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Impulsivity clinical trials

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NCT ID: NCT03844607 Active, not recruiting - Clinical trials for Traumatic Brain Injury

Combined tDCS and Cognitive Training to Reduce Impulsivity in Patients With Traumatic Brain Injury

Start date: January 8, 2019
Phase: N/A
Study type: Interventional

Behavioral changes following a traumatic brain injury (TBI) are one of the biggest challenges for patients, as well as their family members and others involved in their recovery. One of the most common behavioral changes following TBI is the emergence of impulsive behavior, which has been associated with destructive, suicidal, and aggressive behavior, and is related to poor rehabilitation program adherence. The primary objective of this study is to investigate the effect of a novel neuroplasticity based intervention that combines cognitive training and transcranial direct current stimulation (tDCS) to reduce impulsivity and to improve outcomes and quality of life for those who have suffered a TBI.

NCT ID: NCT03623477 Completed - Schizophrenia Clinical Trials

Can Cognitive Training Decrease Reactive Aggression?

Start date: August 16, 2016
Phase: N/A
Study type: Interventional

The purpose of the study is to examine the effects of cognitive training on emotion regulation, impulse control, and aggression in people with schizophrenia. The study compares a combination of computerized cognitive remediation and social cognition training (CRT+SCT) to cognitive remediation alone (CRT). Study outcomes include multiple measures of aggression, emotion regulation, impulse control, cognition, and symptoms.

NCT ID: NCT03457402 Recruiting - Impulsivity Clinical Trials

Shaping Tolerance for Delayed Rewards

DelTA
Start date: September 12, 2017
Phase: N/A
Study type: Interventional

Deficits in self-control are of major public health relevance as they contribute to several negative outcomes for both individuals and society. For children, developing self-control is a critically important step toward success in academic settings and social relationships, yet there are few non-pharmacological approaches that have been successful in increasing self-control. We found in our earlier studies that self-control can be increased in preschool-aged children with high impulsivity by using games in which they practice gradually increasing wait-time for larger, more delayed rewards. We are performing this current study to test if this training to increase self-control can be increased using mobile app technology, with computerized game time being used as a reward.

NCT ID: NCT02930642 Completed - Obesity Clinical Trials

Food Insecurity, Obesity, and Impulsive Food Choice

FIOI
Start date: May 31, 2017
Phase: N/A
Study type: Interventional

The objective of this study is to determine the relations among food insecurity status, obesity, and impulsive food choice patterns and to test the extent to which a mindful eating strategy reduces impulsive choice for food. The central hypothesis is that food-insecure individuals will demonstrate more impulsive food choice patterns and demonstrate a greater likelihood of obesity than individuals who are food secure. Two specific aims are proposed: Specific aim #1: Determine the relation between food insecurity, obesity, and impulsive food choice patterns in women. The working hypothesis is that food-insecure individuals, especially those that are obese, will exhibit more impulsive food choice patterns than food-secure individuals. Specific aim #2: Determine the efficacy of an extended mindfulness-based eating strategy on impulsive choice patterns among food insecure women. The working hypothesis is that mindful eating will reduce impulsive food choice patterns relative to baseline and control conditions, and will persist to follow-up. The investigators expect mindful eating to reduce impulsive choice compared to control conditions, despite food security status.

NCT ID: NCT01982422 Completed - Anxiety Clinical Trials

Developmental Origins of Attention Deficit Hyperactivity Disorder

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

This is a study evaluating the relationship between prenatal nutrition and neural development in infants born to mothers with Attention Deficit Hyperactivity Disorder (ADHD). We are hypothesizing that women randomized to a whole food, nutrient-dense diet during their 3rd trimester of pregnancy will have infants with more advanced neural development as compared to infants born to mothers receiving standard-of-care treatment.

NCT ID: NCT01978431 Completed - Cocaine Dependence Clinical Trials

Impulsivity and Stimulant Administration

Start date: November 2012
Phase: Phase 1
Study type: Interventional

Examine the interaction between stimulants, such as cocaine and methylphenidate, and impulsivity.

NCT ID: NCT01976156 Completed - Impulsivity Clinical Trials

The Gut-brain Axis: a Novel Target for Treating Behavioral Alterations in Obesity

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

The aims of this project are to determine if dietary supplementation with NOPE-EGCG (PhosphoLeantm, 30mg NOPE+20mg EGCG per capsule) can: - rescue striatal function, - increase adherence to a diet, - reduce weight-gain after a diet, - improve performance on impulsivity, go/no-go tasks, and negative outcome learning, and - shift fat and sweet preference in overweight/obese human subjects Secondary hypotheses: Baseline brain; perceptual and cognitive measures will be associated with diet, insulin sensitivity and may vary with genotype (TaqA1 1A polymorphism).

NCT ID: NCT01902069 Completed - Alcohol Consumption Clinical Trials

The Gut-brain Axis in Food Reward and Alcohol Consumption

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

The aims of this project are to: 1. Determine if 3-weeks dietary supplementation with NOPE-EGCG (PhosphoLEANtm, 85mg NOPE+50mg EGCG per capsule) versus a placebo will improve performance on impulsivity, go/no-go tasks and negative outcome learning in heavy drinkers. 2. Evaluate whether supplementation with NOPE-EGCG versus placebo results in reductions in alcohol consumption. 3. Preliminary data in the rodent model suggests that rats treated with OEA shift preference for lower fat test stimuli. In aim 3 we will Determine if 3-weeks of supplementation with PhosphoLEAN shifts fat preference towards lower fat test puddings.

NCT ID: NCT01770600 Withdrawn - Depression Clinical Trials

Impulsivity and Thought Process Disorder in Patients With Active Suicidal Ideation and Depression

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

This study is dedicated to achieving a better understanding of how the brain processes information. Specifically, the investigators are studying cognitive function, thought process, and impulsivity in people with and without suicidal thoughts. You are being asked to participate in a research study to learn how the use of a medication, risperidone, improves your symptoms of depression. Specifically the investigators are studying the effectiveness of reducing the thought of suicide and other symptoms of severe depression. Risperidone is approved by FDA for the treatment of schizophrenia and bipolar mania, and clinical practice suggests that it might benefit patients with major depressive disorder. During clinical trials with 2607 patients, risperidone was proved to be safe. This is a pilot study to test a new indication of risperidone for treatment of severe depression. The study medication will be given in addition to usual psychiatric care.

NCT ID: NCT01314378 Active, not recruiting - Nicotine Dependence Clinical Trials

Effects of Intensive Behavioral Training Program on Impulsivity and Inhibitory Control in Smokers

IBTP
Start date: January 2011
Phase: N/A
Study type: Interventional

Dependence on tobacco derived nicotine is a major public health problem. Substance users who complete training in mindfulness subjectively report increased patience and improved motor control over their impulses. Yet, no studies have tested this perceived benefit with behavioral measures of impulse control. The investigators are conducting a randomized controlled clinical trial, which compares Cognitive-Behavioral Therapy and Mindfulness Training for tobacco smokers, using behavioral measures to investigate the effects of mindfulness training on impulsivity and inhibitory control.