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NCT ID: NCT01463111 Completed - Bipolar Disorder Clinical Trials

Decision-Making in Bipolar Disorder

Start date: May 2011
Phase: N/A
Study type: Interventional

Forty subjects with bipolar disorder who are not receiving a mood-stabilizing medication for the treatment of their illness will participate in this study. The study aims to evaluate how decision-making is affected by treatment for bipolar disorder. Prior to beginning treatment, patients will complete questionnaires and a one-hour computer-administered assessment of decision-making. Differences between pre-post decision-making outcomes will be evaluated to examine whether the neuroeconomic concepts of risk aversion, loss aversion, risk tolerance and delay discounting are affected by treatment. The overall goal of this study will be to identify whether decision-making in people with bipolar disorder is affected by treatment. Specifically the investigators will compare decision-making characteristics among bipolar patients prior to treatment with how these decision-making characteristics change over the course of 6 weeks of standard medication therapy for bipolar disorder. A total of 6 decision-making tasks and one control task will be administered via computer to eligible subjects. The investigators will evaluate decision-making under varying conditions of reward, risk, and uncertainty and over time. The investigators hypothesize that decision-making will improve across these assessments after 6 weeks of treatment.

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: NCT01459705 Completed - Clinical trials for Post-Traumatic Stress Disorder

Comparing Virtual Reality Exposure Therapy to Prolonged Exposure

VRPE Extension
Start date: October 2011
Phase: N/A
Study type: Interventional

This study is evaluating the efficacy of virtual reality exposure therapy (VRET) by comparing it to prolonged exposure therapy (PE) and a waitlist(WL) group for the treatment of post traumatic stress disorder (PTSD) in active duty (AD) Soldiers with combat-related trauma. The investigators will test the general hypothesis that 10 sessions of VRET or PE will successfully treat PTSD, therapeutically affect levels of physiological arousal, and significantly reduce perceptions of stigma toward seeking behavioral health services.

NCT ID: NCT01458340 Completed - ADHD Clinical Trials

A Study of TD-9855 in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)

Start date: December 2011
Phase: Phase 2
Study type: Interventional

The safety and efficacy of multiple dosages of TD-9855, administered once daily, will be evaluated in adult males with ADHD.

NCT ID: NCT01457677 Completed - Clinical trials for Major Depressive Disorder

ARTDeCo Study: A Study of RO4995819 in Patients With Major Depressive Disorder And Inadequate Response to Ongoing Antidepressant Treatment

Start date: December 2011
Phase: Phase 2
Study type: Interventional

This multi-center, randomized, double-blind, placebo-controlled, parallel-group study will investigate the efficacy and safety of RO4995819 as adjunctive therapy in patients with major depressive disorder having inadequate response to ongoing antidepressant treatment. Patients will be randomized to receive once daily doses of 5 mg, 15 or 30 mg of RO4995819 or matching placebo. The anticipated time on study treatment is 6 weeks.

NCT ID: NCT01457404 Completed - Clinical trials for Substance-Related Disorders

Integrated Cognitive Behavioral Therapy (ICBT) for Posttraumatic Stress Disorder (PTSD) and Substance Use Disorders

Start date: February 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the safety and practicality, feasibility and efficacy of ICBT for co-occurring PTSD and substance use disorders within the OEF/OIF/OND Veterans population, as delivered by routine clinicians at the Veterans Affairs.

NCT ID: NCT01457391 Completed - Clinical trials for Substance-Related Disorders

Cognitive Behavioral Therapy (CBT) for Posttraumatic Stress Disorder (PTSD) in Community Addiction Treatment

Start date: December 2010
Phase: Phase 3
Study type: Interventional

The purpose of this phase of the study is to assess the efficacy of CBT for PTSD, as delivered by routine addiction counselors in community treatment programs, and to compare CBT for PTSD with both Individual Addiction Counseling (IAC) and Treatment as Usual (TAU) on the primary outcomes.

NCT ID: NCT01457235 Completed - Bipolar Disorder Clinical Trials

The Effects of Cognitive Remediation on Cognitive Function in Remitted Bipolar Disorder - a Proof of Concept Study

REMEDI
Start date: August 2011
Phase: N/A
Study type: Interventional

Cognitive remediation (CR) is a new psychological treatment, which aims to improve cognitive function and coping skills. Several studies have recently demonstrated that CR improves cognitive and occupational function in patients with schizophrenia and with depression (e.g. Wykes et al 2007, Elgamal et al 2007). However, it is unclear whether CR improves cognitive and socio-occupational function in individuals with bipolar disorder (BD) and, if so, what impact this might have on these people's abilities in terms of work, coping strategies, quality of life, and everyday safety. The aim of the present PhD study is to investigate if CR has beneficial effects on cognitive and socio-occupational function in patients with previous mania and depression who experience persistent cognitive difficulties. Such effects would suggest implementation of CR in future treatment of bipolar disorder in order to facilitate the patients' ability to cope with the responsibilities related to work and everyday life. The hypotheses of the present study are that CR (in comparison to standard treatment) will 1) improve verbal learning and recall; and 2) improve sustained attention, executive function and psychosocial function.

NCT ID: NCT01456338 Completed - Clinical trials for Substance-Related Disorders

Cognitive Behavioral Therapy for Post Traumatic Stress Disorder in Addiction Treatment

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

The purpose of this phase of the study is to further assess the efficacy of cognitive behavioral therapy (CBT) for posttraumatic stress disorder (PTSD), as delivered by routine addiction counselors, and to compare CBT for PTSD with individual addiction counseling (IAC) on our primary outcomes.

NCT ID: NCT01454635 Completed - Clinical trials for Major Depressive Disorder

Analisis of Facors Involved in Antidepressant Treatment Response of Major Depressive Disorder

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

The purpose of this study is to predict and visualize sertraline treatment response in major depressive disorder with clinical symptoms, demographic and stress state, personality, eight genetic polymorphisms at baseline.