Abstract | Objective: Methods: In this single-arm, multi-center clinical trial, 61 patients with mild to moderate major depressive disorder were enrolled. tDCS treatment was delivered at the patient's home once a day, 5 to 7 times a week for 6 weeks, and each session lasted for 30 minutes. The primary outcome was a total Beck-Depression Inventory-II score, and no concurrent antidepressants were used. Results: The remission rates in both Full-Analysis (FA) (n = 61) and Per-Protocol (PP) (n = 43) groups were statistically significant (FA: 57.4% [0.44-0.70], PP: 62.8% [0.47-0.77]; percent [95% confidence interval]). The degree of depression- related symptoms was also significantly improved in 2, 4, and 6 weeks after the treatment when compared with baseline. There was no significant association between treatment compliance and remission rate in both FA and PP groups. Conclusion: These results suggest that acute treatment of patient-administered tDCS might be effective in improving the subjective feeling of depressive symptoms in mild to moderate major depressive disorder patients.
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Authors | Jihoon Oh, Sekye Jeon, Tae Hyon Ha, Woojae Myung, Seung-Hwan Lee, Young-Hoon Ko, Do Hoon Kim, Hwa-Young Lee, Jeong-Ho Chae |
Journal | Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology
(Clin Psychopharmacol Neurosci)
Vol. 21
Issue 2
Pg. 271-278
(May 30 2023)
ISSN: 1738-1088 [Print] Korea (South) |
PMID | 37119219
(Publication Type: Journal Article)
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