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Mood Disorders clinical trials

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NCT ID: NCT01559857 Recruiting - Clinical trials for Major Depressive Disorder

Pioglitazone in Patients With Mood Disorders

Start date: November 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to see how an insulin sensitizing medication, Pioglitazone, can cause changes in mood in some depressed patients. Study participants receive assessment of their cognitive and metabolic functioning. If they meet criteria, they will be asked to take either Pioglitazone or a placebo for a 90-day trial. Participants will undergo an Oral Glucose Tolerance Test to measure fasting insulin and glucose levels, as well as routine blood testing. The investigators hope to quantify the role of Pioglitazone in patients with mood disorders and compare the values to those previously obtained in a healthy age-matched control population. The investigators also hope to examine the association between IR and cognitive performance and clinical course of depression in patients with mood disorders.

NCT ID: NCT01557192 Suspended - Bipolar Depression Clinical Trials

Low Field Magnetic Stimulation (LFMS) in Mood Disorders: 6 Treatments

LFMS6tx
Start date: May 2010
Phase: Phase 1
Study type: Interventional

To demonstrate the efficacy of multiple applications of Low Field Magnetic Stimulation (LFMS) as an antidepressant treatment in subjects with mood disorders.

NCT ID: NCT01547026 Completed - Schizophrenia Clinical Trials

Self-regulation Strategies to Improve Exercise Behavior Among Schizophrenic Patients

Start date: April 2012
Phase: N/A
Study type: Interventional

Patients who suffer from diseases of the schizophrenia spectrum are frequently burdened by weight gain. Sport programs have been shown to improve somatic and psychological health. However, the motivation to participate in sports therapy is usually impaired due to illness-related factors such as anhedonia and negative symptoms. Previous attempts to increase participation in sports therapy have used psycho-educational and behavioral attempts that require a lot of resources. In this study the investigators will use a brief method developed in experimental social psychology to build up implementation intentions. This method has been shown to improve psychological test performance in schizophrenia patients but has never been used in a clinical context. In two psychiatric hospitals, in-patients with schizophrenia who have been examined by a medical doctor, for whom any medical concerns for sports therapy participation have been excluded and who declared their motivation to participate in an existing standard sports exercise program will be recruited for the study. After information on the study and signing of an informed consent patients will be randomly assigned to two treatment conditions. In the control condition, the main therapist will individually deliver a 10-minute psycho-education on the helpfulness of sports to improve the health; this will be repeated in a shorter form in the regular individual treatment sessions over the following weeks. The intervention condition will use a structured procedure of the same duration to build up implementation intentions to participate in the sports therapy. The implementation intentions will briefly be repeated and updated in the following session. Primary outcome variables will be percentage of attended sport therapy sessions, persistence and compliance. Secondary outcome variables will be Body Mass Index. As confounding variables the investigators will assess amount of anti-psychotic medication in Chlorpromazine equivalents, negative and depressive symptoms, usual sport activities and cognitive impairments. The investigators expect that building up implementation intentions will increase participation, persistence and compliance of the patients in the sports and exercise therapy program compared to the patients who just have received psycho-education.

NCT ID: NCT01533064 Completed - Mood Disorders Clinical Trials

Response of Psychiatric Outpatients to the Great East Japan Earthquake

Start date: March 2011
Phase: N/A
Study type: Observational

Objective: Reports have described how hospitalized psychiatric patients respond to disasters; however, few reports have described the response to disaster among psychiatric outpatients, who have relatively mild disease in comparison with hospitalized, severely ill psychiatric patients. Here the investigators have analyzed the response to disaster among this under-studied population. Method: The Great East Japan Earthquake on March 11, 2011, was a catastrophic disaster. The investigators studied psychiatric change among a population of psychiatric outpatients in Tochigi prefecture, located ~160 km (~100 miles) southeast of the Fukushima nuclear power plant, in an area that suffered moderate damage from the earthquake. A total of 328 psychiatric outpatients were enrolled and were grouped into the diagnostic categories F2 (schizophrenic, schizotypal, and delusional disorders), F3 (affective disorders), and F4 (neurotic, stress-related, and somatoform disorders). All diagnoses were made using International Classification of Diseases (ICD) 10 criteria. Changes in symptoms were measured as a change in psychotropic medication after the disaster.

NCT ID: NCT01518049 Completed - Clinical trials for Affective Disorders, Psychotic

Clinical Validation of the Rating Scale for Psychotic Depression (RAS-PD)

Start date: February 2012
Phase: N/A
Study type: Observational

The aim of this study is to develop a scale to measure the severity of depression with psychotic symptoms (psychotic depression). Furthermore, we hope to detect potential biomarkers (substances in the blood) which can aid in the detection of psychotic depression. Main hypothesis: A clinically valid rating scale measuring the severity of psychotic depression can be developed.

NCT ID: NCT01493323 Terminated - Suicide, Attempted Clinical Trials

Functional Imaging of Psychic Pain

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

Suicidal behaviour (SB) represents a major public health problem, costing life in more that one million people every year worldwide. Even if SB is considered as a consequence of social adversity and depression, these stress factors are often necessary but not sufficient to explain the occurrence of a suicidal act. A preliminary study suggests that an increased perception of psychic pain during a major depressive disorder increases the risk of suicide behaviour. The investigators aimed to investigate the relationship between social exclusion (a classic trigger of psychic pain) and SB and improve our knowledge about the physiopathology of this domain.

NCT ID: NCT01473550 Completed - Mood Disorder Clinical Trials

Mental Health Engagement Network (MHEN)

MHEN
Start date: November 2011
Phase: N/A
Study type: Interventional

Patients with mood disorder or psychotic disorder will be given handheld devices with personal health records to educate, monitor and deliver customizable healthcare tools based on their personal needs. The use of technology has great potential to deliver care more effectively and efficiently. No actual information is on the handheld device - it is accessed from a secure site behind hospital firewalls.

NCT ID: NCT01462305 Completed - Clinical trials for Seasonal Affective Disorder

30-Minute Light Exposure for the Treatment of Seasonal Affective Disorder

SAD
Start date: January 6, 2012
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the effect of light therapy using a narrow 467nm light compared to a 580nm light in subjects with Seasonal Affective Disorder (SAD). It is hypothesized that the 467nm light will improve the symptoms of SAD better than the 580nm light.

NCT ID: NCT01462058 Completed - Mental Health Clinical Trials

The Role of Vitamin D Supplementation on Well Being and Symptoms of Depression During the Winter Season in Health Service Staff

D3-vit-SAD
Start date: October 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate whether vitamin D3 (70 micrograms) is better than placebo in preventing depression symptoms among employees in health care

NCT ID: NCT01431092 Completed - Schizophrenia Clinical Trials

Melatonin Versus Placebo for Benzodiazepine Discontinuation in Patients With Schizophrenia

SMART
Start date: October 2011
Phase: Phase 4
Study type: Interventional

In this trial, researchers aim to investigate if prolonged-release melatonin can facilitate the withdrawal of chronic benzodiazepine administration in patients with schizophrenia. Furthermore, researchers will investigate the association of benzodiazepine dose reduction with the following clinically important variables: sleep, psychophysiology, cognition, social function, and quality of life.