Effect of tDCS combined with virtual reality for post-stroke cognitive impairment: a randomized controlled trial study protocol

被引:0
|
作者
Cheng, Xiao-Ping [1 ]
Wang, Zhao-Di [2 ]
Zhou, Yue-Zhu [1 ]
Zhan, Li-Qiong [1 ]
Wu, Di [1 ]
Xie, Li-Li [1 ]
Luo, Kai-Liang [1 ]
He, Jin-Peng [3 ,4 ]
Lin, Wei [5 ]
Ni, Jun [1 ]
Lv, Lan [1 ]
Chen, Xin-Yuan [1 ,6 ]
机构
[1] Fujian Med Univ, Dept Rehabil Med, Affiliated Hosp 1, Fuzhou 350005, Peoples R China
[2] Nanjing Med Univ, Suzhou Municipal Hosp, Dept Rehabil Med, Affiliated Suzhou Hosp, Suzhou 215008, Peoples R China
[3] First Peoples Hosp Yancheng, Dept Rehabil Med, Yancheng, Peoples R China
[4] Fujian Med Univ, Sch Hlth, Fuzhou 350122, Peoples R China
[5] Fujian Tradit Med Univ, Fuzhou 350122, Peoples R China
[6] Fujian Med Univ, Affiliated Hosp 1, Natl Reg Med Ctr, Dept Rehabil Med, Binhai Campus, Fuzhou 350212, Peoples R China
关键词
Post-stroke cognitive impairment; Transcranial direct current stimulation; Virtual reality; Randomized controlled trial; Treatment; DIRECT-CURRENT STIMULATION; MENTAL-STATE-EXAMINATION; OUTCOMES;
D O I
10.1186/s12906-024-04658-0
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
BackgroundPost-stroke cognitive impairment (PSCI) not only increases patient mortality and disability, but also adversely affects motor function and the ability to perform routine daily activities. Current therapeutic approaches for, PSCI lack specificity, primarily relying on and medication and traditional cognitive therapy supplemented by a limited array of tools. Both transcranial direct current stimulation (tDCS) and virtual reality (VR) training have demonstrated efficacy in improving cognitive performance among PSCI patients. Previous findings across various conditions suggest that implementing a therapeutic protocol combining tDCS and VR (tDCS - VR) may yield superior in isolation. Despite this, to our knowledge, no clinical investigation combining tDCS and VR for PSCI rehabilitation has been conducted. Thus, the purpose of this study is to explore the effects of tDCS - VR on PSCI rehabilitation.MethodsThis 4-week, single-center randomized clinical trial protocol will recruit 200 patients who were randomly assigned to one of four groups: Group A (tDCS + VR), Group B (tDCS + sham VR), Group C (sham tDCS + VR), Group D (sham tDCS + sham VR). All four groups will receive conventional cognitive rehabilitation training. The primary outcome measurement utilizes the Mini-Mental State Examination (MMSE). Secondary outcome measures include the Montreal Cognitive Assessment, Frontal Assessment Battery, Clock Drawing Test, Digital Span Test, Logic Memory Test, and Modified Barthel Index. Additionally, S-YYZ-01 apparatus for diagnosis and treating language disorders assesses subjects' speech function. Pre- and post-four-week intervention assessments are conducted for all outcome measures. Functional near-infrared spectroscopy (fNIRS) is employed to observe changes in oxygenated hemoglobin (HbO), deoxy-hemoglobin (HbR), and total hemoglobin (HbT) in the cerebral cortex.DiscussionOur hypothesis posits that the tDCS - VR therapy, in opposed to individual tDCS or VR interventions, could enhance cognitive function, speech ability and daily living skills in PSCI patients while concurrently augmenting frontal cortical activity. This randomized study aims to provide a robust theoretical foundation supported by scientific evidence for the practical implementation of the tDCS - VR combination as a secure and efficient PSCI rehabilitation approach.Trial registrationChictr.org.cn Identifier: ChiCTR2300070580. Registered on 17th April 2023.
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页数:10
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