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Cognition Disorders clinical trials

View clinical trials related to Cognition Disorders.

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NCT ID: NCT03290599 Completed - Clinical trials for Post Operative Cognitive Dysfunction

Effect of Preoperative Hospitalization Duration on Post-operative Cognitive Dysfunction

Start date: November 1, 2013
Phase: N/A
Study type: Observational

Post-operative cognitive dysfunction is defined as a decrease in cognitive functions which develop following surgery and anesthesia administration that can last up to weeks or even months after surgery. In this study, our main objective was to investigate the effect of preoperative hospitalisation period on early post operative cognitive dysfunction development and its risk factors in patients who underwent total hip replacement surgery for hip fractures under regional anesthesia.

NCT ID: NCT03286439 Completed - Cognitive Deficit Clinical Trials

Recovery After Medical or Surgical Treatment

Start date: November 13, 2017
Phase:
Study type: Observational

This study aims to investigate the in-hospital care as well as the cognitive status, quality of life, physical function and risk of anxiety and depression, sleep disorders and drug use in a Danish cohort of both medical and surgical patients with acute critical illness without admittance to ICU (Intensive Care Unit) treatment, at three and twelve months after hospital discharge.

NCT ID: NCT03279835 Completed - HIV-1 Clinical Trials

Evaluation of a Short Version Computerized Test for Processing Speed to Detect Cognitive Disorders in HIV+ Patients

NEURACog
Start date: March 16, 2017
Phase:
Study type: Observational

The objective of this prospective study is to evaluate the prevalence of neurocognitive impairments in HIV infected patients comparing patients with and without HAART. Recent studies have demonstrated a specific HIV infected patients neurocognitive disorders profile. These cognitive disorders concern primarily information processing speed, memory recall, attentional abilities, work related memory, executive functions, and psychometrical speed. This cognitive profile is similar to another highly documented one, described for another central nervous system disease (CNS): multiple sclerosis. In both CNS diseases, the earliest and most severe disorder is the one related to the information processing speed. For the multiple sclerosis patients, a short cognitive test (SDMT) is actually used not only to identify cognitive disorders presence, but also in order to predict a long term disability worsening. A digital version of this test (CSCT), has recently been developed in order to make this early evaluation easier. We hypothesize that CSCT alteration would also predict HAND, in HIV infected patients. A complete neuropsychological assessment is highly time and personal consuming. This short (approximatively 2 minutes) digital test would be highly helpful to identify patients, who will need a more extensive neuropsychological assessment.

NCT ID: NCT03275363 Recruiting - Clinical trials for Mild Cognitive Impairment

The University of Hong Kong Neurocognitive Disorder Cohort

Start date: September 1, 2014
Phase: N/A
Study type: Observational [Patient Registry]

The HKU Neurocognitive Disorder (NCD) Cohort is a hospital-based, prospective, observational study of older HK Chinese adults with cognitive impairment, with a special focus on studying patients with subjective cognitive decline and mild cognitive impairment.

NCT ID: NCT03273439 Completed - Schizophrenia Clinical Trials

A Study of rTMS for Cognitive Deficits in Chronic Patients With Schizophrenia

Start date: July 1, 2012
Phase: N/A
Study type: Interventional

In this study, we assessed the therapeutic effects and safety of left dorsolateral prefrontal cortex (DLPFC) high-frequency repetitive transcranial magnetic stimulation (rTMS) on negative symptoms of schizophrenia. We evaluated the efficacy of rTMS on cognition in patients with chronic schizophrenia.

NCT ID: NCT03252054 Completed - Dementia Clinical Trials

Memory and Attention Disorders and Malnutrition in Hospital Setting

Start date: September 1, 2016
Phase:
Study type: Observational

This is a cross-sectional observational study that investigates the prevalence of memory disorders, attention disorders (suggesting delirium), and malnutrition in hospitalized older adults (aged 70 years or over) in a tertiary care centre, using rapid screening toos (Six-item screener for memory disorders, Months of the Year Backwards Test for delirium, and NRS-2002 and Mini Nutritional Assessment Short Form for malnutrition).

NCT ID: NCT03246269 Completed - Dementia Clinical Trials

Normative Values for the German Version of the Montreal Cognitive Assessment (MoCA)

MoCA-Norm
Start date: December 2016
Phase:
Study type: Observational

This observational cohort study in healthy volunteers establishes normative data for the German version of the Montreal Cognitive Assessment (MoCA) and investigates the possible impacts of demographics on the MoCA total score.

NCT ID: NCT03242395 Completed - Depression Clinical Trials

PRIME: Cognitive Outcome Following Major Burns

PRIME
Start date: October 2014
Phase: N/A
Study type: Observational

PRIME aims to demonstrate through neurocognitive assessment that BICU patients will have a degree of neurocognitive dysfunction following a major burn, that this neurocognitive dysfunction is due to an underlying neuroinflammatory process by fMRI neuroimaging techniques, and that the neurocognitive deficit is associated with a reduced quality of life.

NCT ID: NCT03221452 Active, not recruiting - Clinical trials for Diabetes Mellitus, Type 2

Adaptation of a Cognitive Training Intervention for Diabetes Self-Management

Start date: September 2, 2016
Phase: N/A
Study type: Interventional

The aims of this project are: (1) to refine an existing cognitive rehabilitation intervention and tailor it for persons with T2DM by using current literature and interview data from 10 participants with T2DM and (2) to conduct a feasibility study of the adapted intervention with 20 participants with T2DM. The intervention consists of 8 weekly group educational sessions to teach compensatory cognitive strategies. Participants will also use a web-based, game-like program to build on the didactic information and practice activities to improve cognitive health.

NCT ID: NCT03205709 Active, not recruiting - Clinical trials for Mild Cognitive Impairment

Cognitive Training and Neuroplasticity in Mild Cognitive Impairment

CogTraining
Start date: November 29, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate if systematic cognitive training can improve cognitive performance in participants (55 and older) with memory loss. This study will evaluate the effects of Computerized Cognitive Training (CCT) for improvement in everyday cognitive and function status, in addition to long-term changes in brain networks over an 18-month period. Although there is no distribution of medication for this study, participants are required to have an at-home computer.