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Hyperkinesis clinical trials

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NCT ID: NCT03006367 Completed - Clinical trials for Attention Deficit Disorder With Hyperactivity

Pharmacokinetic and Tolerability Study of NFC-1 in Subjects Aged 6-17 Years With ADHD

Start date: January 7, 2017
Phase: Phase 1
Study type: Interventional

This is a open-label, single ascending dose, pharmacokinetic, and tolerability study of NFC-1 in Children and Adolescents (Ages 6-17 Years) with ADHD.

NCT ID: NCT02959528 Completed - Clinical trials for Attention Deficit Disorder With Hyperactivity

The Effects of Working Memory Training in Children With Attention-Deficit/Hyperactivity Disorder

Start date: October 2015
Phase: N/A
Study type: Interventional

Previous studies indicated that children with attention-deficit/hyperactivity disorder (ADHD) often suffer from deficits in executive function, such as attentional control, inhibition, and working memory. One of these executive functions, working memory, plays a critical role in academic performance and classroom behavior. Working memory is essential for performing complex cognitive tasks such as comprehension, learning, and reasoning. Several studies have shown that training of working memory has positive effects for ADHD and other cognitive disorder in children. However, transfer effects across studies appear to be variable and inconsistent. Event-related potentials can be a useful tool to gain insights into such mechanism. Therefore, the aim of the present study is to investigate both near and far transfer effects of N-back training in children with ADHD. In addition, the recording and analysis of event-related potentials will be adopted while children with ADHD perform the complex visuo-spatial and phonological working memory tasks.

NCT ID: NCT02951754 Recruiting - Clinical trials for Attention Deficit Disorder With Hyperactivity

Methylphenidate in Adults With Attention Deficit/Hyperactivity Disorder

Start date: February 2002
Phase: Phase 4
Study type: Interventional

Methylphenidate (MPH) is the first-line pharmacological treatment for adults with Attention-Deficit/Hyperactivity Disorder (ADHD). Nevertheless, there is considerable interindividual variability regarding the dose required, tolerability and response rates to MPH. The aim of this study is to address the clinical and genetic predictors of MPH treatment outcomes in ADHD.

NCT ID: NCT02942225 Completed - Clinical trials for Attention-deficit/Hyperactivity Disorder

The Metabolome Profiling and Pathway Analysis of ADHD

Start date: August 1, 2016
Phase:
Study type: Observational

The purpose of this study is to understand the pathophysiological mechanisms of ADHD, especially the metabolomic pathway related to the behavioral/neuropsychological deficits of ADHD. To identify specific metabolites that show significant differences between ADHD and control groups, both liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry will be performed. In addition, the behavioral measures include ADHDRS-IV, SNAP-IV, CBCL, CGI-ADHD-S, SAICA, and Family APGAR-C. Neuropsychological testing, including CPT and CANTAB, will be performed. Conditional logistic regression and partial least squares discriminant analysis will be applied to identify significant metabolites for ADHD. Pathway enrichment and topology analyses will be conducted to evaluate the regulated pathways.

NCT ID: NCT02937142 Completed - Clinical trials for Attention Deficit Disorder With Hyperactivity

Cognitive Behavior Group Therapy in Adolescents With Attention Deficit Hyperactivity Disorder

Start date: January 2017
Phase: N/A
Study type: Interventional

Attention Deficit Hyperactivity Disorder (ADHD) is a neurodevelopmental disorder which starts in childhood and is characterized by symptoms of attention deficit, hyperactivity and impulsivity. Persistence into adolescence is frequently associated with among other low educational achievement, interpersonal difficulties, anxious and depressive symptoms and sleep problems. Treatment guidelines recommend psychological treatment as part of the treatment plan, however compared to children and adults, there is still a substantial lack of knowledge about appropriate psychological treatment in adolescents. The present study examines a psychological intervention for adolescents with ADHD, cognitive behavior group therapy. The intervention consists of 12 weekly cognitive behavioral therapy sessions addressing core difficulties and concerns of the adolescent population with ADHD. The investigators wish to determine the efficacy of group therapy in adolescents with ADHD who receive medical treatment but still have impairing ADHD symptoms.

NCT ID: NCT02918214 Completed - Septic Shock Clinical Trials

Prognostic Assessment of Diastolic and Systolic Left Ventricular Function in Septic Shock

PRODIASYS2
Start date: January 2017
Phase:
Study type: Observational

Sepsis induces a reversible systolic and diastolic cardiac dysfunction. The presence of a left ventricular (LV) diastolic dysfunction during septic shock could favor harmful volume overload. Recently, a meta-analysis suggested a negative prognostic role of LV diastolic dysfunction in septic patients (Od Ratio: 1.82; 95%CI: 1.12 - 2.97; p = 0.02) but its external validity is hampered by the numerous limits and the heterogeneity of the studies. To date, a pathophysiological link between LV diastolic dysfunction associated with septic shock and the water balance (reflecting volume overload) remains to establish. In addition, small size studies reported an excess of mortality in patients with septic shock who were diagnosed with a high cardiac output. However, no large cohort has yet confirmed the negative prognostic role of a hyperkinetic hemodynamic profile at the initial phase of septic shock.

NCT ID: NCT02911194 Completed - Clinical trials for Autism Spectrum Disorder

a2 Milk for Autism and Attention-deficit Hyperactivity Disorder (ADHD)

A2MT
Start date: September 2016
Phase: N/A
Study type: Interventional

Under double-blind, placebo-controlled, cross-over conditions, the short-term effects of use of A1 beta casein free milk (a2 milk) and milk containing A1 beta casein will be compared in a sample of pre-pubescent boys diagnosed with an autism spectrum disorder (ASD) with concurrent features of attention-deficit hyperactivity disorder (ADHD).

NCT ID: NCT02908802 Active, not recruiting - Clinical trials for Attention Deficit Hyperactivity Disorder (ADHD)

Probiotic Supplement as Treatment for Students With ADHD

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

Subjects will answer the following questionnaire and tests: - Symptom severity and improvement will be measured using ADHA Rating scale IV (ADHD RS) - Demographic Questionnaire - composed by the researchers - Family Eating Habits Questionnaire (FEAHQ-33) - Food Frequency Questionnaire (FFQ) - Test MOXO The subjects will take the study product for six months. After six months the subject will fill once again all the questionnaires.

NCT ID: NCT02889354 Completed - Clinical trials for Attention Deficit Disorder With Hyperactivity

Group-based Cognitive-behavioral Therapy for Adults With Attention-deficit/Hyperactivity Disorder Inattentive-type

Start date: August 2016
Phase: N/A
Study type: Interventional

The newly developed CBT for ADHD inattentive-type (ADHD-I) protocol is tested for feasibility and acceptability in a pilot study with a single group design. The study also evaluates measurements and recruiting possibilities, and effects of the intervention. Research hypotheses include: 1. There is a basis for recruiting ADHD-I patients for participation in an RCT at psychiatric outpatient units, 2. The measurements in the study are feasible and reasonable in regards to patient characteristics; that is, the patients are responding to the questionnaires as intended, 3. The CBT for ADHD-I intervention is feasible in terms of treatment completion, compliance to home assignments, and credibility and relevance, and is lacking of or involves a tolerable degree of adverse effects, and 4. The CBT for ADHD-I protocol reduces core symptoms of ADHD-I as well as symptoms of stress, depression, and anxiety, and improves quality of life.

NCT ID: NCT02874690 Completed - Clinical trials for Autism Spectrum Disorder

Eye Tracking as a Predictor of Methylphenidate Response in Autism With ADHD

SAT
Start date: February 19, 2016
Phase: Early Phase 1
Study type: Interventional

The overall goal of this research is to use neurophysiological measures to profile strengths and deficits for Attention Deficit Hyperactivity Disorder co-morbidity in Autism Spectrum Disorder to clarify diagnosis and to predict treatment response.