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Cognitive Impairment clinical trials

View clinical trials related to Cognitive Impairment.

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NCT ID: NCT02462291 Completed - Alzheimer Disease Clinical Trials

New Approach for Treatment of Behavioral Disorders in Alzheimer's Disease (Alzheimer's Behavioral and Cognitive Disorders)

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

Alzheimer's disease (AD) is the most frequent form of dementia, causing high level of disability with elevated social costs. Alternative solutions to the standard pharmacological therapies have been studied in order to reduce the use of medications that frequently generates side effects and worsen patients' quality of life. A recent alternative treatment for AD is the Environmental Ecological Therapy (EET) that, with the use of therapeutic gardens, seems to reduce behavioral disorders (BD). However, the effectiveness of this approach is still mater of debate. Therefore, the aim of this trial will be to analyze the effects of EET, in people with severe AD.

NCT ID: NCT02415517 Completed - Clinical trials for Cognitive Impairment

Cognitive Training in Heart Failure Study (CogTrain-HF)

CogTrain-HF
Start date: January 2014
Phase: N/A
Study type: Interventional

The daily routine in clinical settings often showed cognitive impairments in patients with congestive heart failure, particularly in terms of executive functions, episodic memory, perceptual speed and attention. It is assumed that cognitive impairments in patients with congestive heart failure may lead to deficits in medication-adherence and self-care abilities, resulting in increased healthcare costs. Recent studies reported performance improvements after cognitive training that transferred to new, untrained tasks and abilities in healthy subjects across a wide range of ages. This study investigates the effects of cognitive training in patients with congestive heart failure.

NCT ID: NCT02409446 Completed - Inflammation Clinical Trials

Metabolic, Vascular and Cognitive Effects of Treatment With Anthocyanins

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

The purpose of this study is to examine weather treatment with anthocyanins will affect lipid profile, markers of inflammation and oxidative stress in addition to antioxidative level in serum to the better in persons with increased risk of dementia. The purpose of this study is to examine weather treatment with anthocyanins will increase the score of relevant tests of cognitive function. The investigators will do an open pilot study where patients receive anthocyanin for 16 weeks. 34 patients are expected to be included. In addition we will include 20 healthy Controls.

NCT ID: NCT02363114 Active, not recruiting - Stroke Clinical Trials

DOC Utility: Screening of Depression, Obstructive Sleep Apnea and Cognitive Impairment

Start date: April 1, 2014
Phase:
Study type: Observational [Patient Registry]

The primary objective of this study is to determine whether baseline DOC screening can add to clinical and demographic data to predict the occurrence of a composite negative outcome (any of: recurrent stroke, myocardial infarction, death, or admission to a long-term care (LTC) / complex continuing care (CCC) facility) within one year of screening, in stroke prevention clinic patients.

NCT ID: NCT02360215 Completed - Clinical trials for Cognitive Impairment

Memantine Hydrochloride and Whole-Brain Radiotherapy With or Without Hippocampal Avoidance in Reducing Neurocognitive Decline in Patients With Brain Metastases

Start date: July 2015
Phase: Phase 3
Study type: Interventional

This randomized phase III trial compares memantine hydrochloride and whole-brain radiotherapy with or without hippocampal avoidance in reducing neurocognitive decline in patients with cancer that has spread from the primary site (place where it started) to the brain. Whole brain radiotherapy (WBRT) is the most common treatment for brain metastasis. Unfortunately, the majority of patients with brain metastases experience cognitive (such as learning and memory) deterioration after WBRT. Memantine hydrochloride may enhance cognitive function by binding to and inhibiting channels of receptors located in the central nervous system. Radiation therapy uses high energy x-rays to kill tumor cells and shrink tumors. Using radiation techniques, such as intensity modulated radiotherapy to avoid the hippocampal region during WBRT, may reduce the radiation dose to the hippocampus and help limit the radiation-induced cognitive decline. It is not yet known whether giving memantine hydrochloride and WBRT with or without hippocampal avoidance works better in reducing neurocognitive decline in patients with brain metastases.

NCT ID: NCT02343029 Completed - Dementia Clinical Trials

Physical Activity and Cerebral Metabolism in the Elderly: a Randomised Controlled Trial

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

Physical activity exerts a variety of long-term health benefits in older adults.This randomised controlled trial investigates the effect of a 12-week physical exercise program on the change in cerebral metabolism as assessed with Magnetic Resonance Spectroscopic Imaging. Follow-up lasts for 6 months.

NCT ID: NCT02315807 Recruiting - Stroke Clinical Trials

Neurostimulation for Cognitive Rehabilitation in Stroke

NeuroCog
Start date: December 2015
Phase: Phase 2/Phase 3
Study type: Interventional

Transcranial direct current stimulation has shown promising results in stroke patients. This study is a double blind, sham-controlled clinical trial aiming to compare the long-term effects of stimulation in two different cognitive regions after a stroke. Sixty patients who suffer from chronic strokes will be randomized into 1 of 3 groups: dorsolateral prefrontal cortex, cingulo-opercular network and motor primary cortex (control). Each group will receive transcranial direct current stimulation for 20 minutes for 10 consecutive working days (2 weeks). Patients will be assessed with a Dysexecutive Questionnaire, Semantic Fluency test, categorical verbal fluency and Go-no go tests, Wechsler Adult Intelligence Scale, Rey Auditory-Verbal Learning Test, Letter Comparison and Pattern Comparison Tasks at baseline, after their tenth stimulation session (week 2) and endpoint (week 4). Those who achieve clinical improvement with neurostimulation will be invited to receive treatment for 12 months as part of a follow-up study.

NCT ID: NCT02310217 Completed - Hypertension Clinical Trials

Validation of New Tools for the Assessment of Cognitive Functions and Connectivity Network in Hypertensive Patients

Start date: February 2015
Phase:
Study type: Observational

The relationship among hypertension, aging and cognitive decline is complex and not completely understood. Purpose of this project will be evaluating early markers of cognitive deterioration in patients with arterial hypertension. In particular, this cross-sectional observational study will be articulated in three phases: 1. Neuropsychological evaluation of general cognitive abilities 2. Identification and measurement of specific biomarker levels 3. Correlation among hypertension, cognitive abilities and biomarkers.

NCT ID: NCT02305836 Recruiting - Clinical trials for Cognitive Impairment

Effect of Electroacupuncture Combined With Donepezil for Treating Alzheimer's Disease

Start date: June 2017
Phase: Phase 2
Study type: Interventional

A prospective randomized controlled trial aimed at assessing if electroacupuncture (EA) combined with donepezil is more effective than donepezil for improving the cognitive function of AD patients. The hypothesis of this study is as follow: - Is the short-term effect of EA combined with donepezil better than donepezil on improving cognitive function of patients with Alzheimer's disease after 12 weeks' treatment? - Whether the effect of EA combined with donepezil on improving cognitive function can last until the end of 6 months' follow-up?

NCT ID: NCT02301676 Not yet recruiting - Clinical trials for Cognitive Impairment

Long Term Postoperative Cognitive Dysfunction in the Elderly Patients

Start date: December 2014
Phase: Phase 4
Study type: Interventional

The purposes of this study are to determine whether long-term postoperative cognitive dysfunction (POCD) is occured after general anesthesia and anesthetic drugs have an effect on the result about POCD.