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Mood Disorders clinical trials

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NCT ID: NCT00794040 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

A Controlled Trial of Serotonin Reuptake Inhibitors Added to Stimulant Medication in Youth With Severe Mood Dysregulation

Start date: November 17, 2008
Phase: Phase 2
Study type: Interventional

Severe mood dysregulation (SMD) is a very common syndrome in children. Its symptoms include very severe irritability, including persistent anger and frequent outbursts, as well as distractibility, hyperactivity, and other symptoms of attention deficit hyperactivity disorder (ADHD). Many children with SMD receive the diagnosis of bipolar disorder (BD) in the community, although they do not have clear manic episodes (with symptoms such as extreme happiness and decreased need for sleep). Because SMD has not been studied in depth, we do not know which medications are most helpful to those with SMD. This study will evaluate the effectiveness of the stimulant medication methylphenidate (MPH, more commonly known as Ritalin ) when combined (or not combined) with the antidepressant citalopram (Celexa ) in treating symptoms of SMD in children and adolescents. This study will provide information about how to treat SMD in youth. This study will include approximately 80 patients between 7 and 17 years of age with SMD. The patient s symptoms must have started before age 12. The study will consist of four phases carried out over 4 to 5 months. During Phase 1, the patient will undergo blood and urine tests, and will gradually taper off his or her medication. The duration of this phase depends on the patient s medication before starting the study. In Phase 2, the patient remains off all medication for 1 week. In Phase 3, the patient will be treated with MPH for 2 weeks, and then will be randomly assigned to receive either MPH plus citalopram or MPH plus a placebo for a further 8 weeks. In Phase 4, the researchers will evaluate the effectiveness of the medications taken, and begin an open treatment phase using medications that they deem appropriate for that patient (this may include MPH with citalopram and/or other medication combinations). Most patients will be admitted to the Pediatric Behavioral Health Unit at the National Institutes of Health Clinical Center during the medication withdrawal part of the study (Phases 1 and 2). From Phase 3 on, a patient may participate as an inpatient, outpatient, or in day treatment, depending on what is in his or her best interests. ...

NCT ID: NCT00748956 Completed - Anxiety Disorders Clinical Trials

Intranasal Administration of Neuropeptide Y in Healthy Male Volunteers

NPY
Start date: January 2010
Phase: Phase 2
Study type: Interventional

There is growing evidence that neuropeptides act as neuronal messengers in the brain and have diverse functions that may include the regulation of mood and behavior. For example, neuropeptide Y (NPY) is thought to play a role in the adaptive stress response. The therapeutic application of neuropeptides for psychiatric disorders has been limited by difficult and unreliable penetration of the blood-brain barrier (BBB). However, recent data suggest that intranasal administration may provide a means of effectively delivering some of these neuropeptides to the brain. Thus far it is unclear if this is the case for NPY. The aims of this project are: 1. To evaluate, in 15 healthy male volunteers aged 25-45, the effect of intranasal NPY administration (0, 50 and 100 nmol) on its levels in cerebrospinal fluid (CSF), measured by means of lumbar puncture using an intraspinal catheter between L4 and L5, and in plasma, measured using an intravenous catheter in the forearm. One of the three treatments will be administered to each participant in a double-blind fashion. The 0 nmol condition will serve as the placebo control. 2. To test the effect of intranasal NPY administration on mood and anxiety.

NCT ID: NCT00747396 Active, not recruiting - Health Behavior Clinical Trials

The Bucharest Early Intervention Project

BEIP
Start date: September 2000
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the long term effects of early intervention (placement into foster care) on physical, cognitive, social and brain development and psychiatric symptomatology in previously institutionalized children.

NCT ID: NCT00742365 Completed - Depression Clinical Trials

Predicting Effectiveness of Light Treatment for Winter Seasonal Affective Disorder

Start date: November 2007
Phase:
Study type: Observational

This study will evaluate a possible tool for predicting future effectiveness of bright light in treating seasonal affective disorder, winter subtype, and will examine secondary effects of bright light on cardiovascular risk factors.

NCT ID: NCT00741299 Completed - Bipolar Disorder Clinical Trials

A Study of the Association Between Tobacco Smoking and Bipolar Affective Disorder

Start date: August 2007
Phase: N/A
Study type: Observational

The purpose of this study is to examine whether tobacco smoking is associated with bipolar affective disorder (severity of depressive and manic symptoms, presence of psychotic symptoms, history of a suicide attempts and other clinical features.)

NCT ID: NCT00704379 Completed - Clinical trials for Traumatic Brain Injury

Treatment Strategy to Prevent Mood Disorders Following Traumatic Brain Injury

Start date: June 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to examine the efficacy of sertraline to prevent the onset of mood and anxiety disorders during the first six months after traumatic brain injury.

NCT ID: NCT00700609 Terminated - Depressive Disorder Clinical Trials

Family Based Treatment of Depressed Adolescents

BudFam
Start date: June 2008
Phase: Phase 2
Study type: Interventional

The purpose of this project is to assess the effectiveness of a family-based therapy (Attachment based family therapy-ABFT) for Norwegian adolescents (13-17 years) referred to specialist mental heath clinics.

NCT ID: NCT00699218 Completed - Depression Clinical Trials

A Pilot Study on Repetitive Transcranial Magnetic Stimulation (rTMS) Treatment of Bipolar Depression

TMS-BD
Start date: May 2008
Phase: N/A
Study type: Interventional

This is a pilot project to study if repetitive Transcranial Magnetic Stimulation (rTMS) will benefit patients with bipolar depression safely. Based on published studies, this study hypothesizes that rTMS on the left dorsal prefrontal lobe will improve symptoms in some patients who have failed at least two medications.

NCT ID: NCT00683709 Completed - Clinical trials for Schizoaffective Disorder

Specialized Clozapine Clinic for Bipolar and Schizoaffective Disorder

Start date: January 2007
Phase: Phase 4
Study type: Observational

Bipolar Disorder (BD) and Schizoaffective Disorder (SA) clients. - determine if after 12 months of treatment with clozapine, the BMI changes with clients who are councelled as usual regarding weight gain while on Clozapine. - determine if after 12 months of treatment with clozapine, the BMI changes with intense, structured councelling about diet and exercise.

NCT ID: NCT00663871 Completed - Clinical trials for Cardiovascular Diseases

Evaluating the Effects of Omega-3 Fatty Acids on Heart Disease and Behavior

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

Omega-3 fatty acids are a certain kind of fish fat that has recently been shown to have health benefits. This study will examine the effectiveness of fish oil supplementation for reducing the early signs of heart disease risk and for improving mood, impulsivity, and anger levels.