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Electroacupuncture for Major Depression: A Pilot Study

Electroacupuncture for Major Depression: A Pilot Study
电针治疗重度抑郁症:一项试点研究
批准号:
6680860
负责人:
BENOIT H MULSANT
金额:
$18.63万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-09-08 至 2005-05-31

项目摘要

项目成果

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中文摘要
翻译
描述(由申请人提供):重度抑郁症是一种常见的严重精神疾病。它与生活质量显著降低、显著功能障碍和因自杀或共病身体疾病导致的过早死亡相关。在过去的50年里,已经开发出了有效和安全的治疗重度抑郁症的方法,包括抗抑郁药物治疗,心理治疗和电休克治疗。然而,许多患有抑郁症的美国人要么不接受这些常规治疗之一,要么没有完成足够的治疗过程。越来越多的美国抑郁症患者选择接受补充和替代疗法。特别是针灸,越来越多地被用于治疗抑郁症,尽管只有有限的数据支持其安全性和有效性。拟议的试点研究建立在一组传统抗抑郁治疗研究人员和一组替代医学从业人员的互补专业知识的基础上。本研究将采用随机平行组设计,比较电针(EA)和假电针(SA)治疗重度抑郁症的安全性、有效性和耐受性。在15个月的时间内,60名患有轻度或中度严重程度(根据DSM-IV定义)的重度抑郁症的成人门诊患者将随机接受12次EA或SA治疗,为期6周。安全性和症状改善(采用汉密尔顿抑郁评定量表测量)将构成主要结局指标。耐受性和功能改善将构成次要结局指标。该试点项目产生的数据将用于支持进行一项大型多中心研究的可行性,并为该研究的设计提供信息,该研究比较了两种形式的针灸与传统治疗抑郁症的疗效。
英文摘要
DESCRIPTION (provided by applicant): Major depression is a common and serious mental illness. It is associated with a markedly lower quality of life, significant functional impairment, and premature death due to suicide or comorbid physical illness. Over the past 50 years, effective and safe treatments for major depression have been developed, including antidepressant pharmacotherapy, psychotherapy, and electroconvulsive therapy. However, many Americans who suffer from a depressive disorder either do not accept to receive one of these conventional treatments or do not complete an adequate course of treatment. A growing number of Americans with depression are choosing to be treated with complementary and alternative therapies. Acupuncture, in particular, is increasingly being used to treat depression even though only limited data support its safety and efficacy. The proposed pilot study builds upon the complementary expertise of a group of investigators of conventional antidepressant treatments and a group of practitioners of alternative medicine. It will use a randomized parallel-group design to compare the safety, efficacy, and tolerability of electroacupuncture (EA) and sham electroacupuncture (SA) for the treatment of major depression. Over a 15-month period, 60 adult outpatients with a major depressive disorder of mild or moderate severity (as defined by the DSM-IV) will be randomized to either 12 sessions of EA or SA to be provided over 6 weeks. Safety and symptomatic improvement (as measured with the Hamilton Rating Scale for Depression) will constitute the primary outcome measures. Tolerability and functional improvement will constitute secondary outcome measures. The data generated by this pilot project will be used to support the feasibility of conducting, and inform the design of, a large multicenter study comparing the efficacy of two forms of acupuncture with a conventional treatment for depression.
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