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临床试验/ITMCTR2000003083
ITMCTR2000003083尚未招募1 期

Effectiveness of Electro-Acupuncture on treating MDD: a Randomized Controlled Trial

Shanghai Seventh People's Hospital, Shanghai University of TCM0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional study

入排标准

年龄范围
18 至 75(—)
性别
All

入选标准

  • Patients with MDD who meet the following criteria will be included:
  • 1. Between 18 and 75 years of age with no gender-based restriction;
  • 2. Fulfilling the diagnostic criteria of Diagnostic and Statistical Manual of Mental Disorders version 5 (DSM V) for major depressive disorder;
  • 3. A Hamilton Rating Scale for Depression (HDRS-17) score with a range between 17 to 24 (24 > HDRS-17 >= 17);
  • 4. Non-aphasic and without severe cognitive disorders, with a Mini-Mental State Examination (MMSE) score (H) greater than 17 (MMSE > 17);
  • 5. Keenness to participate in the trial and provide written informed consent.

排除标准

  • Subjects reporting any of the following criteria will be excluded:
  • 1. History or current presence of neuropsychiatric diseases other than depression
  • 2. Candidates at a high risk of attempting suicide (a score of more than 2 points on the third question (Suicide) of the HDRS-17
  • 3. People who, prior to the date of screening:
  • Have taken antidepressants or any psychotropic drugs;
  • Have undergone psychotherapy or Cognitive Behavioral Therapy (CBT);
  • Received any kind of therapeutic interventions related to either Western medical practice or
  • Traditional Chinese Medicine to alleviate the symptoms of MDD.
  • 4. Pregnant, lactating, or planning to become pregnant women;
  • 5. Subjects who have acute inflammation at the planned acupuncture site on the body or any other contraindication to acupuncture;
  • 6. Candidates afraid of needles in general and reluctant to receive acupuncture in particular;
  • 7. Patients with bleeding tendency, severe physical disability or other chronic disorders (e.g: chronic alcoholism, drug abuse);
  • 8. Subject who have already taken part in previous clinical trials where EA treatment was used.

研究者

发起方
Shanghai Seventh People's Hospital, Shanghai University of TCM

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