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Cognitive Ability, General clinical trials

View clinical trials related to Cognitive Ability, General.

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NCT ID: NCT03137836 Completed - Sedentary Lifestyle Clinical Trials

Classroom Standing Desks for Reducing Sitting Time in Children

Start date: January 4, 2016
Phase: N/A
Study type: Interventional

In this trial the investigators aim to verify the potential impacts of a multi-level intervention with standing desks on behavior and cognitive function in children

NCT ID: NCT02881788 Active, not recruiting - Clinical trials for Cognitive Ability, General

Minnesota Healthy Brain Initiative

Start date: August 2016
Study type: Observational [Patient Registry]

Minnesota Healthy Brain Initiative will be an ongoing project that aims to increase awareness regarding brain health and its maintenance as well as increasing awareness of the impact of alcohol on brain function. In the immediate future, we hope to obtain data from a non-injured normative, diverse population represented by the state fair patrons.

NCT ID: NCT02853279 Completed - Obesity Clinical Trials

Physical Activity and Intermittent Exercise Training for Cardiovascular and Cognitive Gain in Obese Women

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

One hundred participants from a combination of (a) local advertisements and/or (b) those whose details are held on a research database (of previous volunteers indicating willingness to be contacted about future studies) will be sought to volunteer for this study. Written informed consent will be gained following greater than 48 hours for the purpose of reading the Participant Information sheets. The study will then involve two stages (i) recruiting participants for a cross sectional analysis of the relationship between physical activity levels and cardiovascular and cognitive function, and (ii) a longer exercise training study in a subsample of these volunteers (i.e. participants who volunteer to exercise train). Participants for stage 1 will then visit the laboratory in the University on three occasions (over a three week period) to be assessed for body composition, exercise tolerance, current physical activity levels, cognitive function and arterial and cardiac health. Each visit will last for 60 - 90 minutes. Participants will then be provided with an accelerometer to wear for a period of one week in order to assess movement counts and sedentary behaviour. Stage 2 will include only those participants who have volunteered for the exercise training component (approx 60). These participants will then be randomly divided into two groups. Both groups will exercise three times per week for 12 weeks duration. Group 1 will exercise in a traditional manner at a moderate intensity, whilst the second group will exercise at a heavy intensity but in short bursts. Both groups will complete the same amount of work but in two differing modes. Both groups will attend the laboratory twice per week for supervised exercise sessions and also perform one home based 30 minute brisk walk per week. All participants will be re-examined at 12 weeks.

NCT ID: NCT02843282 Active, not recruiting - Bipolar Disorder Clinical Trials

Reasoning Training in Individuals With Bipolar Disorder

Start date: April 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to examine cognitive and brain changes in individuals with bipolar disorder as a result of a cognitive training intervention.

NCT ID: NCT02820805 Completed - Clinical trials for Cognitive Ability, General

Dietary Carbohydrate Consumption on Memory Performance and Mood in Children

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

The purpose of this study is to determine the effect of carbohydrates on blood glucose levels, subjective appetite, mood, and memory performance in 9 to 14 year old normal weight (NW) and overweight or obese (OW/OB) children.

NCT ID: NCT02780739 Completed - Clinical trials for Cognitive Ability, General

INSIGHT, A Comprehensive, Multidisciplinary Brain Training System

Start date: March 2014
Phase: N/A
Study type: Interventional

Adaptive reasoning and problem-solving are critical skills that allow for accurate decisions to be made based on varying levels of information. In many situations these decisions must be made and communicated under stressful, time-sensitive conditions. In such contexts, an ability to apply inductive and deductive reasoning to complex, ambiguous, and/or novel problems is critical. The objective of the INSIGHT project is to establish a comprehensive and rigorous brain training protocol to significantly improve adaptive reasoning and problem solving. We will examine a variety of interventions (cognitive training, physical fitness training, physiological stimulation, , and combinations thereof) to assess their ability to improve adaptive reasoning and problem solving abilities. Multimodal interventions are hypothesized to act synergistically to significantly enhance fluid intelligence (Gf) and underlying brain structure and function.

NCT ID: NCT02726906 Recruiting - Aging Clinical Trials

Lifestyle Enriching Activities for Research in Neuroscience Intervention Trial: LEARNit Study

Start date: July 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to examine the effects of modifiable lifestyle factors including exercise and healthy living on brain health. The investigators will compare 2 types of interventions, moderate aerobic walking vs. healthy living education, over 6 months to evaluate changes in brain health, cognition, and physical function in older adults with cognitive concerns.

NCT ID: NCT02630667 Completed - Clinical trials for Dietary Modification

The Acute Effects Fortified Nutritional Supplementation on Childhood Cognition

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

The aim of this study is to investigate the acute effects of ingestion of carbohydrates - with different glycemic profiles - on cognitive function among preadolescent children (i.e., 9-10 years).

NCT ID: NCT02567227 Recruiting - Motor Activity Clinical Trials

Cognitive Remediation to Improve Mobility in Sedentary Seniors

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

The investigators propose to conduct a single-blind randomized clinical trial to test the efficacy of a computerized cognitive remediation intervention program on improving locomotion in sedentary seniors, a group at an especially high risk for disability. The hypothesis is that executive functions will respond to the cognitive remediation program and in turn enhance locomotion.

NCT ID: NCT02461693 Completed - Clinical trials for Cognitive Ability, General

Evaluating the Role of Expectations in Response to Caffeine Consumption: An RCT

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

The purpose of this project is to examine the effect of expectancy on mood and alertness after consumption of caffeine "treatment" or placebo "control" pill, given that participants know their probability for receiving the caffeine versus placebo pill. Participants will be randomly assigned a probability (ranging from 0-100%) of receiving caffeine vs. placebo, and this probability will be revealed to them before consumption of the assigned pill and subsequent cognitive testing. At the time of consumption, neither study staff administering the intervention nor participants will know for certain which pill is given to each participant. Pill assignment will depend on pre-determined randomization probabilities, which will be provided and assigned by the study statistician. By revealing participants' individual probability of receiving the caffeine pill, we will induce positive or negative expectancies regarding likelihood for receipt of the caffeine pill. These experimental manipulations will: 1) estimate the effect of expectancy on cognitive and affective outcomes, and 2) allow for a more direct estimate of the effect of the caffeine pill under real-world conditions than would a conventional randomized trial.