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Pragmatic randomised controlled trial of group psychoeducation versus group support in the maintenance of bipolar disorder

机译:团体心理教育与团体支持在维持躁郁症中的实用随机对照试验

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Background Non-didactically delivered curriculum based group psychoeducation has been shown to be more effective than both group support in a specialist mood disorder centre in Spain (with effects lasting up to five years), and treatment as usual in Australia. It is unclear whether the specific content and form of group psychoeducation is effective or the chance to meet and work collaboratively with other peers. The main objective of this trial is to determine whether curriculum based group psychoeducation is more clinically and cost effective than unstructured peer group support. Methods/design Single blind two centre cluster randomised controlled trial of 21 sessions group psychoeducation versus 21 sessions group peer support in adults with bipolar 1 or 2 disorder, not in current episode but relapsed in the previous two years. Individual randomisation is to either group at each site. The groups are carefully matched for the number and type of therapists, length and frequency of the interventions and overall aim of the groups but differ in content and style of delivery. The primary outcome is time to next bipolar episode with measures of the therapeutic process, barriers and drivers to the effective delivery of the interventions and economic analysis. Follow up is for 96 weeks after randomisation. Discussion The trial has features of both an efficacy and an effectiveness trial design. For generalisability in England it is set in routine public mental health practice with a high degree of expert patient involvement. Trial Registration ISRCTN62761948 Funding National Institute for Health Research, England.
机译:背景技术在西班牙一个专业的情绪障碍中心(效果持续长达五年)和在澳大利亚照常进行治疗,事实证明,非基于课程的基于小组心理教育的课程要比小组支持更为有效。目前尚不清楚小组心理教育的具体内容和形式是否有效,或者是否有机会与其他同龄人会面和合作。该试验的主要目的是确定基于课程的小组心理教育是否比非结构化的同伴小组支持更具临床价值和成本效益。方法/设计对患有双相性1或2型躁郁症的成年人进行了21课时小组心理教育与21课时小组同伴支持的单盲,两中心集群随机对照试验,但不是当前发作,而是在前两年复发。在每个站点将随机分组到任一组。小组根据治疗师的数量和类型,干预的时间和频率以及小组的总体目标进行了仔细匹配,但内容和交付方式有所不同。主要结果是下一次出现双相情感障碍的时间,包括治疗过程的指标,有效实施干预措施和经济分析的障碍和驱动因素。随机分组后随访96周。讨论该试验具有有效性和有效性试验设计的特征。为了在英格兰具有通用性,在常规的公共精神卫生实践中设置了高度的专业患者参与度。试用注册号ISRCTN62761948,英国国立卫生研究院。

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