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Depressive Disorder, Major clinical trials

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NCT ID: NCT02800226 Completed - Clinical trials for Major Depressive Disorder

Pilot Study Comparing 10hz vs Theta Burst Stimulation

Start date: March 2014
Phase: Phase 3
Study type: Interventional

This pilot study aims at exploring the efficacy of iTBS compared to 10Hz protocol and explore potential biomarkers of treatment response

NCT ID: NCT02793258 Completed - Clinical trials for Major Depressive Disorder

Impact of tDCS on Emotional Processing in Major Depression

EmoStim
Start date: July 22, 2016
Phase: N/A
Study type: Interventional

Background: transcranial direct current stimulation (tDCS) is an innovative treatment for major depression. However, its mechanisms of action are still unclear. Major depression is characterized by impaired processing of emotional information, which returns back to normal after successful antidepressant treatment. In this randomized double-blind study, the investigators aim to assess the effect of tDCS on emotional processing in major depression.

NCT ID: NCT02777112 Completed - Depression Clinical Trials

The Effects of E-mental Health Program and Job Coaching on the Risk of Major Depression in Canadian Working Men

Start date: September 2016
Phase: N/A
Study type: Interventional

There is a pressing need for innovation in prevention of major depression in male workers. Major depression (MDE) affects workers' health and productivity. In the United States, workers with depression cost an estimated US $44.01 billion per year in lost productivity. One of the severe consequences of having MDE is potential suicide and Canadian national data showed that 76% of all suicides in 2009 were male. In the workplace, risk factors for having MDE differ for men and women. For instance, job strain, family to work conflict and job insecurity seem to be more prominent MDE risk factors in men than in women. Compounding men's risk, men are less likely than women to seek help and to disclose depressive symptoms and often delay help seeking until symptoms become severe. Men are socialized to be emotionally stoic and exemplify traditional masculine characteristics such as independence, self-reliance and dominance. Men are concerned over the perceived negative judgments from family and friends if they access treatment for depression. These gender specific experiences along with a limited knowledge base about effective interventions call for innovative solutions tailored for men. The proposed study was to evaluate the effectiveness of an e-mental health program on reducing the risk of major depression in Canadian working men.

NCT ID: NCT02773108 Completed - Schizophrenia Clinical Trials

Somatic Comorbidities in Psychiatric Patients

SCPP
Start date: May 2016
Phase:
Study type: Observational

Prevalence of somatic comorbidities in psychiatric patients hospitalized in Psychiatric hospital or treated ambulatory or in daily hospital. Comparison of prevalence of somatic comorbidities in psychiatric patients population and the general Croatian population.

NCT ID: NCT02752724 Completed - Clinical trials for Major Depressive Disorder

Ketamine Anesthesia for Improvement of Depression in ECT

KAID
Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of this prospective randomized clinical trial is to determine if patients receiving ketamine as a part of general anesthesia during electroconvulsive therapy (ECT) rather than standard of care will have improvement in symptoms of depression after a course of ECT treatments. The investigators hypothesize that utilization of ketamine for induction of general anesthesia during ECT treatments will improve symptoms of depression better than standard care. This study is ONLY open to patients eligible to receive healthcare services through the Department of Veterans Affairs at the VA Puget Sound, which means service in the active military, naval or air service or separation under any condition other than dishonorable. Qualifications for VA health care benefits can be found at va.gov.

NCT ID: NCT02752178 Completed - Clinical trials for Depressive Disorder, Major

Peripheral Immunomarker Validation in Treatment-resistant Depression

BIODEP
Start date: June 2015
Phase:
Study type: Observational

This is a study to characterise the role of inflammatory processes in depression. There is compelling evidence that inflammation is often associated with, and can cause, depression. It is currently less clear that antiinflammatory drugs have meaningful antidepressant effect. One of the goals is to identify the subset of depressed patients that is most likely to respond better to an antiinflammatory drug than to a conventional antidepressant. The investigators will therefore undertake a study of patients with a diagnosis of major depressive disorder including four groups: i) incompletely responsive patients who have demonstrated failure to respond consistently or completely to standard treatment, ii) those who have responded well to treatment and are not currently depressed, iii) untreated patients who are currently depressed, iv) healthy volunteers with no history of depression. Participants will undergo a clinical assessment, an interview with a trained member of the research team and will complete self-rated questionnaires. Investigators will collect blood and saliva samples to measure certain immune markers. They will also perform magnetic resonance imaging (MRI) scans to look for MRI markers in the brain and investigate brain inflammation in a subsample of these patients using positron emission topography (PET) and cerebrospinal fluid (CSF) sampling (also called lumbar puncture).

NCT ID: NCT02749721 Completed - Clinical trials for Major Depressive Disorder

The Relationship Among Changes in Brain Network Activation in Adult Outpatients With Major Depressive Disorder

Start date: December 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to explore patterns of Brain Network Activation (BNA) changes from baseline to endpoint on 1) efficacy of core symptoms of Major Depressive Disorder (MDD) and 2) improvement of cognitive dysfunction with acute treatment with flexible dose vortioxetine in adult outpatients with MDD and subjective complaints of cognitive dysfunction.

NCT ID: NCT02747134 Completed - Clinical trials for Major Depressive Disorder

Combining Emotion Regulation and Mindfulness Skills for Preventing Depression Relapse

Start date: September 2008
Phase: N/A
Study type: Interventional

In the present study researchers aim to investigate the effectiveness of an intervention combining emotion regulation and mindfulness skills in a single 10-week program. A total of 75 individuals with major depressive disorder (MDD) diagnosis in complete or partial remission participated in this randomized controlled trial (RCT) comparing an intervention including emotion regulation and mindfulness skills (ER+M) with a psychoeducative program. After treatment, participants were followed for a 1-year period. Researchers results indicate that ER+M was not more effective than the treatment used with the control group in preventing depression relapse. Participants allocated to the ER+M group showed a significant decrease on global psychiatric symptoms, whereas those in the control group did not. Further studies are needed in order to better determine the combined effects of mindfulness and behavioral activation.

NCT ID: NCT02746367 Completed - Clinical trials for Major Depressive Disorder, Bipolar I and Bipolar II

Bipolar Proteomic Assay Validation Study

Start date: March 2016
Phase:
Study type: Observational

The purpose of this study is to validate a set of signatures, based on a panel of proteomic markers, that discriminate BDI, BDII, and MDD in people seeking treatment for a depressive episode.

NCT ID: NCT02744391 Completed - Clinical trials for Major Depressive Disorder

A Study of L-DOPA for Depression and Slowing in Older Adults

Start date: August 24, 2016
Phase: Phase 4
Study type: Interventional

Individuals with Late Life Depression (LLD) often have cognitive problems, particularly problems with memory, attention, and problem solving, all of which contribute to antidepressant non-response. Our group and others have shown that decreased thinking speed is the central cause of functional problems in patients with LLD. Similarly, decreased walking speed is associated with depression and carries additional risk for falls, hospitalization, and death. Available evidence suggests that declining functionality in the brain's dopamine system contributes to age-related cognitive and motor slowing. The central hypothesis of this R61/R33 Phased Innovation Award is that by enhancing dopamine functioning in the brain and improving cognitive and motor slowing, administration of carbidopa/levodopa (L-DOPA) will improve depressive symptoms in older adults.