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.
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