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

Primary Purpose

Major Depressive Disorder

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors)
Treatment as Usual
SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) Combined with Magnetic Stimulations
Sponsored by
Shanghai Mental Health Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depressive Disorder

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. 18-60 years old;
  2. Meeting with the criteria of major depressive disorder in the Diagnostic and Statistical Manual of Mental Disorders (DSM)-5;
  3. Scored 20 or higher on the Hamilton's Depression Scale with 24 items (HAMD-24);
  4. With enough audio-visual ability and comprehensive ability to accomplish the visits;
  5. No medication or washout period of at least 2 weeks
  6. Scored less than 14 on the Hypomania Symptom Checklist-32 (HCL-32);

Exclusion Criteria:

  1. 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;
  2. Previous mania or hypomania episodes;
  3. Female patients who are pregnant, planning to be pregnant or breastfeeding;
  4. Current high suicide risk (e.g. 3rd item of HAMD-24 scored≥3(suicidality));
  5. Had ECT, MECT or rTMS in the past 6 months;
  6. Experienced a history of dependence on psychoactive substances, organic mental disorders, personality disorders, mental retardation, neurodegenerative diseases, brain trauma and cerebrovascular diseases.

Sites / Locations

  • Huashan Hospital, Fudan University
  • Med-X Research Institute of Shanghai Jiao Tong University
  • Renji Hospital of Shanghai Jiao Tong University School of Medicine
  • Shanghai Tenth People's Hospital, Tongji University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

MDD with melancholic features

MDD with atypical features

MDD with anxious distress

MDD (overall)

Arm Description

Outcomes

Primary Outcome Measures

remission of acute phase
scored 7 or lower on the Hamilton's Depression Scale with 24 items

Secondary Outcome Measures

Full Information

First Posted
August 24, 2020
Last Updated
August 24, 2020
Sponsor
Shanghai Mental Health Center
Collaborators
RenJi Hospital, Shanghai 10th People's Hospital, Huashan Hospital, Shanghai Jiao Tong University School of Medicine, Nanjing Medical University, Zhejiang University
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1. Study Identification

Unique Protocol Identification Number
NCT04528628
Brief Title
Optimization of Diagnosis and Treatment of Depression Based on Multidimensional Clinical Assessment Classification
Official Title
Optimization of Diagnosis and Treatment of Depression Based on Multidimensional Clinical Assessment Classification
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 2020 (Anticipated)
Primary Completion Date
September 2022 (Anticipated)
Study Completion Date
September 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Mental Health Center
Collaborators
RenJi Hospital, Shanghai 10th People's Hospital, Huashan Hospital, Shanghai Jiao Tong University School of Medicine, Nanjing Medical University, Zhejiang University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
960 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MDD with melancholic features
Arm Type
Experimental
Arm Title
MDD with atypical features
Arm Type
Experimental
Arm Title
MDD with anxious distress
Arm Type
Experimental
Arm Title
MDD (overall)
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors)
Intervention Description
Patients will be treated with one kind of selective serotonin reuptake inhibitors/ serotonin and norepinephrine reuptake inhibitors. Dose is titrated to the minimum effective dose within 2 weeks. Benzodiazepines can be used for a short period lasting no more than 2 weeks.
Intervention Type
Drug
Intervention Name(s)
Treatment as Usual
Intervention Description
The research doctor discusses the treatment plan with the patient, and therapies and drugs are not limited.
Intervention Type
Combination Product
Intervention Name(s)
SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) Combined with Magnetic Stimulations
Intervention Description
Drug therapies are the same as the SSRIs/SNRIs monotherapy group. Patients will randomly receive one kind of magnetic stimulations including repetitive transcranial magnetic stimulation (rTMS), continuous theta burst stimulation(cTBS) and intermittent theta burst stimulation (iTBS) at a ratio of 1:1:1.
Primary Outcome Measure Information:
Title
remission of acute phase
Description
scored 7 or lower on the Hamilton's Depression Scale with 24 items
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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); Exclusion Criteria: 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Daihui Peng, MD. PhD.
Phone
18017311136
Email
pdhsh@126.com
Facility Information:
Facility Name
Huashan Hospital, Fudan University
City
Shanghai
State/Province
Shanghai
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yiyun Cai
Facility Name
Med-X Research Institute of Shanghai Jiao Tong University
City
Shanghai
State/Province
Shanghai
Country
China
Facility Name
Renji Hospital of Shanghai Jiao Tong University School of Medicine
City
Shanghai
State/Province
Shanghai
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yanli Luo
Facility Name
Shanghai Tenth People's Hospital, Tongji University
City
Shanghai
State/Province
Shanghai
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yuan Shen

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

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

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