Japan Unified Protocol Clinical Trial for Depressive and Anxiety Disorders (JUNP study): study protocol for a randomized controlled trial

被引:7
作者
Ito, Masaya [1 ]
Okumura, Yasuyuki [2 ]
Horikoshi, Masaru [1 ]
Kato, Noriko [1 ]
Oe, Yuki [1 ]
Miyamae, Mitsuhiro [1 ]
Hirabayashi, Naotsugu [3 ]
Kanie, Ayako [3 ]
Nakagawa, Atsuo [4 ]
Ono, Yutaka [5 ]
机构
[1] Natl Ctr Neurol & Psychiat, Natl Ctr Cognit Behav Therapy & Res, Ogawa Higashi 4-1-1, Kodaira, Tokyo 1878511, Japan
[2] Assoc Hlth Econ Res & Social Insurance & Welf, Inst Hlth Econ & Policy, Tokyo, Japan
[3] Natl Ctr Neurol & Psychiat, Kodaira, Tokyo 1878511, Japan
[4] Keio Univ, Sch Med, Ctr Clin Res, Tokyo, Japan
[5] Ctr Dev Cognit Behav Therapy Training, Tokyo, Japan
来源
BMC PSYCHIATRY | 2016年 / 16卷
基金
日本学术振兴会;
关键词
Anxiety disorder; Depressive disorder; Emotion; Transdiagnostic; Unified protocol; Randomized controlled trial; COGNITIVE-BEHAVIORAL THERAPY; EMOTION-REGULATION SKILLS; TRANSDIAGNOSTIC TREATMENT; GENERALIZED ANXIETY; HOMEWORK COMPLIANCE; PANIC DISORDER; RATING-SCALE; PHARMACOLOGICAL-TREATMENT; ECONOMIC BURDEN; VALIDATION;
D O I
10.1186/s12888-016-0779-8
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: The unified protocol for the transdiagnostic treatment of emotional disorders is a promising treatment approach that could be applicable to a broad range of mental disorders, including depressive, anxiety, trauma-related, and obsessive-compulsive disorders. However, no randomized controlled trial has been conducted to verify the efficacy of the unified protocol on the heterogeneous clinical population with depressive and anxiety disorders. Methods/design: The trial was designed as a single-center, assessor-blinded, randomized, 20-week, parallel-group superiority study in order to compare the efficacy of the combination of unified protocol and treatment-as-usual versus waiting-list with treatment-as-usual for patients with depressive and/or anxiety disorders. The primary outcome was depression at 21 weeks, assessed by the 17-item version of the GRID-Hamilton Rating Scale for Depression. Estimated minimum sample size was 27 participants in each group. We will also examine the treatment mechanisms, treatment processes, and neuropsychological correlates. Discussion: The results of this study will clarify the efficacy of the unified protocol for depressive and anxiety disorders, and the treatment mechanism, process, and neurological correlates for the effectiveness of the unified protocol. If its efficacy can be confirmed, the unified protocol may be of high clinical value for Japan, a country in which cognitive behavioral treatment has not yet been widely adopted.
引用
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页数:15
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