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临床试验/NCT00788970
NCT00788970Unknown不适用

Shiatsu Adjuvant Therapy And Placebo For Schizophrenia:a Double Blind Study

Herzog Hospital2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2009年1月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
150
试验地点
2
主要终点
Brief Psychiatric Rating Scale (BPRS)

研究概览

简要总结

In the current study we will study the effect of adding acupressure (shiatsu) to conventional therapy in treating individuals with schizophrenia.

详细描述

Acupressure, also known as shiatsu, is a holistic form of medicine originating in Japan but now widely practiced throughout the world. The theory is based on Traditional Chinese Medicine (TCM), which sees meridians of life force (chi) running through the body, and aims to optimize health through manipulating the body into maximal alignment.

We are proposing a randomized double-blind placebo-controlled trial to examine the efficacy of acupressure as adjuvant therapy added to antipsychotics in the treatment of patients with schizophrenia.

The goals of this study are twofold:

  1. To assess through the highest standards of empirical research whether acupressure can benefit patients with schizophrenia.
  2. To furnish data relevant to the possible physiological mechanisms by which acupressure may produce a therapeutic effect.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • DSM-IV diagnosis of schizophrenia or schizoaffective disorder
  • Ages 18 and over
  • Clinical status stable, as reflected by changes in Brief Psychiatric Rating Scale (BPRS) (Overall & Gorham, 1961) of less than 20% during a one month period prior to randomization, and at least one month of drug treatment without change of anti-psychotic drug or dosage.
  • Ability to cooperate with 40-minute sessions

排除标准

  • Unstable general medical conditions
  • Active bone fracture or other orthopedic problem
  • Skin condition that renders treatment unsafe or painful
  • Active infection in skin or soft tissues, such as cellulitis
  • Solid tissue malignancy

结局指标

主要结局

Brief Psychiatric Rating Scale (BPRS)

时间窗: 16 weeks

次要结局

未报告次要终点

研究者

发起方
Herzog Hospital
申办方类型
Other

研究点 (2)

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