 years, no upper limit if medically stable * reside in the community (as opposed to a ho…
Contacts

Madeline Rathz, BS

205-934-9768

mgrathz@uab.edu

CONTACT

Helen Bliss, BS

205-934-0433

hmbliss@uab.edu

CONTACT