Skip to main content
Clinical Trials/NCT05529576
NCT05529576
Unknown
Phase 4

Multi-factor Model Constraction for Early Warning and Diagnosis of Major Depressive Disorder

Shanghai Mental Health Center1 site in 1 country600 target enrollmentAugust 23, 2022

Overview

Phase
Phase 4
Intervention
Omega 3 fatty acid
Conditions
Major Depressive Disorder
Sponsor
Shanghai Mental Health Center
Enrollment
600
Locations
1
Primary Endpoint
Depressive symptoms assessed by HAMD-17
Last Updated
3 years ago

Overview

Brief Summary

Current research on the pathogenesis of depression shows that imbalanced inflammatory factors are closely related to Major Depressive Disorder(MDD). As reported, physical exercise, Ω-3 fatty acids, and sulforaphane can be complementary therapies for moderate-to-severe depression. In addition, imaging studies have found changes in the structure and functional connectivity of the brain. Therefore, this study intends to collect clinical and biological information from patients with depression and healthy controls to establish a multi-factor model for early warning and diagnosis of major depressive disorder

Detailed Description

The immune imbalance has been reported in patients with unipolar and bipolar depression. There is no unified conclusion in the field and severity of the immune imbalance, and the cause of cognitive impairment is unknown, which may be related to many factors. Omega-3 fatty acids are immune modulators that possess antidepressant effects. This study includes three steps. 1. We will enroll bipolar and major depressive disorder patients who are in a depressive episode and enroll healthy controls. All subjects will be assessed at baseline 2. We will give omega-fatty acid treatment based on immune indicators 3. The follow-up will last for one year with five sessions.

Registry
clinicaltrials.gov
Start Date
August 23, 2022
End Date
December 31, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Outpatients in main-center and sub-centers
  • Age between 18-65 years old
  • Meet the DSM-IV diagnosis of depressive episode
  • HAMD-17 score\>17 at baseline
  • No antidepressant treatment within 6 weeks prior to enrollment
  • Adequate cognition level to complete the tests necessary for the study
  • Willing to sign the informed consent form

Exclusion Criteria

  • Have any contraindications to Ω-3 fatty acids
  • Severe physical disease
  • Diagnosed with schizophrenia, or other mental illness spectra
  • Have received physical therapy

Arms & Interventions

Major depressive disorder

Outpatients in main-center and sub-centers; meet the DSM-IV diagnosis of Major Depressive Disorder (mental examination was conducted by at least two professional doctors); available relevant HIS system biochemical data; haven't been treated with physical therapy; age between 18-65 years old; gender is not limited.

Intervention: Omega 3 fatty acid

Bipolar disorder

Outpatients in main-center and sub-centers; meet the DSM-IV diagnosis of Bipolar disorder (mental examination was conducted by at least two professional doctors); available relevant HIS system biochemical data; haven't been treated with physical therapy; age between 18-65 years old; gender is not limited

Intervention: Omega 3 fatty acid

Outcomes

Primary Outcomes

Depressive symptoms assessed by HAMD-17

Time Frame: up to 12 months

Depressive symptoms are the primary outcome, and we will use HAMD-17 to examine depressive symptoms. Respones: a reduction of 50% or more in baseline scores.Remission:HAMD⩽7.

Study Sites (1)

Loading locations...

Similar Trials