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Clinical Trials/NCT04528628
NCT04528628
Unknown
Not Applicable

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

Shanghai Mental Health Center4 sites in 1 country960 target enrollmentOctober 2020

Overview

Phase
Not Applicable
Intervention
SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors)
Conditions
Major Depressive Disorder
Sponsor
Shanghai Mental Health Center
Enrollment
960
Locations
4
Primary Endpoint
remission of acute phase
Last Updated
5 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 2020
End Date
September 2022
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

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.

Arms & Interventions

MDD with melancholic features

Intervention: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors)

MDD with melancholic features

Intervention: Treatment as Usual

MDD with melancholic features

Intervention: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) Combined with Magnetic Stimulations

MDD with atypical features

Intervention: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors)

MDD with atypical features

Intervention: Treatment as Usual

MDD with atypical features

Intervention: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) Combined with Magnetic Stimulations

MDD with anxious distress

Intervention: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors)

MDD with anxious distress

Intervention: Treatment as Usual

MDD with anxious distress

Intervention: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) Combined with Magnetic Stimulations

MDD (overall)

Intervention: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors)

MDD (overall)

Intervention: Treatment as Usual

MDD (overall)

Intervention: SSRIs/SNRIs (Selective Serotonin Reuptake Inhibitors/ Serotonin and Norepinephrine Reuptake Inhibitors) Combined with Magnetic Stimulations

Outcomes

Primary Outcomes

remission of acute phase

Time Frame: 12 weeks

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

Study Sites (4)

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