2023
DOI: 10.1161/strokeaha.122.041557
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Transcranial Direct-Current Stimulation in Subacute Aphasia: A Randomized Controlled Trial

Abstract: Background: Transcranial direct-current stimulation (tDCS) is a promising adjunct to therapy for chronic aphasia. Methods: This single-center, randomized, double-blind, sham-controlled efficacy trial tested the hypothesis that anodal tDCS augments language therapy in subacute aphasia. Secondarily, we compared the effect of tDCS on discourse measures and quality of life and compared the effects on naming to previous findings in chronic stroke. Right-hand… Show more

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Cited by 11 publications
(8 citation statements)
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“…We also administered the Stroke Impact Scale 25 (SIS), a disease-specific quality of life questionnaire. 9 All participants with no contraindication were asked to complete structural and functional magnetic resonance imaging (fMRI) to support localization of the lesion and identification of a stimulation site of healthy tissue. If they consented to research MRI, they were randomized to (1) have the site of stimulation based on greatest area of activation on fMRI during a naming task (as in Fridriksson et al 26 ) or (2) have the site of stimulation based on the area of lesion (from clinical imaging or research MRI).…”
Section: Discussionmentioning
confidence: 99%
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“…We also administered the Stroke Impact Scale 25 (SIS), a disease-specific quality of life questionnaire. 9 All participants with no contraindication were asked to complete structural and functional magnetic resonance imaging (fMRI) to support localization of the lesion and identification of a stimulation site of healthy tissue. If they consented to research MRI, they were randomized to (1) have the site of stimulation based on greatest area of activation on fMRI during a naming task (as in Fridriksson et al 26 ) or (2) have the site of stimulation based on the area of lesion (from clinical imaging or research MRI).…”
Section: Discussionmentioning
confidence: 99%
“…Two planned exploratory subgroup analyses were conducted on the sample of study completers to follow up with the primary outcome findings. 9 The first analysis examined the influence of age (<55 vs ≥55 years), sex, education (<11 years completed vs ≥12 years), and time since stroke onset to initiation of CoDeLT (<1 month vs ≥1 month), and BDNF status on response to CoDeLT by treatment group (collapsing across stimulation sites that targeted healthy tissue). The software package SAS was used.…”
Section: Discussionmentioning
confidence: 99%
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