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Efficacy of the unified protocol for transdiagnostic cognitive-behavioral treatment for depressive and anxiety disorders: a randomized controlled trial

焦虑 临床全球印象 哈姆德 萧条(经济学) 随机对照试验 汉密尔顿焦虑量表 心理学 临床心理学 临床试验 精神科 内科学 医学
作者
Masaya Ito,Masaru Horikoshi,Noriko Kato,Yuki Oe,Hiroko Fujisato,Keiko Yamaguchi,Shun Nakajima,Mitsuhiro Miyamae,Ayaka Toyota,Yasuyuki Okumura,Yoshitake Takebayashi
出处
期刊:Psychological Medicine [Cambridge University Press]
卷期号:: 1-12
标识
DOI:10.1017/s0033291721005067
摘要

Abstract Background The efficacy of the unified protocol of the transdiagnostic treatment for emotional disorders (UP) has been poorly studied in patients with depressive disorders. This study aimed to examine the efficacy of UP for improving depressive symptoms in patients with depressive and/or anxiety-related disorders. Methods This assessor-blinded, randomized, 20-week, parallel-group, superiority study compared the efficacy of the UP with treatment-as-usual (UP-TAU) v. wait-list with treatment-as-usual (WL-TAU). Patients diagnosed with depressive and/or anxiety disorders and with depressive symptoms participated. The primary outcome was depressive symptoms assessed by GRID-Hamilton depression rating scale (GRID-HAMD) at 21 weeks. The secondary outcomes included assessor-rated anxiety symptoms, severity and improvement of clinical global impression, responder and remission status, and loss of principal diagnosis. Results In total, 104 patients participated and were subjected to intention-to-treat analysis [mean age = 37.4, s.d. = 11.5, 63 female (61%), 54 (51.9%) with a principal diagnosis of depressive disorders]. The mean GRID-HAMD scores in the UP-TAU and WL-TAU groups were 16.15 ( s.d. = 4.90) and 17.06 ( s.d. = 6.46) at baseline and 12.14 ( s.d. = 5.47) and 17.34 ( s.d. = 5.78) at 21 weeks, with a significant adjusted mean change difference of −3.99 (95% CI −6.10 to −1.87). Patients in the UP-TAU group showed significant superiority in anxiety and clinical global impressions. The improvement in the UP-TAU group was maintained in all outcomes at 43 weeks. No serious adverse events were observed in the UP-TAU group. Conclusions The UP is an effective approach for patients with depressive and/or anxiety disorders.

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