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Hyperkinesis clinical trials

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NCT ID: NCT01705613 Completed - Clinical trials for Attention Deficit/Hyperactivity Disorder

Cost-effectiveness of the Treatment of Attention Deficit/Hyperactivity Disorder With Methylphenidate Immediate-release in Brazil

Start date: April 2014
Phase: N/A
Study type: Observational

The first objective is to measure the QALYs (Quality Adjusted Life Years) of Brazilian children and adolescents, submitted to methylphenidate immediate-release treatment for Attention Deficit Hyperactivity Disorder (ADHD). For this, the Health Utility Index scale (HUI) will be completed by the patient and/or family, in two moments of an observation study with immediate-release methylphenidate: at the baseline and 6th month of treatment in the follow-up. The results provides information to calculate the utility measure and determine the QALYs (Quality Adjusted Life Years). After this, for the cost-effectiveness of the treatment, it will be used a Markov model of decision analysis, and a Monte Carlo simulation with 10,000 random trials. Subjects will be submitted to immediate-release methylphenidate treatment in a maximum dose of 0.5mg/kg/day. The total treatment monitoring is 06 (six) months, and patients will be evaluated at baseline, first, third and sixth month. The HUI rating scales are fulfilled by parents and patients (if >12 years old only) at baseline and 6th month. The period for inclusion of new patients comprises from 01/01/2011 to 31/12/2013.

NCT ID: NCT01694667 Completed - Clinical trials for Autism Spectrum Disorders

Omega-3 Fatty Acids for Hyperactivity Treatment in Autism Spectrum Disorder

Start date: September 2012
Phase: Phase 2
Study type: Interventional

The proposed study is an internet-based, randomized, double-blind, placebo-controlled trial which will assess changes in hyperactivity in children ages five through eight with an autism spectrum disorders (ASD) and elevated levels of hyperactivity. In order to answer this question, this study will assess changes in hyperactivity as measured by the Aberrant Behavior Checklist (ABC) in children with ASD and elevated baseline levels of hyperactivity who are randomly assigned to use 1.3 grams of omega-3 fatty acids daily compared to placebo. The overwhelming majority of study procedures, including recruitment, informed consent, assessment of inclusion and exclusion criteria, and collection of baseline and outcome measures will take place over the internet.

NCT ID: NCT01692782 Completed - Clinical trials for Adult Attention Deficit Hyperactivity Disorder

Adult Attention Deficit Hyperactivity Disorder

Start date: December 2012
Phase: Phase 2
Study type: Interventional

A Phase 2 study of SEP-225289 in adults with attention deficit hyperactivity disorder (ADHD).

NCT ID: NCT01686724 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder Symptoms

Study of the Collaborative Life Skills Program

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

This study tests the effectiveness of a newly developed integrated school-home behavioral intervention for behaviors related to Attention Deficit Hyperactivity Disorder (ADHD). The intervention is implemented by school-based mental health professionals within school settings.

NCT ID: NCT01682915 Completed - Clinical trials for Attention Deficit/Hyperactivity Disorder

Structural and Functional Connectivity of Frontostriatal and Frontoparietal Networks as Endophenotypes of ADHD

Start date: August 1, 2012
Phase:
Study type: Observational

Attention deficit/hyperactivity disorder (ADHD) is a common, impairing, clinically and genetically heterogeneous neuropsychiatric disorder with lifelong executive dysfunctions. The ultimate goal of this 3-year case-control imaging genomic study with unaffected siblings and typically developing (TD) children as controls is to identify useful imaging endophenotype for ADHD by investigating the structural connectivity, as assessed by diffusion spectrum imaging (DSI), and functional connectivity, as assessed by resting-state fMRI (rsfMRI) of brain regions related to cognitive/executive controls with regards to the ADHD status and the presence of dopamine transporter gene variants (DAT1). Specific Aims: 1. to validate the executive functions, visuospatial memory, and structural and functional connectivity in frontostriatal, and frontoparietal circuitries as effective neurocognitive endophenotypes; 2. to correlate the data from structural and functional connectivity, neuropsychology, and ADHD core symptoms stratifying by the presence of ADHD, proband-unaffected sibling dyads, and the presence of DAT1 variant; and 3. To investigate reported candidate genes, in addition to DAT1 variant, related to dopamine and noradrenergic neurotransmitter systems in the association with neurocognitive endophenotypes such as DRD1, DRD2, DRD4, DRD5, DBH, MAO-A, ADRA2A, ADRA2C, NET, and COMT.

NCT ID: NCT01678209 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Imaging Stimulant and Non Stimulant Treatments for ADHD: A Network Based Approach

Start date: October 2012
Phase: Phase 4
Study type: Interventional

The growing number of medications used to treat attention-deficit/hyperactivity disorder (ADHD) raises important questions about whether different medications have similar or different therapeutic mechanisms of action. We have recently shown that the stimulant methylphenidate (MPH) and the non-stimulant atomoxetine (ATX) produce clinical improvement via a common mechanism in motor cortex, and distinct actions in frontostriatal and midline cingulate-precuneus regions. These exciting findings offer a window into the common and unique neurophysiological mechanisms of response to stimulant and non-stimulant treatments. However, the interpretation and clinical utility of these results would be greatly enhanced by in-depth investigation of the impact of the two treatments on relevant neural networks, and analyses which evaluate whether improvement is achieved via normalization or other adaptive changes in brain function.

NCT ID: NCT01677819 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Inhibition Control of Children and Adolescents With ADHD

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

The objectives of this study are to investigate: 1. the effect of methylphenidate on attention; 2. the relations between methylphenidate and inhibition control and working memory; 3. the relations between inhibition control and verbal attention and working memory; 4. the effect of methylphenidate on the changes of neuropsychological functioning and blood pressure.

NCT ID: NCT01675869 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Executive Function/Metacognitive Training for At-Risk Preschoolers

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

The purpose of this study is to see if an intervention training executive functions like attention, working memory, and self-regulation for preschoolers at risk for Attention-Deficit/Hyperactivity Disorder is feasible, acceptable to families, and improves attention, behavior, and functioning.

NCT ID: NCT01675804 Completed - Clinical trials for Attention Deficit Disorder With Hyperactivity

Computer-assisted Cognitive Rehabilitation (CACR), Placebo CACR and Psycho-stimulants in the Treatment of ADHD

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

Current research aimed to compare the efficacy of computer-assisted cognitive rehabilitation (CACR), stimulant drugs and Placebo CACR on executive functions and clinical symptoms of children with attention deficit/hyperactivity disorder (ADHD).

NCT ID: NCT01660464 Completed - Clinical trials for Attention-Deficit/Hyperactivity Disorder

Guided Self-Help for Parents of Adolescents With Attention-Deficit/Hyperactivity Disorder (ADHD)

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

Cognitive-behavioral based guided self-help for parents of adolescents with Attention-Deficit/Hyperactivity Disorder (ADHD) is investigated in a feasibility and effectiveness study. The treatment is offered under routine-care conditions of the health-care system in Germany. Practicability, treatment participation and effectiveness is documented and tested in a one-group pre-test/post-test design.