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This one-arm open-label interventional study will investigate the effects of transcranial direct current stimulation in an remote home-based setting with the aims to evaluate the feasibility (usability of the device, compliance of patients, usability of the teletherapy), the effectiveness (clinical ratings) and the compatability of this intervention in 20 patients with ME/CFS.
(Description adapted from clinical trial website: see link above)
ME/CFS according to Canadian Consensus Criteria (CCC).
Patients enrolled: 20
Age group: 18 - 70 years (Older Adults, Adults)