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临床试验/NCT01558154
NCT01558154Unknown不适用

Comparison of Treatment Effect of Chinese Medicine and Western Medicine on Depression in China and America

Guang'anmen Hospital of China Academy of Chinese Medical Sciences1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2012年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
160
试验地点
1
主要终点
psychological questionnaires

研究概览

简要总结

Comparison of different assessment methods to evaluate the treatment efficacy of Chinese medicine on minor and mild depression.

详细描述

Significant differences show on the evaluation of treatment efficacy of Chinese medicine on depression in China and America. Choose minor and mild depression patients as trials. One hundred and sixty trials will be included and randomly divided into Chinese medicine group (n=40), acupuncture group (n=40), traditional Chinese medicine psychology group (n=40) and physical treatment group (n=40). Time points of assessment are before treatment, 1 week, 2 weeks, 4weeks, 6 weeks and 12 weeks post treatment.The assessment tools are series of psychological questionnaires. And study the mechanism of treatment efficacy assessment variances by different methods.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
None

入排标准

年龄范围
16 Years 至 70 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • According with ICD-10 criteria of depression;
  • Age 16-70;
  • Antidepressant and other Psychiatric drugs have not been had two weeks before the trial, or the drugs above had been used but have cleaning period of two weeks;
  • Level of education is higher than junior middle school;
  • Course of disease is more than two weeks;
  • Volunteer to join and Signed the informed consent

排除标准

  • Pregnancy or lactation;
  • Severe depression or have serious suicidal tendencies
  • long distance or other causes who can not adherence to treatment

研究组 & 干预措施

Chinese herb

Experimental

Chinese herbs special for depression

干预措施: Chinese herbs (Drug)

acupuncture

Experimental

干预措施: acupuncture (Procedure)

Psychotherapy

Experimental

干预措施: Psychotherapy (Other)

physiotherapy

Experimental

干预措施: Transcranial magnetic stimulation (Device)

结局指标

主要结局

psychological questionnaires

时间窗: 12 weeks post treatment.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Xue Yan

Psychology Department

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

研究点 (1)

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