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<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">CNR</journal-id><journal-title-group><journal-title>Clinical Neuroscience Research</journal-title></journal-title-group><issn>3083-4899</issn><eissn>2981-8133</eissn><publisher><publisher-name>Bio-Byword Scientific Publishing Pty. Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.26689/cnr.v1i3.5968</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Safety and Effectiveness Analysis of Accelerated rTMS in Treating Patients with Post-Stroke Depression</title><url>https://artdesignp.com/journal/CNR/1/3/10.26689/cnr.v1i3.5968</url><author>LiShanyou</author><pub-date pub-type="publication-year"><year>2023</year></pub-date><volume>1</volume><issue>3</issue><history><date date-type="pub"><published-time>2023-12-26</published-time></date></history><abstract>Objective: To investigate and analyze the safety and effectiveness of accelerated repetitive transcranial magnetic&amp;nbsp;stimulation (arTMS) in the treatment of post-stroke depression. Methods: 70 patients with post-stroke depression from&amp;nbsp;the Department of Psychiatry were selected as research subjects for this study. The study period was from June 2022 to&amp;nbsp;June 2023. The patients were divided into the arTMS group and the general treatment group, with 35 cases in each group.&amp;nbsp;The arTMS group received arTMS and the general treatment group received conventional treatment. The overall efficacy,&amp;nbsp;related scores, sleep level, quality of life, and side effects of treatment were compared between the groups. Results: The&amp;nbsp;overall efficacy of aRTMS was ideal. Besides, there were no significant differences in the scores of relevant scores between&amp;nbsp;the two groups before treatment; after treatment, the arTMS demonstrated a greater decrease in the scores. Besides, the&amp;nbsp;sleep quality of the patients in the arTMS group was better (P &amp;lt; 0.05). Furthermore, the quality of life of the arTMS group&amp;nbsp;was significantly improved (P &amp;lt; 0.05). 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