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临床试验/NCT04528628
NCT04528628Unknown不适用

Optimization of Diagnosis and Treatment of Depression Based on Multidimensional Clinical Assessment Classification

Shanghai Mental Health Center4 个研究点 分布在 1 个国家目标入组 960 人开始时间: 2020年10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
960
试验地点
4
主要终点
remission of acute phase

研究概览

简要总结

Major depressive disorder (MDD) characterized by high prevalence, high recurrence rate and high disability rate is a mental illness with the heaviest burden and has become a major public health issue in China and the world. Great challenges in diagnosis and treatment of depression consist of the complicated pathogenesis, a lack of objective diagnostic criteria, unsatisfactory treatment outcomes and poor treatment compliance. The previous studies of our research team showed that depression is affected by multiple factors. We could explore important markers for the diagnosis, treatment and prediction of treatment efficacy in depressed patients' data collected from different dimensions including immunometabolism, brain electrophysiology, brain structure and functional neural circuits, neuropsychology and psychophysiology. Our completed studies in the National Science and Technology Support Program and National Key Research and Development (R&D) Program of the 12th and 13th Five-Year Plan in China found that treatment designed for specific clinical subtypes can improve the treatment effect, and meanwhile, the application of electronic-measurement based care (e-MBC) combined with smart mobile terminals can effectively provide whole-course medical management for patients, improve patient compliance and increase the efficacy of clinical diagnosis and treatment. However, due to disease diagnosis based on clinical symptomatology without subtype distinction and lack of multi-scale biological data mining, multidimensional assessment and deep integration, the results of most previous studies can hardly be used in clinical practice. Therefore, there is a strong urge to carry out a systematic research in which multidimensional evaluation of clinical characteristics and a large scale of data collection and mining are needed to form clinical diagnosis and optimal treatment regimens for depression subtypes. To achieve the goal, patients with depression will be our research subject in this study. First, on the basis of the previous cohort study and the whole-course e-MBC, patients' data of movement, respiratory rate, heart rate and sleep will be further collected. With the help of artificial intelligence (AI) technology such as deep machine learning, the data integrated with EEG imaging and specific immunometabolic markers in blood will be analyzed with clinical characteristics. The model of diagnosis and classification will be established based on multidimensional clinical assessment and verified. Second, through a prospective multicenter randomized controlled trial, optimal treatment regimens for different depression subtypes and individualized magnetic stimulation physical intervention technology navigated by AI will be explored so as to establish a predictive model of curative effect. Finally, long-term follow-up and its regular data collection can be completed on the patient diagnosis and treatment platform which is linked to the e-MBC. Thus, a stable clinical cohort and an advanced database containing multidimensional information of depression will be set up. The whole course e-MBC management platform will be optimized and promoted to improve patient compliance, treatment efficiency and prognosis. This study can provide evidence for precise diagnosis and classification of depression and optimal treatment regimens for different subtypes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 18-60 years old;
  • Meeting with the criteria of major depressive disorder in the Diagnostic and Statistical Manual of Mental Disorders (DSM)-5;
  • Scored 20 or higher on the Hamilton's Depression Scale with 24 items (HAMD-24);
  • With enough audio-visual ability and comprehensive ability to accomplish the visits;
  • No medication or washout period of at least 2 weeks
  • Scored less than 14 on the Hypomania Symptom Checklist-32 (HCL-32);

排除标准

  • Existing serious and active physical diseases that may interfere with treatment (abnormal indicators> 2 times the normal value), or there is a pharmacological conflict between the current medical medication and the study drug;
  • Previous mania or hypomania episodes;
  • Female patients who are pregnant, planning to be pregnant or breastfeeding;
  • Current high suicide risk (e.g. 3rd item of HAMD-24 scored≥3(suicidality));
  • Had ECT, MECT or rTMS in the past 6 months;
  • Experienced a history of dependence on psychoactive substances, organic mental disorders, personality disorders, mental retardation, neurodegenerative diseases, brain trauma and cerebrovascular diseases.

研究组 & 干预措施

MDD with melancholic features

Experimental

干预措施: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) (Drug)

MDD with melancholic features

Experimental

干预措施: Treatment as Usual (Drug)

MDD with melancholic features

Experimental

干预措施: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) Combined with Magnetic Stimulations (Combination Product)

MDD with atypical features

Experimental

干预措施: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) (Drug)

MDD with atypical features

Experimental

干预措施: Treatment as Usual (Drug)

MDD with atypical features

Experimental

干预措施: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) Combined with Magnetic Stimulations (Combination Product)

MDD with anxious distress

Experimental

干预措施: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) (Drug)

MDD with anxious distress

Experimental

干预措施: Treatment as Usual (Drug)

MDD with anxious distress

Experimental

干预措施: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) Combined with Magnetic Stimulations (Combination Product)

MDD (overall)

Experimental

干预措施: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) (Drug)

MDD (overall)

Experimental

干预措施: Treatment as Usual (Drug)

MDD (overall)

Experimental

干预措施: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) Combined with Magnetic Stimulations (Combination Product)

结局指标

主要结局

remission of acute phase

时间窗: 12 weeks

scored 7 or lower on the Hamilton's Depression Scale with 24 items

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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