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Major Depression clinical trials

View clinical trials related to Major Depression.

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NCT ID: NCT01191580 Completed - Major Depression Clinical Trials

Interpersonal Therapy for Depression in Breast Cancer

Start date: October 2009
Phase: Phase 4
Study type: Interventional

The investigators propose a randomized clinical trial to compare the efficacy of Interpersonal Psychotherapy (IPT), Problem-Solving Therapy (PST), and Brief Supportive Psychotherapy (BSP), in improving depressive symptoms, psychosocial functioning, and quality of life among patients with breast cancer and major depressive disorder (MDD).

NCT ID: NCT01178424 Completed - Major Depression Clinical Trials

My Depression Wellness Toolkit Study

Start date: August 2010
Phase: N/A
Study type: Interventional

Major depressive disorder (MDD) continues to have a profound impact on individuals, families, and the health care system. Despite marked success in treating active individual episodes of unipolar depression, our understanding of the neural and cognitive mechanisms involved in the return of symptoms remains extremely limited, and few interventions exist that specifically target factors involved in prophylaxis. The research being proposed is among the first that is designed to examine neurocognitive markers for depressive relapse vulnerability and link them directly to clinical prognosis. Hypothesis 1: Cortical midline structures (CMS) network recruitment will be associated with behavioural and neural indices of a reflexive attentional bias towards dysphoric stimuli in a divided attention task. Hypothesis 2: Behavioural and neural indices of dysphoric attentional bias following mood challenge will predict depression relapse in prospective 18-month follow up. Hypothesis 3: Relative to CBT, Mindfulness Based Cognitive Therapy (MBCT) will normalize CMS and right insular/fronto-opercular cortices (INS-FO) network imbalance. Hypothesis 4: Relative to CBT, MBCT will normalize to healthy control levels, behavioural and neural indices of dysphoric attentional bias, which will be predictive of reduced relapse risk across a 24 month follow up.

NCT ID: NCT01178255 Terminated - Major Depression Clinical Trials

Efficacy and Safety of Homeopathy for Moderate Depression (Acute Phase)

DEP-HOM
Start date: August 2010
Phase: Phase 3
Study type: Interventional

To assess the two components of individualized homeopathic treatment for acute depression, i.e., to investigate the specific effect of individualized Q-potencies versus placebo and to investigate the effect of different approaches to the homeopathic case history taking(defined in this study as case history taking type I and II).

NCT ID: NCT01153139 Completed - Major Depression Clinical Trials

Long-term Bilateral Theta Burst Stimulation for the Treatment of Major Depression

TheBuS_D
Start date: April 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Repetitive transcranial magnetic stimulation has been shown to be moderately effective in the treatment of major depression. Theta burst stimulation (TBS) is a new form of rTMS that may exert larger effects. This sham-controlled study examines the effectivity of daily bilateral TBS to the dorsolateral frontal cortex over 6 weeks in 2x16 patients with major depression add on to the local standard of a combined pharmacological/psychotherapeutical treatment.

NCT ID: NCT01150604 Completed - Depression Clinical Trials

Depression Management Project

DMP
Start date: June 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether an eight-lesson self-help intervention delivered online will result in a reduction of depressive symptoms.

NCT ID: NCT01147913 Completed - Major Depression Clinical Trials

Computerized Information-Processing Bias Retraining in Depressed Adolescents

Start date: March 2010
Phase: Phase 2
Study type: Interventional

This study will examine how well a novel four-session computerized program, designed to help adolescents learn to interpret ambiguous situations less negatively, reduces symptoms of depression and decreases negative information-processing biases.

NCT ID: NCT01135758 Terminated - Major Depression Clinical Trials

Study of Depression-Ketamine-Brain Function

Start date: June 2010
Phase: Phase 2
Study type: Interventional

Targeting the glutamatergic system to treat depression is a new and promising strategy based on studies at the molecular, synaptic, and neuronal level but also on results of studies conducted in animal models and first clinical studies involving depressed patients.Ketamine has been proposed as a novel approach to induce rapid antidepressant response. In this pilot project the investigators aim to introduce this novel and promising approach into clinical practice. Besides the assessment of clinical efficacy, the investigators will put a special emphasis on the assessment of ketamine-associated effects on brain function using fMRI and cognitive testing.

NCT ID: NCT01132872 Completed - Depression Clinical Trials

PET Whole Body Distribution Studies Using [11C]CUMI

Start date: April 30, 2010
Phase: N/A
Study type: Observational

Background: - Researchers studying new treatments for major depressive disorder are looking at how medications to treat depression act on the brain chemical serotonin, which interacts with specific serotonin receptors on brain cells. New methods of studying serotonin receptors in the brain may help provide a better understanding of depression and treatment options. - A new radioactive chemical called [11C]CUMI may be useful for studying serotonin receptors in the brain. By using positron emission tomography (PET) scanning to see how [11C]CUMI bonds with serotonin receptors, researchers will investigate whether [11C]CUMI can be used to study depression and how antidepressant medications work. Objectives: - To determine the usefulness of [11C]CUMI as a method of studying serotonin receptors in the brain. Eligibility: - Healthy individuals between 18 and 65 who have no history of psychiatric illness. Design: - This study requires 8 outpatient visits to the NIH clinic. - Visit 1: Participants will have a full physical examination and medical history, as well as a psychiatric evaluation and questions about alcohol and drug use. Other tests will include blood and urine samples and an electrocardiogram (EKG). Testing will take approximately 3 hours. - Visit 2: Participants will have a magnetic resonance imaging (MRI) scan to evaluate brain function and activity. - Visit 3: Participants will have a PET scan, in which a small amount of the radioactive chemical [11C]CUMI will be injected through an intravenous (IV) catheter, and will have another IV line put in place to draw regular blood samples during the scan. The scan will last approximately 4 hours. - Visits 4-8: Participants will have regular blood tests after the scan between days 1-3 and at about weeks 1, 2, 3, and 4. The blood tests will check muscle, heart, and liver function.

NCT ID: NCT01124344 Terminated - Major Depression Clinical Trials

Safety and Pharmacology Study of BMS-866949

Start date: May 2010
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to determine whether multiple doses.of BMS-886949 are safe and tolerable

NCT ID: NCT01119430 Terminated - Major Depression Clinical Trials

Fluoxetine Versus Fluoxetine Plus DU125530 in Major Depressive Disorder

Start date: May 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to examine whether the speed of the clinical antidepressant action of fluoxetine can be accelerated by administering DU125530 a full 5-HT1A antagonist.