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临床试验/ITMCTR2000003218
ITMCTR2000003218招募中未知

Research on health state intervention by active and passive ways and management techniques based on the combination of traditional Chinese medicine constitution (subtopic 3) : clinical evaluation of intervention techniques for subthreshold depression, insomnia and mild cognitive impairment

Beijing University of Chinese Medicine0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
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 65(—)
性别
All

入选标准

  • 1. Patients who meet the diagnostic criteria of depression under the threshold of Western medicine;
  • Diagnosis standard of subthreshold depression: it has symptoms of depression, but fails to meet the symptom indicators required for diagnosis of depression (more than 5 of 9 items: loss of interest, no pleasure; energy loss or fatigue; psychomotor retardation or agitation; low self-evaluation, self blame, or guilt; difficulty in association or reduction of conscious thinking ability; recurrent thoughts of dying or having self Killing and self injuring behaviors; sleep disorders, such as insomnia, early wake-up, or excessive sleep; loss of appetite or weight; hyposexual desire) or course indicators (duration greater than 2 weeks).
  • 2. The patients with CES-D score >= 16;
  • 3. Hamilton Depression Scale (HAMD-17) score: 7 points <= HAMD total score < 17 points;
  • 4. The patients with qi stagnation as the main constitution were classified and judged by the constitution of traditional Chinese medicine;
  • 5. Patients aged over 18 and under 65, regardless of gender;
  • 6. Patients who can independently complete the questionnaire, use the app, have informed consent and voluntarily fill in the questionnaire;
  • Only those who meet the above six criteria can be selected into the research group.

排除标准

  • 1. Patients with clinically confirmed depression, previous mental illness or organic mental disorder;
  • 2. Patients with serious liver and kidney function damage, serious heart rate disorder or cardiac insufficiency;
  • 3. Pregnancy, lactation and objects with pregnancy plan;
  • 4. Patients with depressive episode caused by psychoactive substance and non addictive substance;
  • 5. Patients who used other drugs or therapies to treat depression at the same time during the trial;
  • 6. Known targets of drinking or substance dependence;
  • 7. Patients with strong suicide attempt or behavior;
  • 8. Patients who are participating in other clinical trials;
  • 9. Those who fail to treat according to the specified requirements, fail to judge the curative effect or incomplete data that affect the judgment of curative effect or safety;
  • 10. Patients who had received antidepressant treatment within one week before the trial.
  • Those with one of the above items will not be included in the test.

研究者

发起方
Beijing University of Chinese Medicine

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