Kane John M, Schooler Nina R, Marcy Patricia, Correll Christoph U, Brunette Mary F, Mueser Kim T, Rosenheck Robert A, Addington Jean, Estroff Sue E, Robinson James, Penn David L, Robinson Delbert G
Department of Psychiatry, The Zucker Hillside Hospital, 75-59 263rd St, Kaufmann Bldg, Ste 103, Glen Oaks, NY 11004
J Clin Psychiatry. 2015 Mar;76(3):240-6. doi: 10.4088/JCP.14m09289.
The premise of the National Institute of Mental Health Recovery After an Initial Schizophrenia Episode Early Treatment Program (RAISE-ETP) is to combine state-of-the-art pharmacologic and psychosocial treatments delivered by a well-trained, multidisciplinary team in order to significantly improve the functional outcome and quality of life for first-episode psychosis patients. The study is being conducted in non-academic (ie, real-world) treatment settings, using primarily extant reimbursement mechanisms.
We developed a treatment model and training program based on extensive literature review and expert consultation. Our primary aim is to compare the experimental intervention to "usual care" on quality of life. Secondary aims include comparisons on remission, recovery, and cost-effectiveness. Patients 15-40 years old with a first episode of schizophrenia, schizoaffective disorder, schizophreniform disorder, psychotic disorder not otherwise specified, or brief psychotic disorder according to DSM-IV and no more than 6 months of treatment with antipsychotic medications were eligible. Patients are followed for a minimum of 2 years, with major assessments conducted by blinded, centralized raters using live, 2-way video. We selected 34 clinical sites in 21 states and utilized cluster randomization to assign 17 sites to the experimental treatment and 17 to usual care. Enrollment began in July 2010 and ended in July 2012 with 404 subjects. The results of the trial will be published separately. The goal of the article is to present both the overall development of the intervention and the design of the clinical trial to evaluate its effectiveness.
We believe that we have succeeded in both designing a multimodal treatment intervention that can be delivered in real-world clinical settings and implementing a controlled clinical trial that can provide the necessary outcome data to determine its impact on the trajectory of early phase schizophrenia.
ClinicalTrials.gov identifier: NCT01321177.
美国国立精神卫生研究所首发精神分裂症发作后早期治疗项目(RAISE - ETP)的前提是,由训练有素的多学科团队提供最先进的药物和心理社会治疗,以显著改善首发精神病患者的功能结局和生活质量。该研究在非学术(即现实世界)治疗环境中进行,主要使用现有的报销机制。
我们基于广泛的文献综述和专家咨询,开发了一种治疗模式和培训项目。我们的主要目的是比较实验性干预与“常规治疗”对生活质量的影响。次要目的包括比较缓解率、康复情况和成本效益。符合条件的患者年龄在15至40岁之间,根据《精神疾病诊断与统计手册》第四版(DSM - Ⅳ)诊断为首发精神分裂症、分裂情感性障碍、精神分裂症样障碍、未另行规定的精神病性障碍或短暂精神病性障碍,且使用抗精神病药物治疗不超过6个月。对患者进行至少2年的随访,主要评估由不知情的集中评估人员通过实时双向视频进行。我们在21个州选择了34个临床地点,并采用整群随机化方法将17个地点分配到实验性治疗组,17个地点分配到常规治疗组。招募工作于2010年7月开始,2012年7月结束,共纳入404名受试者。该试验的结果将另行发表。本文的目的是介绍干预措施的整体开发情况以及评估其有效性的临床试验设计。
我们相信,我们成功设计了一种可在现实世界临床环境中实施的多模式治疗干预措施,并开展了一项对照临床试验,该试验能够提供必要的结局数据,以确定其对早期精神分裂症病程的影响。
ClinicalTrials.gov标识符:NCT01321177。