Effects of bihemispheric transcranial direct current stimulation on motor recovery in subacute stroke patients: a double-blind, randomized sham-controlled trial
Bihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal excitability and interhemispheric interaction. However, how tDCS affects subacute stroke recovery remains unclear. We investigated the effects of bihemisp...
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Published in | Journal of neuroengineering and rehabilitation Vol. 20; no. 1; pp. 27 - 13 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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England
BioMed Central Ltd
27.02.2023
BioMed Central BMC |
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Abstract | Bihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal excitability and interhemispheric interaction. However, how tDCS affects subacute stroke recovery remains unclear. We investigated the effects of bihemispheric tDCS on motor recovery in subacute stroke patients.
We enrolled subacute inpatients who had first-ever ischemic stroke at subcortical regions and moderate-to-severe baseline Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score 2-56. Participants between 14 and 28 days after stroke were double-blind, randomly assigned (1:1) to receive real (n = 13) or sham (n = 14) bihemispheric tDCS (with ipsilesional M1 anode and contralesional M1 cathode, 20 min, 2 mA) during task practice twice daily for 20 sessions in two weeks. Residual integrity of the ipsilesional corticospinal tract was stratified between groups. The primary efficacy outcome was the change in FMA-UE score from baseline (responder as an increase ≥ 10). The secondary measures included changes in the Action Research Arm Test (ARAT), FMA-Lower Extremity (FMA-LE) and explorative resting-state MRI functional connectivity (FC) of target regions after intervention and three months post-stroke.
Twenty-seven participants completed the study without significant adverse effects. Nineteen patients (70%) had no recordable baseline motor-evoked potentials (MEP-negative) from the paretic forearm. Compared with the sham group, the real tDCS group showed enhanced improvement of FMA-UE after intervention (p < 0.01, effect size η
= 0.211; responder rate: 77% vs. 36%, p = 0.031), which sustained three months post-stroke (p < 0.01), but not ARAT. Interestingly, in the MEP-negative subgroup analysis, the FMA-UE improvement remained but delayed. Additionally, the FMA-LE improvement after real tDCS was not significantly greater until three months post-stroke (p < 0.01). We found that the individual FMA-UE improvements after real tDCS were associated with bilateral intrahemispheric, rather than interhemispheric, FC strengths in the targeted cortices, while the improvements after sham tDCS were associated with predominantly ipsilesional FC changes after adjustment for age and sex (p < 0.01).
Bihemispheric tDCS during task-oriented training may facilitate motor recovery in subacute stroke patients, even with compromised corticospinal tract integrity. Further studies are warranted for tDCS efficacy and network-specific neuromodulation.
This study is registered with ClinicalTrials.gov: (ID: NCT02731508). |
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AbstractList | Bihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal excitability and interhemispheric interaction. However, how tDCS affects subacute stroke recovery remains unclear. We investigated the effects of bihemispheric tDCS on motor recovery in subacute stroke patients. We enrolled subacute inpatients who had first-ever ischemic stroke at subcortical regions and moderate-to-severe baseline Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score 2-56. Participants between 14 and 28 days after stroke were double-blind, randomly assigned (1:1) to receive real (n = 13) or sham (n = 14) bihemispheric tDCS (with ipsilesional M1 anode and contralesional M1 cathode, 20 min, 2 mA) during task practice twice daily for 20 sessions in two weeks. Residual integrity of the ipsilesional corticospinal tract was stratified between groups. The primary efficacy outcome was the change in FMA-UE score from baseline (responder as an increase [greater than or equal to] 10). The secondary measures included changes in the Action Research Arm Test (ARAT), FMA-Lower Extremity (FMA-LE) and explorative resting-state MRI functional connectivity (FC) of target regions after intervention and three months post-stroke. Twenty-seven participants completed the study without significant adverse effects. Nineteen patients (70%) had no recordable baseline motor-evoked potentials (MEP-negative) from the paretic forearm. Compared with the sham group, the real tDCS group showed enhanced improvement of FMA-UE after intervention (p < 0.01, effect size η.sup.2 = 0.211; responder rate: 77% vs. 36%, p = 0.031), which sustained three months post-stroke (p < 0.01), but not ARAT. Interestingly, in the MEP-negative subgroup analysis, the FMA-UE improvement remained but delayed. Additionally, the FMA-LE improvement after real tDCS was not significantly greater until three months post-stroke (p < 0.01). We found that the individual FMA-UE improvements after real tDCS were associated with bilateral intrahemispheric, rather than interhemispheric, FC strengths in the targeted cortices, while the improvements after sham tDCS were associated with predominantly ipsilesional FC changes after adjustment for age and sex (p < 0.01). Bihemispheric tDCS during task-oriented training may facilitate motor recovery in subacute stroke patients, even with compromised corticospinal tract integrity. Further studies are warranted for tDCS efficacy and network-specific neuromodulation. Bihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal excitability and interhemispheric interaction. However, how tDCS affects subacute stroke recovery remains unclear. We investigated the effects of bihemispheric tDCS on motor recovery in subacute stroke patients. We enrolled subacute inpatients who had first-ever ischemic stroke at subcortical regions and moderate-to-severe baseline Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score 2-56. Participants between 14 and 28 days after stroke were double-blind, randomly assigned (1:1) to receive real (n = 13) or sham (n = 14) bihemispheric tDCS (with ipsilesional M1 anode and contralesional M1 cathode, 20 min, 2 mA) during task practice twice daily for 20 sessions in two weeks. Residual integrity of the ipsilesional corticospinal tract was stratified between groups. The primary efficacy outcome was the change in FMA-UE score from baseline (responder as an increase ≥ 10). The secondary measures included changes in the Action Research Arm Test (ARAT), FMA-Lower Extremity (FMA-LE) and explorative resting-state MRI functional connectivity (FC) of target regions after intervention and three months post-stroke. Twenty-seven participants completed the study without significant adverse effects. Nineteen patients (70%) had no recordable baseline motor-evoked potentials (MEP-negative) from the paretic forearm. Compared with the sham group, the real tDCS group showed enhanced improvement of FMA-UE after intervention (p < 0.01, effect size η = 0.211; responder rate: 77% vs. 36%, p = 0.031), which sustained three months post-stroke (p < 0.01), but not ARAT. Interestingly, in the MEP-negative subgroup analysis, the FMA-UE improvement remained but delayed. Additionally, the FMA-LE improvement after real tDCS was not significantly greater until three months post-stroke (p < 0.01). We found that the individual FMA-UE improvements after real tDCS were associated with bilateral intrahemispheric, rather than interhemispheric, FC strengths in the targeted cortices, while the improvements after sham tDCS were associated with predominantly ipsilesional FC changes after adjustment for age and sex (p < 0.01). Bihemispheric tDCS during task-oriented training may facilitate motor recovery in subacute stroke patients, even with compromised corticospinal tract integrity. Further studies are warranted for tDCS efficacy and network-specific neuromodulation. This study is registered with ClinicalTrials.gov: (ID: NCT02731508). Background Bihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal excitability and interhemispheric interaction. However, how tDCS affects subacute stroke recovery remains unclear. We investigated the effects of bihemispheric tDCS on motor recovery in subacute stroke patients. Methods We enrolled subacute inpatients who had first-ever ischemic stroke at subcortical regions and moderate-to-severe baseline Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score 2-56. Participants between 14 and 28 days after stroke were double-blind, randomly assigned (1:1) to receive real (n = 13) or sham (n = 14) bihemispheric tDCS (with ipsilesional M1 anode and contralesional M1 cathode, 20 min, 2 mA) during task practice twice daily for 20 sessions in two weeks. Residual integrity of the ipsilesional corticospinal tract was stratified between groups. The primary efficacy outcome was the change in FMA-UE score from baseline (responder as an increase [greater than or equal to] 10). The secondary measures included changes in the Action Research Arm Test (ARAT), FMA-Lower Extremity (FMA-LE) and explorative resting-state MRI functional connectivity (FC) of target regions after intervention and three months post-stroke. Results Twenty-seven participants completed the study without significant adverse effects. Nineteen patients (70%) had no recordable baseline motor-evoked potentials (MEP-negative) from the paretic forearm. Compared with the sham group, the real tDCS group showed enhanced improvement of FMA-UE after intervention (p < 0.01, effect size η.sup.2 = 0.211; responder rate: 77% vs. 36%, p = 0.031), which sustained three months post-stroke (p < 0.01), but not ARAT. Interestingly, in the MEP-negative subgroup analysis, the FMA-UE improvement remained but delayed. Additionally, the FMA-LE improvement after real tDCS was not significantly greater until three months post-stroke (p < 0.01). We found that the individual FMA-UE improvements after real tDCS were associated with bilateral intrahemispheric, rather than interhemispheric, FC strengths in the targeted cortices, while the improvements after sham tDCS were associated with predominantly ipsilesional FC changes after adjustment for age and sex (p < 0.01). Conclusions Bihemispheric tDCS during task-oriented training may facilitate motor recovery in subacute stroke patients, even with compromised corticospinal tract integrity. Further studies are warranted for tDCS efficacy and network-specific neuromodulation. Trial registration: This study is registered with ClinicalTrials.gov: (ID: NCT02731508). Keywords: Dual, Functional connectivity, Motor, Neuroplasticity, Stroke, tDCS, Upper extremity Abstract Background Bihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal excitability and interhemispheric interaction. However, how tDCS affects subacute stroke recovery remains unclear. We investigated the effects of bihemispheric tDCS on motor recovery in subacute stroke patients. Methods We enrolled subacute inpatients who had first-ever ischemic stroke at subcortical regions and moderate-to-severe baseline Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score 2–56. Participants between 14 and 28 days after stroke were double-blind, randomly assigned (1:1) to receive real (n = 13) or sham (n = 14) bihemispheric tDCS (with ipsilesional M1 anode and contralesional M1 cathode, 20 min, 2 mA) during task practice twice daily for 20 sessions in two weeks. Residual integrity of the ipsilesional corticospinal tract was stratified between groups. The primary efficacy outcome was the change in FMA-UE score from baseline (responder as an increase ≥ 10). The secondary measures included changes in the Action Research Arm Test (ARAT), FMA-Lower Extremity (FMA-LE) and explorative resting-state MRI functional connectivity (FC) of target regions after intervention and three months post-stroke. Results Twenty-seven participants completed the study without significant adverse effects. Nineteen patients (70%) had no recordable baseline motor-evoked potentials (MEP-negative) from the paretic forearm. Compared with the sham group, the real tDCS group showed enhanced improvement of FMA-UE after intervention (p < 0.01, effect size η 2 = 0.211; responder rate: 77% vs. 36%, p = 0.031), which sustained three months post-stroke (p < 0.01), but not ARAT. Interestingly, in the MEP-negative subgroup analysis, the FMA-UE improvement remained but delayed. Additionally, the FMA-LE improvement after real tDCS was not significantly greater until three months post-stroke (p < 0.01). We found that the individual FMA-UE improvements after real tDCS were associated with bilateral intrahemispheric, rather than interhemispheric, FC strengths in the targeted cortices, while the improvements after sham tDCS were associated with predominantly ipsilesional FC changes after adjustment for age and sex (p < 0.01). Conclusions Bihemispheric tDCS during task-oriented training may facilitate motor recovery in subacute stroke patients, even with compromised corticospinal tract integrity. Further studies are warranted for tDCS efficacy and network-specific neuromodulation. Trial registration: This study is registered with ClinicalTrials.gov: (ID: NCT02731508). BackgroundBihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal excitability and interhemispheric interaction. However, how tDCS affects subacute stroke recovery remains unclear. We investigated the effects of bihemispheric tDCS on motor recovery in subacute stroke patients.MethodsWe enrolled subacute inpatients who had first-ever ischemic stroke at subcortical regions and moderate-to-severe baseline Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score 2–56. Participants between 14 and 28 days after stroke were double-blind, randomly assigned (1:1) to receive real (n = 13) or sham (n = 14) bihemispheric tDCS (with ipsilesional M1 anode and contralesional M1 cathode, 20 min, 2 mA) during task practice twice daily for 20 sessions in two weeks. Residual integrity of the ipsilesional corticospinal tract was stratified between groups. The primary efficacy outcome was the change in FMA-UE score from baseline (responder as an increase ≥ 10). The secondary measures included changes in the Action Research Arm Test (ARAT), FMA-Lower Extremity (FMA-LE) and explorative resting-state MRI functional connectivity (FC) of target regions after intervention and three months post-stroke.ResultsTwenty-seven participants completed the study without significant adverse effects. Nineteen patients (70%) had no recordable baseline motor-evoked potentials (MEP-negative) from the paretic forearm. Compared with the sham group, the real tDCS group showed enhanced improvement of FMA-UE after intervention (p < 0.01, effect size η2 = 0.211; responder rate: 77% vs. 36%, p = 0.031), which sustained three months post-stroke (p < 0.01), but not ARAT. Interestingly, in the MEP-negative subgroup analysis, the FMA-UE improvement remained but delayed. Additionally, the FMA-LE improvement after real tDCS was not significantly greater until three months post-stroke (p < 0.01). We found that the individual FMA-UE improvements after real tDCS were associated with bilateral intrahemispheric, rather than interhemispheric, FC strengths in the targeted cortices, while the improvements after sham tDCS were associated with predominantly ipsilesional FC changes after adjustment for age and sex (p < 0.01).ConclusionsBihemispheric tDCS during task-oriented training may facilitate motor recovery in subacute stroke patients, even with compromised corticospinal tract integrity. Further studies are warranted for tDCS efficacy and network-specific neuromodulation.Trial registration: This study is registered with ClinicalTrials.gov: (ID: NCT02731508). Bihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal excitability and interhemispheric interaction. However, how tDCS affects subacute stroke recovery remains unclear. We investigated the effects of bihemispheric tDCS on motor recovery in subacute stroke patients.BACKGROUNDBihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal excitability and interhemispheric interaction. However, how tDCS affects subacute stroke recovery remains unclear. We investigated the effects of bihemispheric tDCS on motor recovery in subacute stroke patients.We enrolled subacute inpatients who had first-ever ischemic stroke at subcortical regions and moderate-to-severe baseline Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score 2-56. Participants between 14 and 28 days after stroke were double-blind, randomly assigned (1:1) to receive real (n = 13) or sham (n = 14) bihemispheric tDCS (with ipsilesional M1 anode and contralesional M1 cathode, 20 min, 2 mA) during task practice twice daily for 20 sessions in two weeks. Residual integrity of the ipsilesional corticospinal tract was stratified between groups. The primary efficacy outcome was the change in FMA-UE score from baseline (responder as an increase ≥ 10). The secondary measures included changes in the Action Research Arm Test (ARAT), FMA-Lower Extremity (FMA-LE) and explorative resting-state MRI functional connectivity (FC) of target regions after intervention and three months post-stroke.METHODSWe enrolled subacute inpatients who had first-ever ischemic stroke at subcortical regions and moderate-to-severe baseline Fugl-Meyer Assessment of Upper Extremity (FMA-UE) score 2-56. Participants between 14 and 28 days after stroke were double-blind, randomly assigned (1:1) to receive real (n = 13) or sham (n = 14) bihemispheric tDCS (with ipsilesional M1 anode and contralesional M1 cathode, 20 min, 2 mA) during task practice twice daily for 20 sessions in two weeks. Residual integrity of the ipsilesional corticospinal tract was stratified between groups. The primary efficacy outcome was the change in FMA-UE score from baseline (responder as an increase ≥ 10). The secondary measures included changes in the Action Research Arm Test (ARAT), FMA-Lower Extremity (FMA-LE) and explorative resting-state MRI functional connectivity (FC) of target regions after intervention and three months post-stroke.Twenty-seven participants completed the study without significant adverse effects. Nineteen patients (70%) had no recordable baseline motor-evoked potentials (MEP-negative) from the paretic forearm. Compared with the sham group, the real tDCS group showed enhanced improvement of FMA-UE after intervention (p < 0.01, effect size η2 = 0.211; responder rate: 77% vs. 36%, p = 0.031), which sustained three months post-stroke (p < 0.01), but not ARAT. Interestingly, in the MEP-negative subgroup analysis, the FMA-UE improvement remained but delayed. Additionally, the FMA-LE improvement after real tDCS was not significantly greater until three months post-stroke (p < 0.01). We found that the individual FMA-UE improvements after real tDCS were associated with bilateral intrahemispheric, rather than interhemispheric, FC strengths in the targeted cortices, while the improvements after sham tDCS were associated with predominantly ipsilesional FC changes after adjustment for age and sex (p < 0.01).RESULTSTwenty-seven participants completed the study without significant adverse effects. Nineteen patients (70%) had no recordable baseline motor-evoked potentials (MEP-negative) from the paretic forearm. Compared with the sham group, the real tDCS group showed enhanced improvement of FMA-UE after intervention (p < 0.01, effect size η2 = 0.211; responder rate: 77% vs. 36%, p = 0.031), which sustained three months post-stroke (p < 0.01), but not ARAT. Interestingly, in the MEP-negative subgroup analysis, the FMA-UE improvement remained but delayed. Additionally, the FMA-LE improvement after real tDCS was not significantly greater until three months post-stroke (p < 0.01). We found that the individual FMA-UE improvements after real tDCS were associated with bilateral intrahemispheric, rather than interhemispheric, FC strengths in the targeted cortices, while the improvements after sham tDCS were associated with predominantly ipsilesional FC changes after adjustment for age and sex (p < 0.01).Bihemispheric tDCS during task-oriented training may facilitate motor recovery in subacute stroke patients, even with compromised corticospinal tract integrity. Further studies are warranted for tDCS efficacy and network-specific neuromodulation.CONCLUSIONSBihemispheric tDCS during task-oriented training may facilitate motor recovery in subacute stroke patients, even with compromised corticospinal tract integrity. Further studies are warranted for tDCS efficacy and network-specific neuromodulation.This study is registered with ClinicalTrials.gov: (ID: NCT02731508).TRIAL REGISTRATIONThis study is registered with ClinicalTrials.gov: (ID: NCT02731508). |
ArticleNumber | 27 |
Audience | Academic |
Author | Shyu, Kuo-Kai Lee, I-Hui Niddam, David M. Hsu, Shih-Pin Tang, Chih-Wei Lin, Bing-Fong Tsai, Yun-An Kuo, I-Ju Lu, Chia-Feng Lee, Po-Lei Guo, Chao-Yu |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36849990$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1177/1545968311411054 10.1016/j.neuroimage.2021.118144 10.1212/WNL.0b013e318202013a 10.3389/fneur.2022.809843 10.1007/s40120-021-00300-0 10.1523/JNEUROSCI.3414-16.2017 10.1017/S1461145710001690 10.1111/j.1469-7793.2000.t01-1-00633.x 10.1113/jphysiol.2012.249730 10.1111/ner.12574 10.1002/ana.24472 10.1002/ana.25679 10.1126/scitranslmed.aad5651 10.1186/s12984-020-00706-1 10.2522/ptj.20080285 10.1038/srep23271 10.1016/j.brs.2019.10.019 10.1113/JP272738 10.1177/1545968311413906 10.1177/1545968321992330 10.1016/j.neuroimage.2011.01.014 10.1002/hbm.21266 10.1007/s10548-018-0644-9 10.1111/ene.14451 10.1161/STROKEAHA.119.027126 10.1016/j.brs.2022.12.008 10.1016/j.brs.2017.03.008 10.2340/1650197771331 10.1016/j.brs.2015.09.002 10.1007/s00221-019-05477-3 10.3389/fnhum.2016.00258 10.1310/tsr18s01-599 10.1161/01.STR.19.5.604 10.1073/pnas.1002431107 10.1007/s00234-016-1646-5 10.1016/j.cortex.2019.04.016 10.1016/j.neuroimage.2011.10.023 10.1177/1545968311411056 10.1212/WNL.0000000000012187 10.1002/ana.21905 10.1016/S0197-2456(02)00242-8 10.1002/oti.275 10.1097/00004356-198112000-00001 10.1177/0271678X211002968 10.1109/TNSRE.2019.2920576 10.1038/nrn2735 10.1002/ana.24510 10.1016/j.brs.2014.10.001 10.1016/j.clinph.2021.05.015 10.2340/jrm.v54.3208 10.1016/j.apmr.2006.02.036 10.1016/j.jstrokecerebrovasdis.2019.104454 10.1161/STROKEAHA.111.645614 10.1177/1545968312448234 10.1155/2016/5068127 10.1016/j.clinph.2014.01.034 |
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Copyright | 2023. The Author(s). COPYRIGHT 2023 BioMed Central Ltd. 2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. The Author(s) 2023 |
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Keywords | Functional connectivity Neuroplasticity Stroke Motor tDCS Dual Upper extremity |
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References | MH Rabadi (1153_CR53) 2006; 87 TH Murphy (1153_CR24) 2009; 10 BF Lin (1153_CR47) 2022; 13 N Bolognini (1153_CR3) 2020 ES Powell (1153_CR30) 2019; 1 WD Byblow (1153_CR27) 2015; 78 JH Lin (1153_CR52) 2009; 89 M van Assche (1153_CR12) 2021; 41 AB Shinde (1153_CR56) 2021; 237 G Batsikadze (1153_CR9) 2013; 591 J Lee (1153_CR36) 2018; 31 AR Brunoni (1153_CR42) 2011; 14 PW Chang (1153_CR62) 2022; 11 AK Rehme (1153_CR13) 2012; 59 R Lindenberg (1153_CR59) 2012; 33 M Mosayebi Samani (1153_CR8) 2019; 119 S Mazzoleni (1153_CR1) 2019; 27 MM Garrido (1153_CR23) 2023; 16 W Klomjai (1153_CR22) 2022; 54 R van der Vliet (1153_CR40) 2020; 87 S Hesse (1153_CR2) 2011; 25 S Bornheim (1153_CR4) 2020; 13 Y Zhang (1153_CR37) 2016; 58 U Takechi (1153_CR15) 2014; 125 S Van Hoornweder (1153_CR16) 2021; 132 KN Arya (1153_CR43) 2011; 18 PY Chhatbar (1153_CR32) 2016; 9 M Alt Murphy (1153_CR54) 2012; 26 N Bolognini (1153_CR18) 2011; 25 C Allman (1153_CR34) 2016; 8 HL Cheng (1153_CR46) 2012; 43 AK Rehme (1153_CR14) 2011; 55 AR Carter (1153_CR57) 2012; 26 AR Carter (1153_CR35) 2010; 67 AM Goodwill (1153_CR31) 2016; 10 J Cohen (1153_CR49) 1988 LD Beaulieu (1153_CR20) 2019; 37 C Russo (1153_CR51) 2017; 20 V Di Lazzaro (1153_CR5) 2014; 7 G Shilo (1153_CR10) 2019; 237 JC van Swieten (1153_CR45) 1988; 19 B Hordacre (1153_CR25) 2021; 35 J Cohen (1153_CR50) 2003 MN McDonnell (1153_CR11) 2017; 10 B Hordacre (1153_CR26) 2021; 97 AR Fugl-Meyer (1153_CR38) 1975; 7 C Kemlin (1153_CR28) 2019; 50 S Waters (1153_CR55) 2017; 37 MA Nitsche (1153_CR6) 2000; 527 IJ Hubbard (1153_CR41) 2009; 16 IJ Kuo (1153_CR33) 2020; 17 A Jamil (1153_CR7) 2017; 595 EM Nomura (1153_CR61) 2010; 107 NW Scott (1153_CR39) 2002; 23 S Straudi (1153_CR19) 2016; 2016 JL Chen (1153_CR58) 2016; 6 DJ Edwards (1153_CR29) 2019; 37 L Portney (1153_CR48) 2009 W Feng (1153_CR60) 2015; 78 RC Lyle (1153_CR44) 1981; 4 R Lindenberg (1153_CR17) 2010; 75 DC Alisar (1153_CR21) 2020; 29 |
References_xml | – volume: 26 start-page: 7 year: 2012 ident: 1153_CR57 publication-title: Neurorehabil Neural Repair doi: 10.1177/1545968311411054 – volume: 237 year: 2021 ident: 1153_CR56 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2021.118144 – volume: 75 start-page: 2176 year: 2010 ident: 1153_CR17 publication-title: Neurology doi: 10.1212/WNL.0b013e318202013a – volume: 13 year: 2022 ident: 1153_CR47 publication-title: Front Neurol doi: 10.3389/fneur.2022.809843 – volume: 11 start-page: 103 year: 2022 ident: 1153_CR62 publication-title: Neurol Therapy doi: 10.1007/s40120-021-00300-0 – volume-title: Foundations of clinical research: applications to practice year: 2009 ident: 1153_CR48 – volume: 37 start-page: 7500 year: 2017 ident: 1153_CR55 publication-title: J Neurosci doi: 10.1523/JNEUROSCI.3414-16.2017 – volume: 14 start-page: 1133 year: 2011 ident: 1153_CR42 publication-title: Int J Neuropsychopharmacol doi: 10.1017/S1461145710001690 – volume: 527 start-page: 633 issue: Pt 3 year: 2000 ident: 1153_CR6 publication-title: J Physiol doi: 10.1111/j.1469-7793.2000.t01-1-00633.x – volume: 591 start-page: 1987 year: 2013 ident: 1153_CR9 publication-title: J Physiol doi: 10.1113/jphysiol.2012.249730 – volume: 20 start-page: 215 year: 2017 ident: 1153_CR51 publication-title: Neuromodulation doi: 10.1111/ner.12574 – volume: 78 start-page: 848 year: 2015 ident: 1153_CR27 publication-title: Ann Neurol doi: 10.1002/ana.24472 – volume: 87 start-page: 383 year: 2020 ident: 1153_CR40 publication-title: Ann Neurol doi: 10.1002/ana.25679 – volume: 8 start-page: 330re1 year: 2016 ident: 1153_CR34 publication-title: Sci Transl Med. doi: 10.1126/scitranslmed.aad5651 – volume: 17 start-page: 72 year: 2020 ident: 1153_CR33 publication-title: J Neuroeng Rehabil doi: 10.1186/s12984-020-00706-1 – volume: 37 start-page: 167 year: 2019 ident: 1153_CR29 publication-title: Restor Neurol Neurosci – volume: 89 start-page: 840 year: 2009 ident: 1153_CR52 publication-title: Phys Ther doi: 10.2522/ptj.20080285 – volume: 6 start-page: 23271 year: 2016 ident: 1153_CR58 publication-title: Sci Rep doi: 10.1038/srep23271 – volume: 13 start-page: 329 year: 2020 ident: 1153_CR4 publication-title: Brain Stimul doi: 10.1016/j.brs.2019.10.019 – volume-title: Statistical power analysis for the behavioral sciences year: 1988 ident: 1153_CR49 – volume: 595 start-page: 1273 year: 2017 ident: 1153_CR7 publication-title: J Physiol doi: 10.1113/JP272738 – volume: 25 start-page: 838 year: 2011 ident: 1153_CR2 publication-title: Neurorehabil Neural Repair doi: 10.1177/1545968311413906 – volume: 35 start-page: 307 year: 2021 ident: 1153_CR25 publication-title: Neurorehabil Neural Repair doi: 10.1177/1545968321992330 – volume: 55 start-page: 1147 year: 2011 ident: 1153_CR14 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2011.01.014 – volume: 33 start-page: 1040 year: 2012 ident: 1153_CR59 publication-title: Hum Brain Mapp doi: 10.1002/hbm.21266 – volume: 31 start-page: 708 year: 2018 ident: 1153_CR36 publication-title: Brain Topogr doi: 10.1007/s10548-018-0644-9 – year: 2020 ident: 1153_CR3 publication-title: Eur J Neurol. doi: 10.1111/ene.14451 – volume: 50 start-page: 3647 year: 2019 ident: 1153_CR28 publication-title: Stroke doi: 10.1161/STROKEAHA.119.027126 – volume: 16 start-page: 40 year: 2023 ident: 1153_CR23 publication-title: Brain Stimul doi: 10.1016/j.brs.2022.12.008 – volume: 10 start-page: 721 year: 2017 ident: 1153_CR11 publication-title: Brain Stimul doi: 10.1016/j.brs.2017.03.008 – volume: 7 start-page: 13 year: 1975 ident: 1153_CR38 publication-title: Scand J Rehabil Med. doi: 10.2340/1650197771331 – volume: 9 start-page: 16 year: 2016 ident: 1153_CR32 publication-title: Brain Stimul doi: 10.1016/j.brs.2015.09.002 – volume: 237 start-page: 919 year: 2019 ident: 1153_CR10 publication-title: Exp Brain Res doi: 10.1007/s00221-019-05477-3 – volume: 10 start-page: 258 year: 2016 ident: 1153_CR31 publication-title: Front Hum Neurosci doi: 10.3389/fnhum.2016.00258 – volume: 18 start-page: 599 issue: Suppl 1 year: 2011 ident: 1153_CR43 publication-title: Top Stroke Rehabil doi: 10.1310/tsr18s01-599 – volume: 19 start-page: 604 year: 1988 ident: 1153_CR45 publication-title: Stroke doi: 10.1161/01.STR.19.5.604 – volume: 107 start-page: 12017 year: 2010 ident: 1153_CR61 publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.1002431107 – volume: 58 start-page: 503 year: 2016 ident: 1153_CR37 publication-title: Neuroradiology doi: 10.1007/s00234-016-1646-5 – volume: 119 start-page: 350 year: 2019 ident: 1153_CR8 publication-title: Cortex doi: 10.1016/j.cortex.2019.04.016 – volume: 59 start-page: 2771 year: 2012 ident: 1153_CR13 publication-title: Neuroimage doi: 10.1016/j.neuroimage.2011.10.023 – volume: 25 start-page: 819 year: 2011 ident: 1153_CR18 publication-title: Neurorehabil Neural Repair doi: 10.1177/1545968311411056 – volume: 97 start-page: 170 year: 2021 ident: 1153_CR26 publication-title: Neurology doi: 10.1212/WNL.0000000000012187 – volume: 67 start-page: 365 year: 2010 ident: 1153_CR35 publication-title: Ann Neurol doi: 10.1002/ana.21905 – volume: 23 start-page: 662 year: 2002 ident: 1153_CR39 publication-title: Control Clin Trials doi: 10.1016/S0197-2456(02)00242-8 – volume: 16 start-page: 175 year: 2009 ident: 1153_CR41 publication-title: Occup Ther Int doi: 10.1002/oti.275 – volume: 4 start-page: 483 year: 1981 ident: 1153_CR44 publication-title: Int J Rehabil Res doi: 10.1097/00004356-198112000-00001 – volume: 41 start-page: 2174 year: 2021 ident: 1153_CR12 publication-title: J Cereb Blood Flow Metab doi: 10.1177/0271678X211002968 – volume: 27 start-page: 1458 year: 2019 ident: 1153_CR1 publication-title: IEEE Trans Neural Syst Rehabil Eng doi: 10.1109/TNSRE.2019.2920576 – volume: 10 start-page: 861 year: 2009 ident: 1153_CR24 publication-title: Nat Rev Neurosci doi: 10.1038/nrn2735 – volume-title: Apllied multiple regession/correlation analysis for the behavioral sciences year: 2003 ident: 1153_CR50 – volume: 1 year: 2019 ident: 1153_CR30 publication-title: Arch Rehabil Res Clin Transl – volume: 78 start-page: 860 year: 2015 ident: 1153_CR60 publication-title: Ann Neurol doi: 10.1002/ana.24510 – volume: 7 start-page: 841 year: 2014 ident: 1153_CR5 publication-title: Brain Stimul doi: 10.1016/j.brs.2014.10.001 – volume: 132 start-page: 1897 year: 2021 ident: 1153_CR16 publication-title: Clin Neurophysiol doi: 10.1016/j.clinph.2021.05.015 – volume: 54 start-page: jrm00331 year: 2022 ident: 1153_CR22 publication-title: J Rehabil Med. doi: 10.2340/jrm.v54.3208 – volume: 87 start-page: 962 year: 2006 ident: 1153_CR53 publication-title: Arch Phys Med Rehabil doi: 10.1016/j.apmr.2006.02.036 – volume: 29 year: 2020 ident: 1153_CR21 publication-title: J Stroke Cerebrovasc Dis doi: 10.1016/j.jstrokecerebrovasdis.2019.104454 – volume: 43 start-page: 2567 year: 2012 ident: 1153_CR46 publication-title: Stroke doi: 10.1161/STROKEAHA.111.645614 – volume: 26 start-page: 1106 year: 2012 ident: 1153_CR54 publication-title: Neurorehabil Neural Repair doi: 10.1177/1545968312448234 – volume: 2016 start-page: 5068127 year: 2016 ident: 1153_CR19 publication-title: Biomed Res Int doi: 10.1155/2016/5068127 – volume: 37 start-page: 333 year: 2019 ident: 1153_CR20 publication-title: Restor Neurol Neurosci – volume: 125 start-page: 2055 year: 2014 ident: 1153_CR15 publication-title: Clin Neurophysiol doi: 10.1016/j.clinph.2014.01.034 |
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Snippet | Bihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal excitability... Background Bihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal... BackgroundBihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral corticospinal... Abstract Background Bihemispheric transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) can simultaneously modulate bilateral... |
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SubjectTerms | Biomarkers Brain stimulation Care and treatment Cerebral Cortex Cerebral hemispheres Cortex (motor) Direct current Double-Blind Method Double-blind studies Dual Effectiveness Electrical stimulation of the brain Electrical stimuli ESB Excitability Functional connectivity Functional magnetic resonance imaging Health aspects Humans Inpatients Integrity Ischemia Motor Motor cortex Motor evoked potentials Neural networks Neurologic manifestations of general diseases Neuromodulation Neuroplasticity Occupational therapy Pyramidal tracts Stimulation Stroke Stroke patients Subgroups tDCS Testing Transcranial Direct Current Stimulation Transcranial magnetic stimulation |
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Title | Effects of bihemispheric transcranial direct current stimulation on motor recovery in subacute stroke patients: a double-blind, randomized sham-controlled trial |
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