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The efficacy of transcranial alternating current stimulation for treating post-stroke depression: Study Protocol Clinical Trial (SPIRIT Compliant).

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机构: [a]Department of Neurology, Xuanwu Hospital, Capital Medical University, [b]Beijing Key Laboratory of Neuromodulation, [c]Center of Epilepsy, Beijing Institute for Brain Disorders, Capital Medical University, [d]Department of Neurology, Beijing Puren Hospital, [e]Medical Research & Biometrics Centre, National Centre for Cardiovascular Diseases Cardiovascular, [f]Andrius Baskys, Graduate College of Biomedical Sciences, Western University of Health Sciences, Pomona, CA, [g]Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, TX
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The treatment of post-stroke depression (PSD) with anti-depressant drugs is partly practical. Transcranial alternating current stimulation (tACS) offers the potential for a novel treatment modality for adult patients with PSD. In this study, we will assess the efficacy and safety of tACS for treating PSD and explore its effect on gamma and beta-oscillations involving in emotional regulation. The prospective study is an 8-week, double-blind, randomized, placebo-controlled trial. Seventy eligible participants with mild to moderate PSD aged between 18 years and 70 years will be recruited and randomly assigned to either active tACS intervention group or sham group. Daily 40-minute, 77.5-Hz, 15-mA sessions of active or sham tACS targeting the forehead and both mastoid areas on weekdays for 4 consecutive weeks (week 4), and an additional 4-week observational period (week 8) will be followed up. The primary outcome is the proportion of participants having an improvement at week 8 according to the Hamilton Depression Rating Scale 17-Item (HAMD-17) score, including the proportion of participants having a decrease of ≥ 50% in HAMD-17 score or clinical recovery (HAMD-17 score ≤ 7). Secondary outcomes include neurological function, independence level, activities of daily living, disease severity, anxiety, and cognitive function. The exploratory outcomes are gamma and beta-oscillations assessed at baseline, week 4, and week 8. Data will be analyzed by logistical regression analyses and mixed-effects models. The study will be the first randomized controlled trial to evaluate the efficacy and safety of tACS at a 77.5-Hz frequency and 15-mA current in reducing depressive severity in patients with PSD. The results of the study will present a base for future studies on the tACS in PSD and its possible mechanism. NCT03903068, pre-results.

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出版当年[2019]版:
大类 | 4 区 医学
小类 | 3 区 医学:内科
最新[2023]版:
大类 | 4 区 医学
小类 | 4 区 医学:内科
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出版当年[2018]版:
Q2 MEDICINE, GENERAL & INTERNAL
最新[2023]版:
Q2 MEDICINE, GENERAL & INTERNAL

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第一作者机构: [a]Department of Neurology, Xuanwu Hospital, Capital Medical University, [b]Beijing Key Laboratory of Neuromodulation, [c]Center of Epilepsy, Beijing Institute for Brain Disorders, Capital Medical University, [*1]Haiqing Song, Division of Neuropsychiatry and Psychosomatics, Department of Neurology of Xuanwu Hospital, Capital Medical University, No.45, Changchun Street, Xicheng District, Beijing 100053, China
通讯作者:
通讯机构: [*1]Haiqing Song, Division of Neuropsychiatry and Psychosomatics, Department of Neurology of Xuanwu Hospital, Capital Medical University, No.45, Changchun Street, Xicheng District, Beijing 100053, China
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