经颅直流电刺激
刺激
自闭症谱系障碍
心理学
随机对照试验
前额叶皮质
自闭症
听力学
医学
发展心理学
认知
物理医学与康复
精神科
内科学
神经科学
作者
Y. Wang,Fei Wang,Yue Kong,Tianshu Gao,Qingyao Zhu,Lu Han,Bei Sun,Luyang Guan,Ziyi Zhang,Yuxin Qian,Lingxi Xu,Yun Li,Hui Fang,Jiao Gongkai,Xiaoyan Ke
摘要
Abstract The purpose of this study was to determine the effect of the Cz of high‐definition 5‐channel tDCS (HD‐tDCS) on social function in 4–12 years‐old children with autism spectrum disorder (ASD). This study was a randomized, double‐blind, pseudo‐controlled trial in which 45 ASD children were recruited and divided into three groups with sex, age, and rehabilitation treatment as control variables. Each group of 15 children with ASD was randomly administered active HD‐tDCS with the Cz as the central anode, active HD‐tDCS with the left dorsolateral prefrontal cortex (F3) as the central anode, and sham HD‐tDCS with the Cz as the central anode with 14 daily sessions in 3 weeks. The Social Responsiveness Scale Chinese Version (SRS‐Chinese Version) was compared 1 week after stimulation with values recorded 1 week prior to stimulation. At the end of treatment, both the anodal Cz and anodal left DLFPC tDCS decreased the measures of SRS‐Chinese Version. The total score of SRS‐Chinese Version decreased by 13.08%, social cognition decreased by 18.33%, and social communication decreased by 10.79%, which were significantly improved over the Cz central anode active stimulation group, especially in children with young age, and middle and low function. There was no significant change in the total score and subscale score of SRS‐Chinese Version over the Cz central anode sham stimulation group. In the F3 central anode active stimulation group, the total score of SRS‐Chinese Version decreased by 13%, autistic behavior decreased by 19.39%, and social communication decreased by 14.39%, which were all significantly improved. However, there was no significant difference in effect between the Cz and left DLPFC stimulation conditions. HD‐tDCS of the Cz central anode may be an effective treatment for social dysfunction in children with ASD.
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