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Depressive Disorder clinical trials

View clinical trials related to Depressive Disorder.

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NCT ID: NCT00513565 Completed - Clinical trials for Depressive Disorder and Anxiety Disorders

A Study To Investigate Effects Of GSK561679 On Brain Activation During Emotional Processing In Healthy Volunteers

Start date: September 13, 2007
Phase: Phase 1
Study type: Interventional

This study will be conducted in healthy volunteers to investigate the effect of single dose GSK561679 on the changes of brain activation, as it compares to an active comparator, lorazepam.

NCT ID: NCT00511810 Completed - Clinical trials for Major Depressive Disorder

Omega-3 Fatty Acids as Adjunct Treatment for Major Depressive Disorder

Start date: August 2007
Phase: Phase 2/Phase 3
Study type: Interventional

The primary objective of the study was to determine the effects of 10-week adjunctive supplementation with 2 doses of LCn-3 fatty acids (fish oil) on cortical functional activity and biochemistry in adolescents with MDD. The primary prediction was that LCn-3 fatty acid supplementation would dose-dependently increase prefrontal cortical functional activation during sustained attention and increase regional biochemical indices of cortical metabolism and integrity concentrations in association with reductions in depressive symptoms.

NCT ID: NCT00511680 Completed - Depression Clinical Trials

Beat the Blues: Treating Depression in African American Elders

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The specific primary aims of the study are to: 1. Test the immediate effect of the intervention at 4-months on depression in urban African American older adults (primary trial outcome; between group comparison). Hypothesis: Participants in the intervention group will report fewer depressive symptoms in comparison to control group participants receiving usual care. 2. Test the maintenance effect of the intervention at 8-months on depression (within group comparison). Hypothesis: Participants in the intervention group will maintain reduced symptom presentation from 4 to 8 months. 3. Evaluate acceptability (social validity) of the intervention and extent of engagement in activities by study participants (both intervention and wait-list control subjects). A secondary aim of this study is to assess the feasibility of conducting a clinical trial embedded in a community service setting and its dissemination using a community-academic partnership. We also propose three exploratory aims. First, we seek to evaluate the mechanisms of action, or pathways, by which treatment gains are obtained (Gitlin et al., 2000). Given that behavioral activation represents conceptually the key active ingredient of the proposed intervention, we plan to evaluate its mediational effect. Second, we seek to evaluate whether the intervention has a differential treatment effect based on a study participant's gender, age, and living arrangement (alone or with others). Given that previous research suggests that participant characteristics may moderate depressive symptoms and treatment outcomes, these exploratory analyses will provide insight as to whether this particular treatment benefits some groups more than others. Third, we seek to evaluate whether the intervention has short and long-term effects on quality of life, functional difficulty, and self-efficacy to manage day-to-day tasks. Previous research has shown that depressive symptoms exacerbate functional decline such that minimizing distress may have the added value of enhancing function and perceived efficacy for this group over time.

NCT ID: NCT00511654 Completed - Depressive Disorder Clinical Trials

28-day Repeat Dose and Drug Interaction Study With Orvepitant (GW823296)

Start date: June 12, 2007
Phase: Phase 1
Study type: Interventional

This study is being conducted to obtain information on the safety and tolerability of repeated doses of GW823296 for 28 days in healthy male and female subjects. In addition, the pharmacokinetics of GW823296 will be evaluated to confirm the doses to be used in Phase II efficacy studies. The effect of repeat dose (RD) of GW823296 on CYP3A4 enzyme activity will be investigated evaluating the pharmacokinetics of midazolam and urine 6-?-hydroxycortisol/cortisol ratio.

NCT ID: NCT00510822 Completed - Major Depression Clinical Trials

Cimicoxib for the Treatment of Major Depression (SECIM)

Start date: October 2007
Phase: Phase 2
Study type: Interventional

This multicenter study aims to investigate the safety and efficacy of cimicoxib, a selective COX-2 inhibitor, in combination with sertraline compared to sertraline combined with placebo in patients with major depression. This clinical study is based on the assumption that adjunctive treatment of major depression with a COX-2 inhibitor may be beneficial.

NCT ID: NCT00508859 Completed - Depression Clinical Trials

Maintenance Study for Adolescent Depression

MTAD
Start date: July 1997
Phase: Phase 4
Study type: Interventional

This study examined the benefit of continued treatment with an antidepressant medication, sertraline, in adolescents with depression who improved on sertraline acutely. We hypothesize that adolescents who remained on sertraline long term were less likely to have a recurrence of depression compared to those on placebo.

NCT ID: NCT00505518 Completed - Clinical trials for Major Depressive Disorder

Investigating the Effectiveness of Telepsychiatry for Treating Major Depression in a Chinese American Nursing Home

Start date: September 2006
Phase: N/A
Study type: Interventional

The current use of telepsychiatry, or psychiatric care using videoconferencing, is very limited. The present study investigates the use of this method with a depressed Chinese American population in a nursing home. It is believed that this population can benefit from telepsychiatric treatment when used in collaboration with the primary care they receive in the nursing home.

NCT ID: NCT00498706 Completed - Depression Clinical Trials

Effectiveness of Telephone Versus Face-to-Face CBT in Treating People With Depression

Start date: December 2007
Phase: Phase 3
Study type: Interventional

This study will compare the effectiveness of telephone versus face-to-face administration of cognitive behavioral therapy in treating people with depression.

NCT ID: NCT00497874 Completed - Depression Clinical Trials

An Expert System to Reduce Depression in Primary Care

Start date: July 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether a home-based intervention matched to stage of change (readiness) for using effective methods to prevent or reduce depression can improve depression outcomes in primary care.

NCT ID: NCT00494377 Completed - Depression Clinical Trials

Duloxetine Versus Duloxetine Plus Non-Drug Therapy for Depression

Start date: February 2004
Phase: Phase 4
Study type: Interventional

The primary purpose of this study is to determine if duloxetine plus non-drug intervention is more effective than duloxetine alone in patients with depression.