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Tytuł pozycji:

Long term at-home treatment with transcranial direct current stimulation (tDCS) improves symptoms of cerebellar ataxia: a case report

Tytuł:
Long term at-home treatment with transcranial direct current stimulation (tDCS) improves symptoms of cerebellar ataxia: a case report
Autorzy:
Giuseppina Pilloni
Michael Shaw
Charles Feinberg
Ashley Clayton
Maria Palmeri
Abhishek Datta
Leigh E. Charvet
Temat:
Cerebellar ataxia
Transcranial direct current stimulation (tDCS)
Cerebellar tDCS
Remotely supervised tDCS
Telerehabilitation
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Źródło:
Journal of NeuroEngineering and Rehabilitation, Vol 16, Iss 1, Pp 1-8 (2019)
Wydawca:
BMC, 2019.
Rok publikacji:
2019
Kolekcja:
LCC:Neurosciences. Biological psychiatry. Neuropsychiatry
Typ dokumentu:
article
Opis pliku:
electronic resource
Język:
English
ISSN:
1743-0003
Relacje:
http://link.springer.com/article/10.1186/s12984-019-0514-z; https://doaj.org/toc/1743-0003
DOI:
10.1186/s12984-019-0514-z
Dostęp URL:
https://doaj.org/article/8358dc3eba8b4d0dbabc5f7ad2bd257a  Link otwiera się w nowym oknie
Numer akcesji:
edsdoj.8358dc3eba8b4d0dbabc5f7ad2bd257a
Czasopismo naukowe
Abstract Background Progressive cerebellar ataxia is a neurodegenerative disorder without effective treatment options that seriously hinders quality of life. Previously, transcranial direct current stimulation (tDCS) has been demonstrated to benefit cerebellar functions (including improved motor control, learning and emotional processing) in healthy individuals and patients with neurological disorders. While tDCS is an emerging therapy, multiple daily sessions are needed for optimal clinical benefit. This case study tests the symptomatic benefit of remotely supervised tDCS (RS-tDCS) for a patient with cerebellar ataxia. Methods We report a case of a 71-year-old female patient with progressive cerebellar ataxia, who presented with unsteady gait and balance impairment, treated with tDCS. tDCS was administered using our RS-tDCS protocol and was completed daily in the patient’s home (Monday – Friday) with the help of a trained study technician. tDCS was paired with 20 min of simultaneous cognitive training, followed by 20 min of physical exercises directed by a physical therapist. Stimulation consisted of 20 min of 2.5 mA direct current targeting the cerebellum via an anodal electrode and a cathodal electrode placed over the right shoulder. The patient completed baseline and treatment end visits with neurological, cognitive, and motor (Lafayette Grooved Pegboard Test, 25 ft walk test and Timed Up and Go Test) assessments. Results The patient successfully completed sixty tDCS sessions, 59 of which were administered remotely at the patient’s home with the use of real time supervision as enabled by video conferencing. Mild improvement was observed in the patient’s gait with a 7% improvement in walking speed, which she completed without a walking-aid at treatment end, which was in stark contrast to her baseline assessment. Improvements were also achieved in manual dexterity, with an increase in pegboard scores bilaterally compared to baseline. Conclusions Results from this case report suggest that consecutively administered tDCS treatments paired with cognitive and physical exercise hold promise for improving balance, gait, and manual dexterity in patients with progressive ataxia. Remotely supervised tDCS provides home access to enable the administration over an extended period. Further controlled study in a large group of those with cerebellar ataxia is needed to replicate these findings. Trial registration ClinicalTrials.gov Identifier: NCT03049969. Registered 10 February 2017- Retrospectively registered.
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