Home-based transcranial direct current stimulation treatment for major depressive disorder: a fully remote phase 2 randomized sham-controlled trial

经颅直流电刺激 重性抑郁障碍 随机对照试验 中止 背外侧前额叶皮质 医学 萧条(经济学) 安慰剂 临床终点 评定量表 心理学 物理疗法 前额叶皮质 内科学 刺激 精神科 认知 发展心理学 替代医学 病理 经济 宏观经济学
作者
Rachel D. Woodham,Sudhakar Selvaraj,Nahed Lajmi,Harriet Hobday,Gabrielle Sheehan,Ali-Reza Ghazi-Noori,Peter J. Lagerberg,Maheen Rizvi,Sarah Soonji Kwon,Paulette Orhii,David Maislin,Lucía Hernández,Rodrigo Machado‐Vieira,Jair C. Soares,Allan H. Young,Cynthia H.Y. Fu
出处
期刊:Nature Medicine [Nature Portfolio]
卷期号:31 (1): 87-95 被引量:79
标识
DOI:10.1038/s41591-024-03305-y
摘要

Abstract Transcranial direct current stimulation (tDCS) has been proposed as a new treatment in major depressive disorder (MDD). This is a fully remote, multisite, double-blind, placebo-controlled, randomized superiority trial of 10-week home-based tDCS in MDD. Participants were 18 years or older, with MDD in current depressive episode of at least moderate severity as measured using the Hamilton Depression Rating Scale (mean = 19.07 ± 2.73). A total of 174 participants (120 women, 54 men) were randomized to active ( n = 87, mean age = 37.09 ± 11.14 years) or sham ( n = 87, mean age = 38.32 ± 10.92 years) treatment. tDCS consisted of five sessions per week for 3 weeks then three sessions per week for 7 weeks in a 10-week trial, followed by a 10-week open-label phase. Each session lasted 30 min; the anode was placed over the left dorsolateral prefrontal cortex and the cathode over the right dorsolateral prefrontal cortex (active tDCS 2 mA and sham tDCS 0 mA, with brief ramp up and down to mimic active stimulation). As the primary outcome, depressive symptoms showed significant improvement when measured using the Hamilton Depression Rating Scale: active 9.41 ± 6.25 point improvement (10-week mean = 9.58 ± 6.02) and sham 7.14 ± 6.10 point improvement (10-week mean = 11.66 ± 5.96) (95% confidence interval = 0.51–4.01, P = 0.012). There were no differences in discontinuation rates. In summary, a 10-week home-based tDCS treatment with remote supervision in MDD showed high efficacy, acceptability and safety. ClinicalTrials.gov registration: NCT05202119
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