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Multi-Dimensional Diagnosis,Individualized Therapy,and Management Technique for Major Depressive Disorder:Based on Clinical and Pathological Characteristics (STEP-MDD)

Primary Purpose

Depressive Disorder

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Fluoxetine
fluoxetine + cognitive-behavioral treatment(CBT)
fluoxetine + Amfebutamone
physical treatment+fluoxetine+amfebutamone
Fluvoxamine
Lithium+fluvoxamine
fluvoxamine + lithium + physical therapy
Cognitive behavior treatment +fluvoxamine
Mirtazapine/SNRIs
mirtazapine+ Cognitive behavior treatment
mirtazapine + SNRIs
mirtazapine + SNRIs + physical therapy
TAU(treat as usual)
Sponsored by
Shanghai Mental Health Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depressive Disorder focused on measuring depressive disorder, multi-dimensional diagnosis technique, individualized therapy, management technique, e-MBC, MBC

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • aged 18-65 years;
  • clinical diagnosis of major depressive disorder;
  • 17-Hamilton Depression Scale>20;
  • 14-Hamilton Anxiety Scale score<7;
  • outpatient treatment;
  • first episode;
  • medication-naive;

Exclusion Criteria:

  • clinical diagnosis of schizophrenia, schizoaffective disorder;
  • any prescription or psychotropic medications in the past 4 week;
  • serious medical or neurological illness;
  • current pregnancy or breastfeeding.

Sites / Locations

  • ShanghaiMHCRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm 9

Arm 10

Arm 11

Arm 12

Arm 13

Arm Type

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Depression/underload 1

Depression/underload 2

Depression/underload 3

Depression/underload 4

Atypical 1

Atypical 2

Atypical 3

Atypical 4

Anxiety/somatization 1

Anxiety/somatization 2

Anxiety/somatization 3

Anxiety/somatization 4

treatment as usual(TAU)

Arm Description

This group would be treated with fluoxetine from the minimum dosage.

This group would be treated with fluoxetine combined with cognitive behavior treatment

This group would be treated with fluoxetine and amfebutamone from the minimum dosage.

This group would be treated with fluoxetine + physical treatment to help to cure depressive disorder.

This group would be treated with fluvoxamine from the minimum dosage.

This group would be treated with fluoxetine + cognitive behavior treatment

This group would be treated with fluvoxamine + lithium from the minimum dosage.

This group would be treated with fluvoxamine + lithium + physical treatment

This group would be treated with mirtazapine/selective serotonin-norepinephrine reuptake inhibitors(SNRIs) from the minimum dosage.

This group would be treated with mirtazapine/SNRIs + cognitive behavior treatment.

This group would be treated with mirtazapine + SNRIs from the minimum dosage.

This group would be treated with mirtazapine + SNRIs + physical treatment.

The investigators recommend therapy strategies according to accessible methods.

Outcomes

Primary Outcome Measures

Change from baseline in levels of microRNA,apolipoproteins, meta ion (Composite measure)
The potential biomarkers in our study include microRNA,apolipoproteins,metallic ion etc.We use quantitative analysis technique to test miRNA,proteins and metallic ion by patients' blood and urines before interventions and after interventions.

Secondary Outcome Measures

Hamilton Depression Scale(HADA) scores,reductive ratio
HADA,created by Hamilton in 1960,is one of the most common questionnaires to evaluate the severity of depression and the efficiency of medicine. we adopt the Hamilton Depression Scale(HADA)to evaluate different medicines efficiency by analyzing reductive ratio.The investigators record the total scores of HADA at baseline and 2,4,6,8,12 week.
Patient health questionnaire(PHQ-9):the clinical remission ratio
PHQ-9 is a self-report scale composed of 9 items to evaluate the state of depression.The investigators in our study record the total scores of PHQ-9 at 0,2,4,6,8,12 week to analyze the clinical remission ratio.
life event scale(LES)
LES is one of the common questionnaires to evaluate individual's mental and stress stimulation in daily life.The investigators record the total scores of LES at baseline.
social support scale(SSS)
SSS is one of the common questionnaires to evaluate individual's social support and social relationship network to explore the correlation between social support and mental health. the investigators in our study record the total scores of SSS at baseline.
dysfunctional attitudes scales(DAS)
The DAS is a self-report scale composed of 40 items to assess typical, stable depressogenic attitudes or schemas that make individuals vulnerable to depression. The investigators in our study record the total scores od DAS at baseline.
the gray matter volume,
The investigators in our study use voxel-based morphometry (VBM8)to record the gray matter volume.
fractional amplitudes of low-frequency fluctuation(fLAFF)
The investigators in our study use region-of-interest(ROI)to record fLAFF.
Neuroelectrophysiological examination: electroencephalogram(EEG)
EEG is used to record individual's brain activity. The investigators in our study record individual's brain wave.
Neuroelectrophysiological examination:electrocardiograph(ECG)
ECG is used to record the individual's cardiac cycle.

Full Information

First Posted
May 7, 2017
Last Updated
October 8, 2017
Sponsor
Shanghai Mental Health Center
Collaborators
Shanghai Jiao Tong University School of Medicine, Chinese Academy of Sciences, Shanxi Medical University, Central South University, Second Military Medical University, Peking University Sixth Hospital, First Affiliated Hospital Xi'an Jiaotong University, First Affiliated Hospital of Kunming Medical University, Air Force Military Medical University, China, Zhejiang University, Wuhan Mental Health Centre, Corning Hospital, Shenzhen City, the First Specialized Subject Hospital of Harbin, Renmin Hospital of Wuhan University, Seventh People's Hospital of Hangzhou, Shandong Mental Health Center
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1. Study Identification

Unique Protocol Identification Number
NCT03219008
Brief Title
Multi-Dimensional Diagnosis,Individualized Therapy,and Management Technique for Major Depressive Disorder:Based on Clinical and Pathological Characteristics
Acronym
STEP-MDD
Official Title
Multi-dimensional Diagnosis,Individualized Therapy,and Management Technique for Major Depressive Disorder:Based on Clinical and Pathological Characteristics
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2017 (Actual)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
December 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Mental Health Center
Collaborators
Shanghai Jiao Tong University School of Medicine, Chinese Academy of Sciences, Shanxi Medical University, Central South University, Second Military Medical University, Peking University Sixth Hospital, First Affiliated Hospital Xi'an Jiaotong University, First Affiliated Hospital of Kunming Medical University, Air Force Military Medical University, China, Zhejiang University, Wuhan Mental Health Centre, Corning Hospital, Shenzhen City, the First Specialized Subject Hospital of Harbin, Renmin Hospital of Wuhan University, Seventh People's Hospital of Hangzhou, Shandong Mental Health Center

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 is one of the most common mental diseases,which increases health-care costs and the financial burden to families and societies. Considering its complex clinical symptoms and diversity of comorbidity, depressive disorder's recognition,diagnosis,and antihistone are based on symptomatology,which is lack of multidimensional diagnosis technique based on clinical pathological characteristics,as well as lack of individualized therapy strategy based on quantified evaluation. Besides, other physical diseases,such as nervous system diseases, cardiovascular diseases,endocrine diseases, have the high comorbidity of depressive disorder. However,there is no precise diagnosis technique or standardized therapy strategy. With all those taken into consideration,our study is aimed to adopt E-mental health and m-Health to explore multi-dimensional diagnosis, individualized therapy and management technique based on molecular biology,nerve electrophysiology,and neuroimaging technology etc.
Detailed Description
Four parts included in our study: Part 1:The research, development and verification of indicators based on biomarkers and clinical characteristics to guide the diagnosis and treatment of depressive disorders to screen biomarkers, to explore its pathophysiology, and to analyze the correlation between clinical subtypes/characteristics and biomarkers. To differentiate the subtypes of depressive disorder(depression/underload, atypical, anxiety/somatization) based on clinical symptoms and clinical assessement. To establish personalized therapy strategies,and to explore tool kits for diagnosis and treatment based on biomarkers and clinical characteristics. to choose appropriate indicators to monitor therapy and side effect by collecting and analyzing blood/imaging/neuropsychological data. Part 2: The development,transition and application of hierarchical model diagnostic technique for physical diseases combined with depressive disorder. to recruit patients with physical diseases combined with depressive disorder, and explore potential biomarkers. To chose appropriate therapy strategies based on measurement based care(MBC), providing hierarchical model diagnostic technique for patients. To weigh therapy efficiency and adverse effect among different medicine therapy groups. Part3: The development and application of comprehensive prevention, diagnosis,and intervention model of depressive disorder. To explore and establish online screening and assistant diagnosis system for patients with depressive disorder. research ,development and application of intelligent e-MBC. Part 4: The development,transition and application of e-MBC sharing platform.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depressive Disorder
Keywords
depressive disorder, multi-dimensional diagnosis technique, individualized therapy, management technique, e-MBC, MBC

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Part 2: all patients before receiving any medicine treatment are divided into four groups which adopt different therapy strategies :treatment with fluvoxamine, fluoxetine, mirtazapine and treatment as usual(TAU).Meanwhile,patients with different subtypes of depressive disorder were randomly assigned to different therapy groups.Each therapy groups contains 50 participants.Therefore, the total sample size is 50*12+200=800. Part3:To find out efficiency of different kinds of therapy strategies.p=60%, error=5%,a-0.05,the amount of samples nearly is:867,considering the nearly 30% expulsion rate, the final total sample size is 867+260=1127.Therefore,sample size in each group is nearly 376. Part4:p=60%,error=0.05, a=0.05, exculsion rate=30%,N=867+260=1127.the amount of samples of each group is 1127/3=nearly 400.
Masking
ParticipantOutcomes Assessor
Masking Description
patients with depressive disorder were randomly assigned to different therapy groups or TAU therapy group based on different depressive disorders subtypes.
Allocation
Randomized
Enrollment
800 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Depression/underload 1
Arm Type
Experimental
Arm Description
This group would be treated with fluoxetine from the minimum dosage.
Arm Title
Depression/underload 2
Arm Type
Experimental
Arm Description
This group would be treated with fluoxetine combined with cognitive behavior treatment
Arm Title
Depression/underload 3
Arm Type
Experimental
Arm Description
This group would be treated with fluoxetine and amfebutamone from the minimum dosage.
Arm Title
Depression/underload 4
Arm Type
Experimental
Arm Description
This group would be treated with fluoxetine + physical treatment to help to cure depressive disorder.
Arm Title
Atypical 1
Arm Type
Experimental
Arm Description
This group would be treated with fluvoxamine from the minimum dosage.
Arm Title
Atypical 2
Arm Type
Experimental
Arm Description
This group would be treated with fluoxetine + cognitive behavior treatment
Arm Title
Atypical 3
Arm Type
Experimental
Arm Description
This group would be treated with fluvoxamine + lithium from the minimum dosage.
Arm Title
Atypical 4
Arm Type
Experimental
Arm Description
This group would be treated with fluvoxamine + lithium + physical treatment
Arm Title
Anxiety/somatization 1
Arm Type
Experimental
Arm Description
This group would be treated with mirtazapine/selective serotonin-norepinephrine reuptake inhibitors(SNRIs) from the minimum dosage.
Arm Title
Anxiety/somatization 2
Arm Type
Experimental
Arm Description
This group would be treated with mirtazapine/SNRIs + cognitive behavior treatment.
Arm Title
Anxiety/somatization 3
Arm Type
Experimental
Arm Description
This group would be treated with mirtazapine + SNRIs from the minimum dosage.
Arm Title
Anxiety/somatization 4
Arm Type
Experimental
Arm Description
This group would be treated with mirtazapine + SNRIs + physical treatment.
Arm Title
treatment as usual(TAU)
Arm Type
Experimental
Arm Description
The investigators recommend therapy strategies according to accessible methods.
Intervention Type
Drug
Intervention Name(s)
Fluoxetine
Intervention Description
Fluoxetine is one kind of selective serotonin reuptake inhibitor(SSRIs), whose effect is much better than other non-underload subtypes compared with underload subtypes.So patients would be treated with fluoxetine only.
Intervention Type
Combination Product
Intervention Name(s)
fluoxetine + cognitive-behavioral treatment(CBT)
Intervention Description
the investigators would recommend fluoxetine to help to cure depressive disorder.And CBT is a very effective way for patients to alleviate or relieve clinical symptoms during episode stage.
Intervention Type
Drug
Intervention Name(s)
fluoxetine + Amfebutamone
Intervention Description
Amfebutamone is one kind of SNRIs, and it shows much better therapy effect on patients with exhaustion /dizziness.So the investigators recommend these two drugs to help to cure patients with depressive disorder.
Intervention Type
Combination Product
Intervention Name(s)
physical treatment+fluoxetine+amfebutamone
Intervention Description
the investigators recommend drug(fluoxetine and amfebutamone) and physical treatment as intervention.
Intervention Type
Drug
Intervention Name(s)
Fluvoxamine
Intervention Description
Fluvoxamine could inhibit CYP1A2 and CYP2C19 and affect the metabolism of melatonin, and help to release symptoms of depressive disorder with sleep problems.
Intervention Type
Drug
Intervention Name(s)
Lithium+fluvoxamine
Intervention Description
the investigators recommend lithium as a mood stabilizer and use fluvoxamine to affect the level of melatonin.
Intervention Type
Combination Product
Intervention Name(s)
fluvoxamine + lithium + physical therapy
Intervention Description
the investigators recommend depressants and mood stabilizers as well as physical therapy to help to cure depressive disorder.
Intervention Type
Combination Product
Intervention Name(s)
Cognitive behavior treatment +fluvoxamine
Intervention Description
the investigators recommend behavioral therapy as well as drugs.
Intervention Type
Drug
Intervention Name(s)
Mirtazapine/SNRIs
Intervention Description
Mirtazapine is one kind of antagonist of a2 adrenergic receptors and could block 5-hydroxytryptamine2 and 5-hydroxytryptamine3,help to release symptoms like anxiety or somatization.Besides, SNRIs could also make similar effect on patients.Therefore, the investigators recommend mirtazapine/SNRIs to treat patients with depressive disorder.
Intervention Type
Combination Product
Intervention Name(s)
mirtazapine+ Cognitive behavior treatment
Intervention Description
the investigators recommend CBT and mirtazapine as interventions.The dosage and frequency would depend on patients' severity of symptoms .
Intervention Type
Drug
Intervention Name(s)
mirtazapine + SNRIs
Intervention Description
the investigator recommend mirtazapine and SNRIs to treat patients with major depressive disorder.
Intervention Type
Combination Product
Intervention Name(s)
mirtazapine + SNRIs + physical therapy
Intervention Description
the investigators would manage to use drugs and physical treatment to help to release the symptoms of depressive disorder.
Intervention Type
Other
Intervention Name(s)
TAU(treat as usual)
Intervention Description
patients in this group would receive therapy strategies according to their symptoms and preference.
Primary Outcome Measure Information:
Title
Change from baseline in levels of microRNA,apolipoproteins, meta ion (Composite measure)
Description
The potential biomarkers in our study include microRNA,apolipoproteins,metallic ion etc.We use quantitative analysis technique to test miRNA,proteins and metallic ion by patients' blood and urines before interventions and after interventions.
Time Frame
at 2,4,6,8,12 week.
Secondary Outcome Measure Information:
Title
Hamilton Depression Scale(HADA) scores,reductive ratio
Description
HADA,created by Hamilton in 1960,is one of the most common questionnaires to evaluate the severity of depression and the efficiency of medicine. we adopt the Hamilton Depression Scale(HADA)to evaluate different medicines efficiency by analyzing reductive ratio.The investigators record the total scores of HADA at baseline and 2,4,6,8,12 week.
Time Frame
at 0,2,4,6,8,12 week.
Title
Patient health questionnaire(PHQ-9):the clinical remission ratio
Description
PHQ-9 is a self-report scale composed of 9 items to evaluate the state of depression.The investigators in our study record the total scores of PHQ-9 at 0,2,4,6,8,12 week to analyze the clinical remission ratio.
Time Frame
change from baseline PHQ-9 total scores at 2,4,6,8,12 week
Title
life event scale(LES)
Description
LES is one of the common questionnaires to evaluate individual's mental and stress stimulation in daily life.The investigators record the total scores of LES at baseline.
Time Frame
at baseline
Title
social support scale(SSS)
Description
SSS is one of the common questionnaires to evaluate individual's social support and social relationship network to explore the correlation between social support and mental health. the investigators in our study record the total scores of SSS at baseline.
Time Frame
at baseline
Title
dysfunctional attitudes scales(DAS)
Description
The DAS is a self-report scale composed of 40 items to assess typical, stable depressogenic attitudes or schemas that make individuals vulnerable to depression. The investigators in our study record the total scores od DAS at baseline.
Time Frame
at baseline
Title
the gray matter volume,
Description
The investigators in our study use voxel-based morphometry (VBM8)to record the gray matter volume.
Time Frame
change from baseline neuroimaging data at 2,4,6,8,12 week
Title
fractional amplitudes of low-frequency fluctuation(fLAFF)
Description
The investigators in our study use region-of-interest(ROI)to record fLAFF.
Time Frame
change from baseline neuroimaging data at 2,4,6,8,12 week
Title
Neuroelectrophysiological examination: electroencephalogram(EEG)
Description
EEG is used to record individual's brain activity. The investigators in our study record individual's brain wave.
Time Frame
at baseline
Title
Neuroelectrophysiological examination:electrocardiograph(ECG)
Description
ECG is used to record the individual's cardiac cycle.
Time Frame
at baseline.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: aged 18-65 years; clinical diagnosis of major depressive disorder; 17-Hamilton Depression Scale>20; 14-Hamilton Anxiety Scale score<7; outpatient treatment; first episode; medication-naive; Exclusion Criteria: clinical diagnosis of schizophrenia, schizoaffective disorder; any prescription or psychotropic medications in the past 4 week; serious medical or neurological illness; current pregnancy or breastfeeding.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaohua Liu
Phone
+8613918061085
Email
liuxh_2005@126.com
Facility Information:
Facility Name
ShanghaiMHC
City
Shanghai
Country
China
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
To share raw data via the network platform named Clinical Trial Management Public Platform within 1year after the trial finished. And the platform website address is http://www.medresman.org
Citations:
PubMed Identifier
36189181
Citation
Liu H, Wu X, Wang Y, Liu X, Peng D, Wu Y, Chen J, Su Y, Xu J, Ma X, Li Y, Shi J, Yang X, Rong H, Forti MD, Fang Y. TNF-alpha, IL-6 and hsCRP in patients with melancholic, atypical and anxious depression: an antibody array analysis related to somatic symptoms. Gen Psychiatr. 2022 Sep 8;35(4):e100844. doi: 10.1136/gpsych-2022-100844. eCollection 2022.
Results Reference
derived
PubMed Identifier
35018097
Citation
Wang Y, Liu X, Peng D, Wu Y, Su Y, Xu J, Ma X, Li Y, Shi J, Cheng X, Rong H, Fang Y. A Preliminary Study of Different Treatment Strategies for Anxious Depression. Neuropsychiatr Dis Treat. 2022 Jan 4;18:11-18. doi: 10.2147/NDT.S320091. eCollection 2022.
Results Reference
derived
PubMed Identifier
33116533
Citation
Liu X, Wang Y, Peng D, Zhang H, Zheng Y, Wu Y, Su YA, Liu M, Ma X, Li Y, Shi J, Cheng X, Rong H, Fang Y. The Developmental and Translational Study on Biomarkers and Clinical Characteristics-based Diagnostic and Therapeutic Identification of Major Depressive Disorder: Study Protocol for a Multicenter Randomized Controlled Trial in China. Neuropsychiatr Dis Treat. 2020 Oct 9;16:2343-2351. doi: 10.2147/NDT.S271842. eCollection 2020.
Results Reference
derived

Learn more about this trial

Multi-Dimensional Diagnosis,Individualized Therapy,and Management Technique for Major Depressive Disorder:Based on Clinical and Pathological Characteristics

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