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Depressive Disorder clinical trials

View clinical trials related to Depressive Disorder.

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NCT ID: NCT02185482 Completed - Depression Clinical Trials

Physician Led Counseling in Management of Depression in Type 2 Diabetes Mellitus

Start date: August 2014
Phase: N/A
Study type: Interventional

There is a high prevalence of depression in patients with diabetes mellitus. Depression has been shown to be associated with poor self-management (adherence to diet, exercise, checking blood glucose levels) levels in patients with diabetes.To determine whether enhancing quality physician's care for depression improves both depression and diabetes outcomes in patients with depression and diabetes.

NCT ID: NCT02184481 Completed - Depression Clinical Trials

Working Memory Training for Dysphoric Students

Start date: September 2013
Phase: N/A
Study type: Interventional

Depression is associated with impairments in executive functions, including working memory (WM) which is needed to maintain and manipulate goal-relevant information. Due to these WM impairments depressed individuals have difficulties inhibiting and shifting from irrelevant (negative) information and updating goal relevant information. This study explored whether training WM decreases these impairments and reduces clinical symptoms of depression, anxiety and rumination. Sixty-one students with an elevated score on the BDI-II, representing a dysphoric mood state, executed a working memory training (n = 34) or placebo training (n = 27). Before and after training their depression, anxiety, rumination and working memory were assessed. Furthermore, they executed a working memory task while their pupil dilation was measured to assess their fatigue. Moreover, the investigators compared the dysphoric students with a healthy student population on all measures.

NCT ID: NCT02184221 Completed - Clinical trials for Major Depressive Disorder

Deep-brain Magnetic Stimulation (DMS) in the Treatment of Major Depressive Disorder

DTMS
Start date: May 2010
Phase: N/A
Study type: Interventional

Transcranial magnetic stimulation (TMS) is an effective alternative for pharmacotherapy in major depressive disorder, but the effectiveness is not clear due to stimulated region, frequency and intensity of magnet field. Standard TMS techniques only can stimulate superficial cortical areas as the electric field decreases rapidly as a function of tissue depth,while depression is also interconnected with deeper neuronal regions. Deep-brain magnetic stimulation (DSM, or deep TMS, DTMS) allows stimulation of deeper cortical regions. Previous research has demonstrated that alpha frequency (8-13 Hz) EEG activity may have particular relevance to the response to antidepressants, and reduction of alpha frequency (8-13 Hz) could lead to negative symptoms. It has been reported that both alpha frequency and low-field magnetic stimulation could improve depressive symptoms. The objective of this study is to compare the effectiveness of the two different parameters of DMS in the treatment of major depressive disorder. The changes of brain derived neurotropic factor (BDNF) are also investigated to make a relevant analysis of the improvement of depressive symptoms.

NCT ID: NCT02181231 Completed - Depression Clinical Trials

Buprenorphine Used With Treatment Resistant Depression in Older Adults

IRLGreyB
Start date: June 1, 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The investigators are conducting a research study to learn about the safety and benefit of using a medication called buprenorphine for patients with difficult to treat depression. This research study is testing whether combining two medications will be effective in treating depression when initial treatment with just one antidepressant does not relieve the depressive symptoms; this is what is called "difficult to treat depression" or "treatment resistant depression". The two medications the investigators are using are: an anti-depressant medication called venlafaxine extended release (venlafaxine XR), which is the generic form of Effexor, and buprenorphine. Buprenorphine is a medication that is FDA approved for the treatment of opioid dependence. The investigators are testing whether adding buprenorphine to venlafaxine XR enhances treatment response.

NCT ID: NCT02180607 Completed - Clinical trials for Major Depressive Disorder

Neuronal Responses to Social Feedback in Major Depressive Disorder

Start date: October 2013
Phase: N/A
Study type: Observational

The overall goal of the proposed project is to investigate the neuronal pathways regulating the effects of social acceptance and rejection in healthy controls and patients with Major Depressive Disorder (MDD). Social acceptance and rejection are defined as the explicit declaration that an individual is liked or not liked. Social acceptance can boost one's self-esteem and mood, whereas rejection can lower them. The neurological relationship between social acceptance/rejection and depressive symptoms is not known. Using functional magnetic resonance imaging (fMRI), it is hypothesized that social feedback will activate a specific interconnected neuronal pathway involved in social separation and reward. Executive functioning and response to monetary reward will also be assessed during fMRI using two additional tasks (monetary incentive delay, parametric go no-go) to determine how these cognitive brain functions regulate responses to social feedback.

NCT ID: NCT02176421 Completed - Clinical trials for Infra-orbital Skin Depressions

A Prospective, Open Label Study Evaluating JUVÉDERM® VOLBELLA With Lidocaine Treatment for the Correction of Skin Depressions in the Infra-orbital Area

Start date: May 15, 2014
Phase: N/A
Study type: Interventional

A prospective, open label, study evaluating JUVÉDERM® VOLBELLA with lidocaine treatment for the correction of skin depressions in the infra-orbital area (under the eyes)

NCT ID: NCT02176408 Completed - Clinical trials for Major Depressive Disorder

Efficacy of Adjunctive Exercise for the Behavioral Treatment of Major Depression

Start date: June 2014
Phase: N/A
Study type: Interventional

Major depressive disorder (MDD) is the leading cause of disability in the developed world and is associated with lost productivity, increased health care utilization, and mortality. Several empirically supported treatments, such as antidepressant medication and cognitive behavioral therapy, exist for the treatment of MDD; however, studies have shown that as many as 34% of individuals do not respond to these treatments. Exercise and stretching interventions represent alternative strategies associated with strong effect sizes in past studies. Additionally, exercise has been shown to enhance cognitive functioning, especially attention and memory. This study aims to investigate the effect of a combined aerobic exercise and behavioral activation treatment (BA) for MDD. Behavioral activation treatment involves completing both pleasant and mastery-based activities with the goal of enhancing mood. The current study will recruit 32 MDD patients for an active treatment phase of nine 60-90 minute sessions (6 weekly sessions and 3 biweekly sessions) of either BA plus exercise (BA+EX) or BA plus stretching (BA+STR). The purpose of this study is to identify if adding aerobic exercise to a brief psychosocial treatment can improve mood above and beyond an active control condition.

NCT ID: NCT02176291 Completed - Depression Clinical Trials

Incomplete Response in Late-Life Depression: Getting to Remission With Buprenorphine

IRLGREY-B
Start date: August 2014
Phase: Phase 2
Study type: Interventional

The purposes of this project are to examine the feasibility, safety, tolerability and clinical effect of low-dose buprenorphine as a novel treatment for late-life treatment-resistant depression and to develop preliminary data about mechanism of action.

NCT ID: NCT02176226 Completed - Clinical trials for Major Depressive Disorder

IntelliCare: Artificial Intelligence in a Mobile Intervention for Depression and Anxiety (AIM)

Start date: March 2015
Phase: N/A
Study type: Interventional

This study will evaluate a Smartphone intervention for depression and anxiety that uses machine learning to tailor treatment for patients. The intervention, referred to as IntelliCare, delivers patient-specific treatment material and motivational messaging via a mobile phone, to help individuals with depression and/or anxiety. Information and data received from the patient will inform the tailored treatment approach through machine learning. The purpose of this study is to obtain preliminary information on the feasibility and effectiveness of IntelliCare in improving symptoms of depression and anxiety.

NCT ID: NCT02171923 Completed - Major Depression Clinical Trials

Multicenter Comparative Study of the Activity of the Medial Prefrontal Cortex in Vulnerability to Depression

CORVAD
Start date: May 2013
Phase: N/A
Study type: Observational

To examine whether the medial prefrontal cortex displays an increased activity during self-referential processing among remitted depressed patients compared to healthy controls