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Attention clinical trials

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NCT ID: NCT01518738 Completed - Attention Clinical Trials

Attention Training

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

The purpose of this study is to understand whether attention training is effective in moderating mind wandering.

NCT ID: NCT01427231 Completed - Mental Health Clinical Trials

Short-term Effect of Glucose and Sacharose Ingestion on Cognitive Performance and Mood in Elderly

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

The objective of the current study is to determine the acute effect of a glucose drink and a sacharose drink compared to a placebo on cognitive performance in elderly with light memory complaints. The investigators expect that the sugar containing drinks will improve memory and attentional functions. Furthermore, blood glucose response will be measured.

NCT ID: NCT01365897 Completed - Executive Function Clinical Trials

Effectiveness of Modafinil in Improving Cognitive Performance of University Students

Start date: September 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether modafinil is effective in the improvement of mnesic performance and executive functions of university students from high academic performance.

NCT ID: NCT01143194 Completed - Memory Clinical Trials

A Randomized, Placebo-Controlled, Double-Blind, Crossover Study to Evaluate the Effects of Three Doses of the Dietary Supplement oréVida™ on Alertness, Attention and Concentration in Healthy Men and Women

Start date: March 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate the effects of the dietary supplement oréVida™ (active ingredient on the basis of a culinary herb)administered twice daily in an acute study on an improvement in vigilance, attention, concentration, memory and mood in 45 healthy men and pre-menopausal women, aged 35-50 years, inclusive. oréVida™ is considered a dietary supplement, and therefore it is not an approved drug by the Food and Drug Administration (FDA). It is regulated like a food. The U.S. Food and Drug Administration does not strictly regulate herbs and dietary supplements. We do not claim that this supplement is meant to treat any ailment.

NCT ID: NCT01124721 Completed - ADHD Clinical Trials

Effects of Cognitive Training on Academic Task Performance in Attention Deficit Hyperactivity Disorder (ADHD)

Cog-RAST
Start date: January 2008
Phase: N/A
Study type: Interventional

Impaired WM is a central deficit in ADHD. A computerized training program, Cogmed, has been shown to increase WM capacity in children with ADHD. It is not known whether the training improves behavior associated with classroom learning, such as remaining on-task and inhibiting off- task behavior. The aim of this study is to utilize ecologically valid measures to investigate training's effect on observable ADHD behavior in conjunction with more standard measures. Subjects will be randomly assigned to a Cogmed versus an active "placebo" condition in which the tasks do not increase in difficulty level in a double-blinded fashion. The effects of the active Cogmed versus placebo computer training will be compared on measures in children with ADHD.

NCT ID: NCT01075958 Completed - Mood Clinical Trials

Polyunsaturated Fatty Acids (PUFA) Status and Cognitive Function in Healthy Young Adults

Start date: July 2007
Phase: N/A
Study type: Observational

To date, the relationship between omega-3 polyunsaturated fatty acids (n-3 PUFAs) in cognitively intact individuals has only been examined in a limited number of studies; it is at present unknown whether supplementation with n-3 PUFAs can improve cognitive function and mood in this population. Further to this, it still remains to be established whether a relationship exists between peripheral fatty acid status—reflective of dietary n-3 PUFA intake—and cognitive function in this population. The current study therefore aims to address this issue by exploring the relationship between serum PUFAs and specific cognitive functions in a sample of healthy adults. To this end, participants will complete a range of cognitive tasks evaluating performance across the domains of attention, memory and executive function. Self-report mood assessments will be included as secondary measures.

NCT ID: NCT00988702 Active, not recruiting - Clinical trials for Electroencephalography

Shaolin Dan Tian Breathing Fosters Relaxed and Attentive Mind

Start date: October 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The present study aimed to utilize these well-known neuroelectrophysiological techniques to investigate the relatively less studied Shaolin Dan Tian Breathing (DTB) technique.

NCT ID: NCT00662142 Completed - Healthy Clinical Trials

Effect of 8-Week Dietary DHA Supplementation on Cerebral Blood Flow and Metabolic Function

Start date: January 2006
Phase: Phase 3
Study type: Interventional

The goal of this study is to determine if 8-week dietary treatment with the omega-3 fatty acid docosahexaenoic acid (DHA) improves attention performance and associated cortical activity and metabolism in 8 - 10 year old males that were not breast-fed during infancy.

NCT ID: NCT00527969 Completed - Cognition Clinical Trials

Cognitive, Emotional, Physical and Psychosocial Effects of Panax Quinquefolius L

REMEMBER-fX
Start date: July 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the efficacy and safety of REMEMBER-fX (HT1001, an extract of Panax quinquefolius) in a human sample using standard clinical neuropsychological instruments and side effects rating scales.