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Cognition clinical trials

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NCT ID: NCT02591316 Completed - Breast Cancer Clinical Trials

Nutrition, Physical Activity, and Cognition in Breast Cancer Survivors

Start date: February 2015
Phase: N/A
Study type: Observational

The purpose of this study is to examine the relationship between nutrition, physical activity and brain function in breast cancer survivors.

NCT ID: NCT02516956 Completed - Eating Behavior Clinical Trials

Impact of Different Breakfast Meals on Food Choices, Eating Behaviors and Brain Activation

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

This project aims to demonstrate that the best breakfast meal is the one able to improve the best postprandial hunger, satiety and adiposity regulators profile as well as the best reward-related gratification, due to hedonistic parameters. To do this, 4 different breakfasts will be tested and blood tests, food choices, and attentional components will be analysed.

NCT ID: NCT02462642 Completed - Anxiety Clinical Trials

Effect of Bacopa Monniera Extract on Cognition and Anxiety and Exploration of PK Properties

Yaaddasht
Start date: March 2010
Phase: N/A
Study type: Interventional

The Indian Ayurvedic herb Brahmi (Bacopa monniera) has been used to improve cognitive functions in Indian sub-continent for many years and previous intervention studies have shown positive effects of Brahmi on cognitive performance in adults. However, the studies are conducted on various fractions and extracts and there is high likelihood of variability of composition amongst the fractions/extracts tested in these studies. Furthermore, although the findings of the previous studies overlap to some extent, they are not consistent and there is a need to replicate these findings. Further, even though Brahmi has been studied for its chemical composition and its therapeutic benefits as a whole, there are still severe gaps with respect to the complete composition of the Brahmi plant or its extracts. No published data exist on the Pharmacokinetics (PK) properties of Brahmi components. Hitherto, the evidence and the mechanistic details are still speculative and the biological activity is still phenomenological. Because of this severe knowledge gap, this study will try to repeat the findings on cognitive performance and at the same time also explore the plasma levels of its components in order to initiate the understanding of ADME aspects and its linkages to the biological effect.

NCT ID: NCT02416245 Completed - Cognition Clinical Trials

Impact of Beverage Powder With Micronutrients and Brahmi Extract on Cognitive Variables in Indian School Children

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

The aim of the current study is to investigate the beneficial impact of 4 month consumption of a beverage powder fortified with Brahmi (Bacopa monnieri) extract and multiple vitamins and minerals on short term memory as assessed using standardised cognitive test battery.

NCT ID: NCT02412410 Completed - Fatigue Clinical Trials

Optimizing Sleep/Wake Related Cognitive Efficacy

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

This is a pilot study designed to elucidate sleep/wake patterns and associated cognitive efficacy of laborists involved in shift work at Mayo Clinic Rochester.

NCT ID: NCT02386852 Completed - Blood Pressure Clinical Trials

Ginseng and Ginkgo Biloba Effects on Cognition as Modulated by Cardiovascular Reactivity

Start date: March 2014
Phase: Phase 0
Study type: Interventional

There is some evidence to suggest that ginseng and Ginkgo biloba can improve cognitive performance, however, very little is known about the mechanisms associated with such improvement. Here, we tested whether cardiovascular reactivity to a task is associated with cognitive improvement.

NCT ID: NCT02360917 Completed - Cancer Clinical Trials

Emerging From the Haze™- Measuring the Impact of a Psycho-education Program on Perceived Cognition After Breast Cancer Treatment

Haze
Start date: July 6, 2015
Phase: N/A
Study type: Interventional

At Cedars-Sinai Medical Center, we have developed a novel curriculum for a 6-week psycho-educationally-based, cognitive behavioral program to help patients with subjective cognitive complaints after cancer treatment, titled Emerging from the Haze™ (Haze). Each series meets once a week for 2 hours for 6 weeks. The leading neuropsychologist covers material such as guided relaxation, behavioral strategies for automatic/negative thoughts, compensatory strategies for attention and memory, executive functioning, pacing, and balance. Each Haze series will be electronically delivered in a live format to our satellite site, The University of Kansas.

NCT ID: NCT02212366 Completed - Depression Clinical Trials

To Enhance Cognition in Late Life Depression Using Transcranial Direct Current Stimulation

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

Late Life Depression (LLD) is a serious health problem which not only causes depressed mood but also results in impairments in memory and attention. These impairments are likely to be resistant to treatment, which increases the chances of developing dementia even after successful treatment of mood.This study is a randomized controlled trial of transcranial Direct Current Stimulation (tDCS) in people with LLD to enhance their cognition after successful treatment of mood with established medications. tDCS is non invasive, relatively inexpensive and portable, and has been found to be safe.This study also serves as a pilot study to assess the effects of tDCS on cognition and neurophysiologic markers of cognition among patients with LLD. Primary study hypothesis is that participants Participants randomized to tDCS will perform better on a working memory task 2 weeks and 3 months following the tDCS course.

NCT ID: NCT02177942 Completed - Cognition Clinical Trials

A Clinical Trial to Study the Impact of a Nutritional Beverage on Tests of Memory in Healthy Preschool Age Children

Start date: June 20, 2014
Phase: N/A
Study type: Interventional

The effect of supplementation using both protein and multiple micronutrients in preschool age children on cognitive performance and growth is unknown. The study will compare the effect of combination of protein and multiple micronutrients on indicators of cognitive performance and growth in preschool age children. Cognitive performance and anthropometric assessments will be measured at baseline and at 6 months.

NCT ID: NCT02128919 Completed - Schizophrenia Clinical Trials

Transcranial Direct Current Stimulation (tDCS) As A Treatment For Cigarette Craving and Cognitive Deficits in Schizophrenic

TDCSSCHIZ
Start date: April 2012
Phase: N/A
Study type: Interventional

This is a study of the effects of tDCS on smoking, craving for cigarettes, cognition, and psychiatric symptoms in schizophrenic patients who are current smokers or have a history of regular cigarette smoking. It assesses smoking with CO monitoring, nicotine and nicotine levels, and craving with QSU scale and response to craving slides. Cognition is measured by MCCB, symptoms are measured by PANSS and hallucination scale. This is a double-blind sham-controlled study with active tDCS 2ma or 20 minutes over 5 days, and sham tDCS for 40 seconds on each sham occasion.