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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: NCT02575365 Terminated - Cognition Clinical Trials

Effect of Fingolimod on Neurodegeneration

Start date: February 16, 2016
Phase: Phase 4
Study type: Interventional

This was a 24-month, open-label, multicenter study with a single treatment arm design. Primary objective of this study was: -To investigate the effects of Fingolimod on cognitive performance in highly active relapsing remitting multiple sclerosis patients Secondary objectives of this study were: - To investigate the correlation between the effect of fingolimod on cognitive performances and MRI data. - To evaluate the effect of fingolimod on biomarkers (24 hydroxy cholesterol, osteopontin and matrix metalloproteinases) related to neurodegeneration - To investigate the effect of fingolimod on brain gray matter atrophy and thalamic atrophy. Polulation The hope was to recruit a minimum of 80 relapsing remitting MS (RRMS) patients according to the McDonald criteria.

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: NCT02246075 Withdrawn - Dementia Clinical Trials

Study of the Safety of Two Doses of Investigational Study Drug EVP-6124 in Subjects With Alzheimer's Disease Currently Receiving Memantine

Start date: July 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety of 2 fixed doses of EVP-6124 hydrochloride (HCl) compared to placebo for 24 weeks in subjects with mild to moderate Alzheimer's disease who are concurrently receiving stable treatment with memantine and currently receiving stable treatment or previously treated with an acetylcholinesterase inhibitor.

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.