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Cognition Disorders clinical trials

View clinical trials related to Cognition Disorders.

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NCT ID: NCT01219244 Completed - Clinical trials for Mild Cognitive Impairment

Effects of Dietary Interventions on the Brain in Mild Cognitive Impairment (MCI)

Start date: August 2010
Phase: Phase 2/Phase 3
Study type: Interventional

The study will investigate whether dietary modification could provide positive effects on brain functions in elderly people with mild cognitive impairment.

NCT ID: NCT01212692 Completed - Clinical trials for Mild Cognitive Impairment (MCI)

Effects of Mental Stimulation in Patients With Mild Cognitive Impairment

Start date: October 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to learn if activities that challenge the brain (mentally stimulating activities) can improve memory and other types of thinking in patients with Mild Cognitive Impairment. The study will compare the effects of different methods of mental stimulation.

NCT ID: NCT01205464 Completed - Fatigue Clinical Trials

Effects of Doxycycline on Persistent Symptoms Post-neuroborreliosis

Start date: February 2005
Phase: N/A
Study type: Interventional

The aim of this randomised, double-blind crossover study was to determine whether Doxycycline has an impact on the persistent symptoms post-neuroborreliosis, through alterations in the immune response and whether such an effect could influence the clinical outcome.

NCT ID: NCT01199913 Completed - Clinical trials for Postoperative Cognitive Dysfunction

POCD in Elderly Patients Following Desflurane or Sevoflurane General Anesthesia

Start date: August 2010
Phase: N/A
Study type: Observational

The use of desflurane in elderly subjects (>65 years old) undergoing general anesthesia with endotracheal intubation will result in decreased POCD compared to sevoflurane if the patient's MAP is within 20% of the patient's baseline and the cerebral suppression state index stays within the moderately anesthetized range during general anesthesia.

NCT ID: NCT01195961 Withdrawn - Cognition Disorder Clinical Trials

Facilitating Numerical Processing With Transcranial Stimulation in Developmental Dyscalculia

Start date: August 17, 2010
Phase: N/A
Study type: Observational

Background: - Developmental dyscalculia is a learning disability in which individuals have difficulty learning or comprehending mathematics or other number concepts (such as keeping score during games, measuring time, or estimating distance). Developmental dyscalculia affects certain parts of the brain that are required for processing numbers. Research has shown that a form of brain stimulation called transcranial direct current stimulation (tDCS), applied when healthy individuals are being trained to carry out tasks with numbers, improved the ability to process numbers and solve math problems. More research is needed about whether tDCS can improve number processing in people with developmental dyscalculia. Objectives: - To examine whether the effects of transcranial direct current stimulation can help individuals with developmental dyscalculia perform mathematical calculations. Eligibility: - Individuals between 18 and 50 years of age who have been diagnosed with developmental dyscalculia, or are healthy volunteers without dyscalculia. Design: - Participants will have a screening visit and seven study visits. The screening visit and six of the study visits will take place consecutively over the course of 6 days, and the final visit will take place 3 months after the initial participation. - Participants will be screened with a medical history, physical and neurological examination, and a brief examination to test for dyscalculia and determine the participant's dominant hand. - Participants will be randomly assigned to one of two groups for the study. One group will receive tDCS during training to perform a task with numbers, and the other group will receive the same training with sham stimulation. Participants will not know which group they are in. - During the study visits, participants will be trained on number tasks on 6 consecutive days. Before the tDCS or sham stimulation is applied at the beginning of the experiment and at the end of each training day, participants will perform other tasks with numbers. Participants will be evaluated based on the accuracy and speed with which they respond to the questions. - At the followup visit, participants will perform the same number tasks they completed during the study visits. No tDCS will be performed at this visit.

NCT ID: NCT01186471 Completed - Schizophrenia Clinical Trials

The Effect of Nicotine on Arousal, Cognition and Social Cognition in Schizophrenic Patients

Start date: May 2010
Phase: Phase 0
Study type: Interventional

This study in patients with stable schizophrenia will investigate the effect of nicotine on arousal, cognitive task and social cognition after acute dose administration.

NCT ID: NCT01186289 Withdrawn - Clinical trials for Neurocognitive Dysfunction

Statin Therapy To Limit Cognitive Dysfunction After Cardiac Surgery

Start date: October 2010
Phase: N/A
Study type: Interventional

The primary aim of our prospective, randomized, double-blind interventional clinical trial is to determine the effectiveness of high dose atorvastatin therapy to reduce post operative cognitive dysfunction (POCD) in patients undergoing cardiac valve surgery. We hypothesize that therapy with high dose atorvastatin will significantly reduce the incidence and/or severity of POCD.

NCT ID: NCT01184638 Recruiting - Cognitive Disorders Clinical Trials

Long-term Outcome of General Anesthesia on Dysgnosia

LOGAND
Start date: August 2010
Phase: Phase 4
Study type: Interventional

Cognitive disorders in patients underwent general anesthesia are discussed for decades, but whether there were precise relationship between general anesthesia and dysgnosia is yet to be guaranteed. Although controversial data reported from experimental studies in animals, the investigators still proposed that general anesthetics could impair the normally organized system of the central nervous system, which finally displayed a dysfunction of cognition after general anesthesia in a short- or long-term period. Therefore, different types of general anesthetics such as inhalational anesthetics and intravenous anesthetics, the investigators hypothesized, had a long-term influence on patients' cognitive ability.

NCT ID: NCT01181934 Completed - Schizophrenia Clinical Trials

The Effect of Nicotine on Arousal, Cognition and Social Cognition in Young and Elderly Healthy Subjects.

Start date: May 2010
Phase: Phase 0
Study type: Interventional

This study in young and elderly healthy subjects will investigate the effect of nicotine on arousal, cognitive task and social cognition after acute dose administration.

NCT ID: NCT01181310 Completed - Dementia Clinical Trials

Placebo-Controlled Crossover Study to Evaluate Donepezil and MK-3134 for Reversal of Cognitive Impairment Associated With Scopolamine Administration (3134-005)(COMPLETED)

Start date: June 2007
Phase: Phase 1
Study type: Interventional

The drug, scopolamine, can result in short-term impairments of cognitive function, attention, and memory that resemble those seen in aging and Alzheimer's disease. This study tested the capability of both individual and combined doses of MK-3134 and the current standard treatment: donepezil (Aricept), to reverse such impairments, following a single dose of scopolamine. Participants were evaluated after each of 5 different treatment periods (in a cross-over, double-dummy design): A: placebo to match both donepezil (oral [PO]) and MK-3134 (PO) followed by placebo scopolamine (subcutaneous [SQ]); B: placebo to match both donepezil (PO) and MK-3134 (PO), followed by scopolamine SQ; C: MK-3134 (PO) followed by scopolamine SQ; D: donepezil (PO) followed by scopolamine SQ; E: MK-3134 (PO) and donepezil (PO) followed by scopolamine SQ. The doses of MK3134, donepezil, and scopolamine were the same over all treatment arms in which the specified drug was administered. There were 8 total visits for each treatment period, including 5 Treatment Visits requiring 14-day intervals between visits for study-drug washout. Participants were assessed for cognitive function before and after each treatment period during the Treatment Visits.