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Mood Disorders clinical trials

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NCT ID: NCT01842217 Terminated - Postmenopausal Clinical Trials

Validation of [18F]FES for Imaging of Brain Estrogen Receptors

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

Validation of [18F]-FES for imaging of estrogen receptors in the brain The primary objective of the study is to determine if [18F]-FES Positron Emission Tomography (PET) can be used to quantify the estrogen receptor expression in the human brain.

NCT ID: NCT01830088 Terminated - Depressive Disorder Clinical Trials

Family Based Treatment of Depressed Adolescents (AHUS)

BudFam2
Start date: October 2013
Phase: N/A
Study type: Interventional

Major depressive disorder (MDD) affects about 5% of adolescents and is on the rise both internationally and in Norway. Further, it is also associated with increased risk for suicide. Not surprisingly, depression is the largest reason for referral to specialty mental health services for adolescents (13-17 years) in Norway. Although anti-depressants and Cognitive behavioral therapy are strong treatments and have received extensive research, the best treatments show a recovery rate of only 37 %. There is a need to develop and test alternative treatments that can stand alone or augment anti-depressant medication. Family factors play an important role in the etiology, maintenance and relapse of depression. A promising family-based treatment (Attachment based family therapy- ABFT) was imported to Norway and its feasibility tested in a pilot randomized clinical trial with 20 families. The results showed promising treatment outcomes. Although the developers of the model have refined, adapted the model to suicidal ideation and built strong technology to support dissemination, a definitive study of ABFT for adolescents with major depression has not yet been conducted. Therefore the primary aim of this study is to test if ABFT is more effective that enhanced usual care (EUC) to treat clinic-referred adolescents with major depression. The investigators will test the hypothesis that 12 weeks of ABFT therapy will produce a greater proportion of adolescents report remission from depression and symptom change than 12 weeks of enhanced clinical care (EUC). Secondary research aims are i) to test a hypothesis that parent-adolescent conflict will be more sensitive to change for adolescents receiving ABFT that adolescents receiving EUC ii) to explore patterns of change in suicidal ideation in the recruited sample in the acute-phase treatment. Central challenges to the study are i) blinding therapists/patients, which is difficult in psychotherapy trials ii) lack of a standardized control condition, and iii) selecting and training regular staff therapists to high adherence levels. However, with tighter control over these factors than is normal for a typical effectiveness trial, the investigators expect results to show what to expect under the "best of conditions" in community clinics. Benchmark derived from the study will inform how to effectively train therapists and subsequently implement the model into mainstream services.

NCT ID: NCT01820286 Completed - Depression Clinical Trials

Positive Psychology for Mood Disorders

PPBPAD
Start date: March 2013
Phase: N/A
Study type: Interventional

The investigators are doing this study to see if "positive psychology" can help adults with depression or bipolar disorder. Positive psychology involves exercises—short tasks—that try to increase good feelings and emotions, like optimism, happiness, personal strengths, and well-being. Positive psychology exercises might include imagining a bright future, being grateful for good events, forgiving others, and doing kind acts for others. The investigators want to see if practicing positive psychology exercises after leaving the hospital can increase feelings of hope, optimism, and positive thinking. The investigators are asking you to take part in this research study because you are in the hospital for depression or bipolar disorder. This research study will compare "positive psychology exercises" to "control condition exercises." During the study, you may take part in control condition exercises instead of positive psychology exercises.

NCT ID: NCT01818453 Completed - Clinical trials for Major Depressive Disorder

Can Genetics Predict Treatment Response to a Computerized Self-help Program for Depression?

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

The goal of this project is to determine whether genetic information can be used to predict response to an internet-based treatment of depression. Several studies now indicate that completing an internet-based treatment for depression, called Deprexis, can significantly improve symptoms of depression. However, not everyone improves. The purpose of this study is to determine whether genetic profile can predict who is likely to improve.

NCT ID: NCT01816087 Completed - Osteoporosis Clinical Trials

Performances of a Brief Assessment Tool for the Early Diagnosis of Geriatric Syndromes by Primary Care Physicians

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

The AGE (Active Geriatric Evaluation) aims to develop a brief assessment tool adapted to the primary care setting.

NCT ID: NCT01815398 Completed - Anxiety Disorders Clinical Trials

Cognitive Skills Training for Homeless Youth

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

Many young people who are homeless have cognitive deficits which impede their ability to secure and maintain employment. This study looks to see if targeting cognitive deficits can improve cognition and vocational outcome.

NCT ID: NCT01784705 Completed - Clinical trials for Seasonal Affective Disorder (SAD)

Transcranial Bright Light Therapy in Seasonal Affective Disorder (SAD)

SAD3
Start date: January 2013
Phase: N/A
Study type: Interventional

Bright light therapy (BLT) has been found to be effective in treatment of seasonal affective disorder (SAD). The mechanism of action of conventional BLT in the treatment of SAD is under debate. Recently, transcranial bright light (TBL) via ear canals has been proved to modulate the neural networks of the human brain and improve cognitive performance in healthy subjects. Moreover, TBL has been found to alleviate symptoms of SAD in open trial. In this case the investigators will study the effect of transcranial bright light treatment via ear canals on depressive and anxiety symptoms in patients suffering from SAD in randomized controlled double-blind study design.

NCT ID: NCT01769859 Terminated - Clinical trials for Major Depressive Disorder

Systematic Genetic Analysis of Phenomenology and Treatment Response in Mood Disorders

Start date: January 2013
Phase:
Study type: Observational [Patient Registry]

The primary goals of this work are: a) to establish a unique collection of mood disorder patients across the life cycle, including children, adults and geriatric patients, with well-defined medical co-morbidities and medication treatment outcomes at the University Hospitals Case Medical Center Department of Psychiatry; b) to establish a collection of nuclear families, including both mothers and fathers, of children diagnosed with mood disorders; c) to perform a systematic genetic analysis of the proposed sample repository to identify genes and genetic variants contributing to inter-patient variability in clinical phenotypes and treatment responses. Our primary hypothesis is that genetic variations may underlie individual variability in disease susceptibility, clinical phenotypes and treatment safety, tolerability, and effectiveness.

NCT ID: NCT01754532 Completed - Schizophrenia Clinical Trials

Correlation Between Clinical Deterioration in Schizophrenic Patients and Hair Cortisol Levels

Start date: January 2013
Phase:
Study type: Observational

The importance of stress as a possible deteriorating factor for schizophrenic patients is well documented. However, this notion is based on subjective experience and retrospective psychological analysis. A novel method of measuring cortisol using hair has a proven correlation to subjective stress in non-clinical as well as psychiatric clinical populations. This pilot study will attempt to assess the use of cortisol hair level, as a marker of stress, to predict clinical deterioration in schizophrenic patients.

NCT ID: NCT01746303 Completed - Mood Disorders Clinical Trials

Omega-3 and Blueberry Supplementation in Age-Related Cognitive Decline

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

The aim of this study is to determine the efficacy of 6 months' dietary supplementation with omega-3 fatty acids and whole freeze dried blueberry powder in improving cognition in older adults. The effects of each of these interventions alone will also be assessed in order to determine whether the combined treatment confers synergistic or additive benefit relative to the effect of each therapy.