A multicenter, randomized, double-blind, placebo-controlled trial to test efficacy and safety of transcranial direct current stimulation to the motor cortex after stroke (NETS): study protocol
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Published:2022-04-18
Issue:1
Volume:4
Page:
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ISSN:2524-3489
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Container-title:Neurological Research and Practice
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language:en
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Short-container-title:Neurol. Res. Pract.
Author:
, Gerloff ChristianORCID, Heise Kirstin-Friederike, Schulz Robert, Hummel Friedhelm C., Wolf Silke, Zapf Antonia, Cordes Diana, Gerloff Christian, Heise Kirstin-Friederike, Hummel Friedhelm, Schulz Robert, Wolf Silke, Haevernick Kerstin, Krüger Heike, Krause Linda, Suling Anna, Wegscheider Karl, Zapf Antonia, Dressnandt Jürgen, Schäpers Barbara, Schrödl Christoph, Hauptmann Björn, Kirchner Anja, Brault Anna, Gutschalk Alexander, Richter Constanze, Nowak Dennis A., Veldema Jitka, Koch Giacomo, Maiella Michele, Dohle Christian, Jettkowski Katrin, Pilz Mario, Hamzei Farsin, Olischer Lydia, Renner Caroline, Groß Marcus, Jöbges Michael, Voller Bernhard, ,
Abstract
Abstract
Introduction
The WHO estimates that each year 5 million people are left permanently disabled after stroke. Adjuvant treatments to promote the effects of rehabilitation are urgently needed. Cortical excitability and neuroplasticity can be enhanced by non-invasive brain stimulation but evidence from sufficiently powered, randomized controlled multi-center clinical trials is absent.
Methods
Neuroregeneration enhanced by transcranial direct current stimulation (tDCS) in stroke (NETS) tested efficacy and safety of anodal tDCS to the primary motor cortex of the lesioned hemisphere in the subacute phase (day 5–45) after cerebral ischemia. Stimulation was combined with standardized rehabilitative training and repeatedly applied in 10 sessions over a period of 2 weeks in a planned sample of 120 patients. Primary outcome parameter was upper-extremity function at the end of the 2-weeks intervention period of active treatment or placebo (1:1 randomization), measured by the upper-extremity Fugl-Meyer assessment. Sustainability of the treatment effect was evaluated by additional follow-up visits after 30 and 90 days. Further secondary endpoints included metrics of arm and hand function, stroke impact scale, and the depression module of the patient health questionnaire.
Perspective
NETS was aimed at providing evidence for an effective and safe adjuvant treatment for patients after stroke.
Trial registration: ClinicalTrials.gov Identifier NCT00909714. Registered May 28, 2009.
Funder
Deutsche Forschungsgemeinschaft
Publisher
Springer Science and Business Media LLC
Subject
Automotive Engineering
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