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NCT ID: NCT03118011 Recruiting - Clinical trials for Substance Use Disorders

Substance Use Disorders and Tobacco Habits

Start date: April 10, 2017
Phase: N/A
Study type: Interventional

In the department for substance use disorders at Uppsala University Hospital there are two wards. One that is locked, where the patients that are emitted can not go out to smoke and another ward where there is a possibility to go out and smoke during the day. The smoking habits on those two floors will be compared and how they feel about smoking will be evaluated when they are admitted to the ward, at discharge, after 1 mont and after 6 months.

NCT ID: NCT03116620 Completed - Clinical trials for Mastication Disorder

Chewing Function in Pediatric Neuromuscular Disorders

Start date: May 15, 2017
Phase: N/A
Study type: Interventional

We aimed to evaluate chewing function (CF) in children with neuromuscular disorders, and investigate reliability of the Karaduman Chewing Performance Scale (KCPS).

NCT ID: NCT03116165 Terminated - Clinical trials for Post Traumatic Stress Disorder

Cognitive-Behavioural Therapy as a Preventive Treatment for Post Traumatic Stress Disorder

Start date: April 18, 2017
Phase: N/A
Study type: Interventional

This study will examine the use of modified prolonged exposure therapy in trauma patients recently exposed to trauma in an emergency room to prevent the onset of post-traumatic stress disorder.

NCT ID: NCT03115671 Completed - Clinical trials for Autism Spectrum Disorder

Efficacy Study of Vayarin in Children With Autism and Comorbid Attention Deficit Hyperactivity Disorder (ADHD)

Start date: November 30, 2016
Phase: N/A
Study type: Interventional

This research study is carried out to examine the effects of Phosphatidylserine-Omega 3 supplements (i.e., Vayarin) among children with Autism Spectrum Disorder (ASD) and ADHD. Participants will be randomised either to receive the Vayarin treatment (Intervention group) or to a Control group.

NCT ID: NCT03114891 Completed - Clinical trials for Major Depressive Disorder

Accelerated TMS to a Novel Brain Target in MDD and PTSD

Start date: April 20, 2017
Phase: N/A
Study type: Interventional

This is a Clinical Trial designed to evaluate novel transcranial magnetic stimulation (TMS) methods for treating depression/PTSD. TMS is an FDA-approved procedure for treatment-resistant depression. The use of the stimulation in this current study is considered experimental. The purpose of this research study is to compare the effects of TMS at two different brain regions. This information will help the investigators to determine which treatment strategies provide the greatest clinical benefit to patients. Results of the study will provide brain and behavior measures for future work, which may be critical to developing effective disease markers and novel treatments for psychiatric conditions.

NCT ID: NCT03114748 Active, not recruiting - Clinical trials for Psychiatric Disorder

Electroencephalographic Monitoring in Patients Treated by Deep Brain Stimulation

EEG-DBS
Start date: May 2012
Phase: N/A
Study type: Interventional

This protocol aims to develop the use of behavioral and electroencephalographic measures during cognitive tasks in patients treated with deep brain stimulation during the stimulation parameters adjustments. The main clinical goal of this protocol is to find behavioral and or electroencephalographic markers to evaluates the right targeting of stimulation electrodes. On the more fundamental point of view, the study of those data can be used to understand better the action mechanisms of deep brain stimulation.

NCT ID: NCT03114423 Recruiting - Clinical trials for Substance Use Disorders

Eye Movement Desensitization and Reprocessing (EMDR) as a Treatment of Substance Use Disorders

Start date: April 7, 2017
Phase: N/A
Study type: Interventional

The purpose of this clinical study is to examine the established, therapeutic EMDR intervention for patients with substance use disorders (SUD). The EMDR method is an integrative and structured therapeutic method which assumes that memories which have been dysfunctionally stored can lead to harmful behavior. The EMDR protocol used for this clinical trials has been specifically developed for patients with SUD - the results should be compared with traditional therapy. For the assessment of the EMDR treatment some questionnaires are given at several times.

NCT ID: NCT03114007 Recruiting - Quality of Life Clinical Trials

Integrated Prevention and Collaborative Care for Youth Mental Health

Start date: April 24, 2017
Phase: N/A
Study type: Interventional

Mental health problems affect 10-20% of children and adolescents worldwide, with half of affected youth experiencing problems by the age of 14. Despite the early onset of mental health problems, evidence-based prevention and early intervention programs remain scarce. If left untreated, early-onset mental health problems can progress to become severe or chronic conditions, and incur significant medical and societal costs. The current project proposes an integrated screening and intervention model that was developed involving active youth, family and community engagement. This project, known as Inter-Venture, focuses on reducing barriers to youth mental health care and promoting early screening and intervention by fostering collaboration between school and community-based services providers. The Inter-Venture project is being conducted in the Montreal area (Canada), and consists of three intervention modalities. Namely, 1) systematic school-based screening and personality-targeted interventions for students most at risk of mental health problems and substance misuse (the Preventure program); 2) a parent program designed to strengthen parenting skills and to improve the management of child behavior problems (Cope/EQUIPE program); 3) integrated services provided by a multidisciplinary team of professionals (referred to as Inter-Action) for youth with significant symptoms of mental health problems, substance misuse and/or psychosocial difficulties. The intervention model involves knowledge transfer to boost capacity-building and improve the provision and sustainability of evidence-based interventions in community settings. The primary goal of the Inter-Venture trial is to assess the potential effect of the school-based targeted interventions and collaborative care in the prevention, early detection and reduction of mental health problems, substance misuse and psychosocial difficulties among young people. The secondary goal is to assess the effect of interventions on school performance and whether the interventions can protect cognitive functions that may be negatively affected by early-onset substance use and mental health problems, and promote cognitive development through the prevention of these difficulties.

NCT ID: NCT03113682 Active, not recruiting - Rumination Disorder Clinical Trials

A Study of Cognitive-Behavioral Therapy for Rumination Disorder

CBT-RD
Start date: April 1, 2017
Phase: N/A
Study type: Interventional

The primary aim of this study is to pilot cognitive behavioral therapy (CBT-RD) for 10 individuals ages 10 and older who have rumination disorder

NCT ID: NCT03112746 Completed - Clinical trials for Developmental Coordination Disorder

Efficacy of the CO-OP Approach With Brazilian Children With Developmental Coordination Disorder

Start date: March 26, 2009
Phase: N/A
Study type: Interventional

Children with Developmental Coordination Disorder (DCD) have difficulties performing daily activities which reflects negatively on participation, impacting their lives. To date, there are a number of interventions to improve performance of these children on activities they want or need to. In Brazil, there is little research on the efficacy of such approaches. Our main objective was to start a set of studies to examine the effects of the Cognitive Orientation to Daily Occupational Performance Approach (CO-OP Approach) protocol on occupational performance and satisfaction of Brazilian children who have DCD; to examine whether children were able to transfer strategies and skills learned during CO-OP to untrained goals.