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临床试验/NCT02942251
NCT02942251Unknown不适用

The Study of Relapse Predicting Model for First Episode Depression: Big Data Analysis Based on Clinical Features and Immunochemistry

Shanghai Mental Health Center0 个研究点目标入组 300 人开始时间: 2016年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
300
主要终点
HAM-D total score

研究概览

简要总结

Major depressive depression(MDD) is an severe public mental disorders. The purpose of current study is using big data analysis based on clinical features and immunochemistry to investigate and establish an relapse predict model for patients with first episode MDD.

详细描述

Major depressive depression(MDD) is an severe public mental disorders. The purpose of current study is using big data analysis based on clinical features and immunochemistry to investigate and establish an relapse predict model for patients with first episode MDD.

This study includes two steps. Step 1: Big data analysis based on the clinical features and immunochemical figures of 30000 patients with first episode MDD will be conducted to construct a relapse predict model.

Step 2: 300 patients with first episode MDD will be recruited in this step. Physicians prefer to give corresponding treatment recommendation based on the predictive factors to verify this relapse model.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Age from 18 to 65 years old;
  • •Han Chinese;
  • •Outpatient and inpatient patients;
  • •Patients met Diagnostic and Statistical Manual of Mental Disorders(DSM-IV-TR) criteria of bipolar I or II disorder, currently depressed, ascertained with the Mini International Neuropsychiatric Interview (MINI)
  • •Hamilton Depression Scale(HAM-D) total score≥17, HAM-D item 1 (depressed mood) score≥2, and Young Mania Rating Scale(YMRS) total score≤10 at baseline;
  • •Written informed consent was given;
  • •Junior high school education and above, with enough audio-visual ability to accomplish the visits;
  • •Normally resident in one country and had a residential address, able to follow-up.

排除标准

  • •Bipolar disorder rapid cycling or mixed episode;
  • •Experienced DSM-IV-TR axis I disorders in the 6 months prior to randomization;
  • •Severe personality disorder, metal retardation, anorexia/bulimia nervosa;
  • •Actively suicide ascertained by research psychiatrist or HAM-D item 3 score≥3(suicidality);
  • •Female patients who were pregnant, planning to be pregnant or breast feeding;
  • •Severe medical or neurological problems.

研究组 & 干预措施

Clinical features and medication

Experimental

A group patients with significant high risk of clinical features and medications.

干预措施: Clinical features and medication (Other)

Psycho-social

Experimental

A group patients with significant high risk of psycho-social problems.

干预措施: Psycho-social (Other)

immunology

Experimental

A group patients with significant high risk of immune disturbance.

干预措施: immunology (Other)

Laboratory abnormality

Experimental

A group patients with significant high risk of Laboratory abnormalities.

干预措施: Laboratory abnormality (Other)

Comorbidity

Experimental

A group patients with physical or mental disorders comorbidities.

干预措施: Comorbidity (Other)

Treatment as usual

Experimental

Control group.

干预措施: Treatment as usual (Other)

结局指标

主要结局

HAM-D total score

时间窗: 12 weeks

The change from baseline to end of study (EOS) in HAM-D total score

次要结局

  • Time to relapse(12 months)

研究者

申办方类型
Other
责任方
Sponsor

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