Fatigue is common and disabling in patients with post-COVID syndrome. There is no treatment available at this moment, and fatigue has important consequences. The main aim of this study is to evaluate the changes in the severity of fatigue using non-invasive neuromodulation in patients with post-COVID condition. This is a randomized, parallel, double-blind, placebo-controlled clinical trial using transcranial direct current stimulation. Secondary aims include changes in cognition, depression, and quality of life.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
47
Eight sessions of transcranial current direct stimulation
Eight sessions of transcranial current direct stimulation (sham)
Hospital Clínico San Carlos.
Madrid, Spain
Change in Fatigue
Modified Fatigue Impact Scale (MFIS)
Time frame: 2 weeks
Change in cognition
Stroop Test
Time frame: 2 weeks
Change in depressive symptoms
Beck Depression Inventory II
Time frame: 2 weeks
Change in quality of life
EuroQuol-5D
Time frame: 2 weeks
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