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Cognition Disorders clinical trials

View clinical trials related to Cognition Disorders.

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NCT ID: NCT02054507 Completed - Clinical trials for Complications of Prematurity

Prematurity Related Risks of Cognitive Impairment at School Age

NEORIS
Start date: April 2013
Phase: N/A
Study type: Interventional

The main purpose of this study is to better evaluate prematurely born children cognitive development at school age, with regards to birth conditions but also to social situation, intra family relationships, and modalities of care. The study will be divided into 3 parts: 1. Children born prematurely in our level III referral Center will undergo psychometric evaluation at 8 to 11 years of age by routine cognitive test. The relationships between cognitive scores and neonatal characteristics will be determined and compared to the results of schoolmates born at term. 2. The quality of parent and child relationship will be evaluated by a standardized questionnaire allowing the evaluation of persistent stress trauma related to premature birth. 3. An anthropologic study of the utilization of care resources will also be performed within the follow-up network taking care of these children.

NCT ID: NCT02051270 Completed - Clinical trials for Mild Cognitive Impairment

Cognitive Impairment and Balance in Elderly

Start date: January 2014
Phase: N/A
Study type: Observational

One important issue in older adults with cognitive problems is the higher risk of fall due to decreased motor function and balance. The objective of this study is to evaluate the repercussions of mild cognitive impairment in balance in elderly.

NCT ID: NCT02050464 Completed - Alzheimer Disease Clinical Trials

Computational Tools for Early Diagnosis of Memory Disorders

ProsKuopio
Start date: December 2013
Phase: N/A
Study type: Observational [Patient Registry]

The Virtual Physiological Human: DementiA Research Enabled by IT (VPH-DARE@IT) is a four-year IT-project funded through the European Union (EU). The project consortium involves a total of 21 universities and industrial partners from 10 European countries. The project delivers the first patient-specific predictive models for early differential diagnosis of dementia and their evolution. An integrated clinical decision support platform will be validated / tested by access to a dozen databases of international cross-sectional and longitudinal studies. As a part of the VPH-DARE@IT project, a new prospective cohort will be collected in Kuopio. This prospective cohort will be used to test further the modeling approaches and tools developed by using the retrospective databases.

NCT ID: NCT02049411 Completed - Clinical trials for Postoperative Cognitive Dysfunction

Ketamine and Changes of the Short Portable Mental Status Questionnaire

SPMSQ-E
Start date: June 2013
Phase: Phase 2
Study type: Interventional

- Cognitive changes are related to aging, affecting the performance of older patients in the solution of problems and the execution of tasks. This phenomenon has been observed as a decline of neurophysiological domains, especially memory, and the velocity of thought. - Anesthesia and surgery performed contributes to its development then, is named post-operative cognitive dysfunction (POCD). The incidence varies due to conditions of: 1. Anesthesia and surgery. 2. The time elapsed after surgery. 3. The population studied, and the type of cognitive test employed. - The aim of this study is to evaluate the changes around the Short Portable Mental Status Questionnaire (SPMSQ-E) after ketamine administration on ophthalmic surgery on the common conditions of geriatric patients, —comorbid and settings as minor surgery—.

NCT ID: NCT02035865 Completed - Cognition Disorders Clinical Trials

Mood and Cognitive Outcome After Heart Transplantation (the MOODHEART Study)

Start date: December 2013
Phase:
Study type: Observational

The investigators aim at characterizing neuropsychiatric consequences of heart transplantation (HTX) and at assessing the impact of depressive symptoms after HTX on mortality and cardiac allograft vasculopathy (CAV).

NCT ID: NCT02035436 Completed - Delirium Clinical Trials

Non-sedation Versus Sedation With a Daily Wake-up Trial in Critically Ill Patients Receiving Me-chanical Ventilation - Effects on Cognitive Function

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

Through many years, the standard care has been to use continuous sedation of critically ill patients during mechanical ventilation. However, preliminary randomised clinical trials indicate that it is beneficial to reduce the sedation level in these patients. The NONSEDA trial is an investigator-initiated, randomised, clinical, parallel-group, multinational, superiority trial designed to include 700 patients from at least six ICUs in Denmark, Norway and Sweden, comparing no sedation with sedation and a daily wake-up trial during mechanical ventilation. This is a substudy of the NONSEDA trial, concerning 250 patients included at trialsite Kolding, Denmark. The aim of the substudy is to assess the effects of no sedation on delirium during admission and cognitive function after discharge from ICU. Our hypothesis is that critically ill patients who are not sedated during mechanical ventilation will have better cognitive function after discharge.

NCT ID: NCT02023645 Active, not recruiting - Clinical trials for Mild Cognitive Impairment

The Effects of a Carotenoid Intervention on Cognitive Function

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

Past research suggests that retinal lutein levels are related to cognitive function as measured via behavioral tests. The goal of the present study is to investigate the relationship between lutein and cognitive function in a wider variety of the population (young, healthy adults and older adults), using a wider variety of methods (behavioral testing and neuroimaging).

NCT ID: NCT02008357 Completed - Cognition Disorders Clinical Trials

Clinical Trial of Solanezumab for Older Individuals Who May be at Risk for Memory Loss

A4
Start date: February 28, 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test whether an investigational drug called solanezumab can slow the progression of memory problems associated with brain amyloid (protein that forms plaques in the brains of people with Alzheimer Disease [AD]).

NCT ID: NCT02007265 Completed - Stroke Clinical Trials

Post-stroke Triage "DOC": Simple Screening for Depression, Obstructive Sleep Apnea and Cognitive Impairment

Start date: April 2012
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether simple, evidence-based clinical screening be quickly and feasibly implemented (>85% of patients in an average of <6 minutes) in large-volume urgent transient ischemic attack (TIA)/stroke clinics to identify individuals at high risk for the three most common and devastating post-stroke co-morbidities (depression, obstructive sleep apnea and cognitive disorders).

NCT ID: NCT01998711 Completed - Clinical trials for Mild Cognitive Impairment

Impact of a Memory Group for Older Adults Reporting Memory Difficulties

Start date: October 2004
Phase: N/A
Study type: Interventional

Aims: To evaluate the efficacy of a brief intensive intervention for persons with mild cognitive impairment, assisted by family members or friends. To equip persons with mild cognitive impairment with specific skills to prevent memory failures and improve the capacity of patients and families to cope with everyday memory difficulties.