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Major Depressive Disorder clinical trials

View clinical trials related to Major Depressive Disorder.

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NCT ID: NCT02959307 Completed - Depression Clinical Trials

Transcranial Laser Therapy, Continuous and Pulsed Light, for Major Depressive Disorder (ELATED-3)

ELATED-3
Start date: November 2016
Phase: N/A
Study type: Interventional

Transcranial Light Therapy involves non-invasive and invisible beams of light that increase energy metabolism in the brain. Transcranial light therapy has been found to promote brain metabolism which may help people with depression. The research team proposes a novel approach to treating depression by using transcranial light therapy.

NCT ID: NCT02948036 Completed - Clinical trials for Major Depressive Disorder

A Closed-loop Assessment and Treatment Platform for Unipolar Depression and Anxiety

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

Specific Aim 1: Finalize development of the closed-loop strategy in the MMT application. Specific Aim 2: Evaluate the acceptability and feasibility of the MMT application with the target population to prepare for a large-scale efficacy trial.

NCT ID: NCT02939560 Completed - Depression Clinical Trials

TMS for Adults With Autism and Depression

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

The goal of this proposal is to investigate whether a standard rTMS protocol for depression, including multiple sessions applied to left dorsolateral prefrontal cortex (DLPFC) results in reduction of depressive symptoms for adult patients with ASD and MDD (Aim 1). The secondary goal is to investigate and whether there is any beneficial reduction in the core symptoms of autism (Aim 2).

NCT ID: NCT02935647 Completed - Clinical trials for Major Depressive Disorder

Burst Suppression Anesthesia for Treatment of Severe Depression

Start date: October 1, 2016
Phase: Phase 1
Study type: Interventional

This study is designed to determine if the antidepressant effects of deep anesthesia via propofol are related to EEG burst suppression.

NCT ID: NCT02934334 Completed - Clinical trials for Major Depressive Disorder

Wellness Monitoring for Major Depressive Disorder

CBN-Well
Start date: May 31, 2016
Phase:
Study type: Observational

The Wellness Monitoring for Major Depressive Disorder (MDD) study is a prospective, longitudinal, observational study aimed at identifying biomarkers of relapse in MDD. Results may help refine clinical approach to relapse management, and may ultimately help MDD patients sustain wellness while on antidepressant medication.

NCT ID: NCT02922556 Completed - Clinical trials for Major Depressive Disorder

Piloting a Novel, Mobile Cognitive Training Tool for Patients With Major Depressive Disorder (MDD)

MDD
Start date: September 2015
Phase: N/A
Study type: Interventional

To assess the efficacy of a mobile-device-deployed cognitive emotional treatment for depression (Moodify) versus an active control treatment (commercially available computer games).

NCT ID: NCT02907476 Completed - Depression Clinical Trials

The Treatment of Depression With Yoga and Walking

Start date: January 4, 2017
Phase: N/A
Study type: Interventional

This randomized controlled trial is designed to test the Vagal-gamma amino-butyric acid (GABA) Hypothesis that one of the mechanisms by which yoga-based practices improve mood and decrease anxiety is by correcting an autonomic system (ANS) imbalance with too much activity in the sympathetic nervous system (SNS) and too little activity in the parasympathetic nervous system (PNS). This imbalance is associated with under activity in the GABA system. It is hypothesized that yoga-based practices increase activity in the PNS by increasing respiratory sinus arrhythmia (RSA), which is associated with increased activity in the GABA system and decreased depressive and anxiety symptoms.

NCT ID: NCT02900092 Completed - Clinical trials for Major Depressive Disorder

Augmentation of Treatment-Resistant Depression With An Analog of the Neuroactive Steroid Allopregnanolone

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

Major depressive disorder (MDD) is highly prevalent and nearly 70% of individuals with MDD do not respond to standard antidepressant therapies despite adequate dosing. An effective and well-tolerated antidepressant augmentation therapy would have important clinical and public health implications. Neuroactive steroid hormones are known to directly activate neurotransmitter receptors in the brain, and thus are potential candidates for augmentation therapies to enhance the effect of traditional antidepressants. The investigators hypothesize that administration of an allopregnanolone analog in women with treatment-resistant depression will improve depressive symptoms.

NCT ID: NCT02874131 Completed - Clinical trials for Major Depressive Disorder

Behavioral Activation + Cognitive Processing Therapy for PTSD and Comorbid MDD

Start date: October 20, 2015
Phase: N/A
Study type: Interventional

This study is a randomized controlled trial comparing an integrated treatment, Behavioral Activation + Cognitive Processing Therapy (BA + CPT), to CPT alone among active-duty service members with posttraumatic stress disorder (PTSD) and comorbid major depressive disorder (MDD). Participants will complete assessor-administered and self-report measures at pre- and post-treatment assessments, as well as a 3-month follow-up. Additionally, participants will complete self-report measures of PTSD and MDD symptoms at each therapy session.

NCT ID: NCT02871141 Completed - Clinical trials for Major Depressive Disorder

Multimodal Imaging of ECT Effects

Start date: September 1, 2017
Phase:
Study type: Observational [Patient Registry]

The project aims to investigate markers of neural activity and connectivity, neurochemistry, hypothalamic-pituitary-adrenal (HPA) axis activity, inflammation and neuronal plasticity underlying treatment response and remission after ECT. These measures will be assessed in depressive patients prior, during and after ECT and also after 6 months. Furthermore, we will investigate a control group of depressive patients treated with antidepressants.