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Cognition Disorders clinical trials

View clinical trials related to Cognition Disorders.

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NCT ID: NCT00594633 Completed - Brain Tumor Clinical Trials

Adjunctive Donepezil Therapy and Genetic Risk Factors of Cognitive Dysfunction in Brain Tumor Survivors

Start date: October 2004
Phase: Phase 1
Study type: Interventional

A significant number of brain tumor patients who received radiation or chemotherapy have thinking problems as a result of their treatment. The purpose of this study is to find out if treatment with Aricept (donepezil) may improve some aspects of thinking abilities in patients with brain tumors who received radiation or chemotherapy. This research will also study whether persons having particular genes for a blood-borne substance called apolipoprotein E (APOE) are more likely to have thinking problems after radiation or chemotherapy treatment for their brain tumors. The findings of this study will help us find out whether Aricept can improve thinking abilities after cancer treatment, and whether some of the thinking difficulties may be in part related to having certain genes.

NCT ID: NCT00586066 Completed - Bipolar Disorder Clinical Trials

Memantine and Cognitive Dysfunction in Bipolar Disorder

Start date: November 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to see whether memantine improves memory function in participants with bipolar disorder who have minimal symptoms. Secondary analyses will test the role of memantine in improving residual mood symptoms (depression and mania) in participants with bipolar disorder. We hypothesize that in participants with bipolar disorder who have minimal symptoms memantine will be effective in improving cognitive functions, as measured by the difference in neuropsychological test scores at the beginning and at the end of the trial.

NCT ID: NCT00582491 Completed - Cocaine Dependence Clinical Trials

Modafinil, Sleep, and Cognition in Cocaine Dependence

Start date: August 2006
Phase: N/A
Study type: Interventional

Subjects participating in this protocol will participate in three phases: 1) pre-admission, 2) inpatient admission, and 3) follow-up. Pre-admission involves screening (detailed in inclusion/exclusion criteria section) and one week of outpatient sleep and activity monitoring. Inpatient admission is 16 consecutive nights on the Clinical Neuroscience Research Unit and involves subjective and objective tests of sleep, sleepiness, attention, and learning. During inpatient admission subjects will take modafinil or placebo. For follow-up, subjects will return to the CNRU for one night and again participate in objective tests of sleep, sleepiness, attention, and learning. We hypothesize that modafinil will decrease subject and objective measures of sleepiness and will promote attention and learning in cocaine dependent persons.

NCT ID: NCT00567203 Completed - Schizophrenia Clinical Trials

A Study Of Adjunctive Treatment Of Cognitive Deficits In Schizophrenia

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

The objective of this study is to evaluate the safety, tolerability, and efficacy of two dose regimens of PF-3463275 compared with placebo added to ongoing atypical antipsychotic therapy for cognitive deficits in subjects with chronic symptoms of schizophrenia.

NCT ID: NCT00567060 Completed - Memory Disorders Clinical Trials

Efficacy and Safety of Piracetam Taken for 12 Months in Subjects Suffering From Mild Cognitive Impairment (MCI)

Start date: May 2000
Phase: N/A
Study type: Interventional

The purpose of this study was to explore in a more documented way the relative potential and efficacy of piracetam 9600 and 4800 mg daily.

NCT ID: NCT00564902 Completed - Clinical trials for Age Related Macular Degeneration

The Zeaxanthin and Visual Function Study

ZVF
Start date: November 2007
Phase: N/A
Study type: Interventional

To evaluate if supplementation of zeaxanthin (with or without Lutein) is beneficial to patients with early and moderate Atrophic Age Related Macular Degeneration.

NCT ID: NCT00546767 Completed - Clinical trials for Mild Cognitive Impairment

Home-Based Assessment for Alzheimer Disease Prevention

HBA
Start date: September 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate three methods of performing home-based assessments in Alzheimer's Disease (AD) prevention trials. The initial in-person assessment will be done in the clinic or at home.

NCT ID: NCT00545155 Completed - Depression Clinical Trials

Screening and Interventions in an Acute Care Setting

Start date: June 2007
Phase: N/A
Study type: Observational

The purpose of this study is to: 1) evaluate the reliability and validity of EMS screening for depression and cognitive impairment and 2) to develop a pilot ED intervention program to address the needs of older adults found to be at risk for depression and cognitive impairment.

NCT ID: NCT00544856 Completed - Alzheimer's Disease Clinical Trials

Effects of a Complex Cognitive Training in Mild Cognitive Impairment and Mild Alzheimer's Disease

Start date: October 2007
Phase: N/A
Study type: Interventional

A recent meta-analysis that included over 29.000 individuals found that the odds ratio (OR) of individuals with high brain reserve compared to low was 0.54 (p < 0.0001), a risk decrease of 46%. Among the factors that influence cognitive reserve, mentally stimulating activities was the most robust factor after controlling for education, age, occupation and other potential confounds. The brain reserve effect was sustained over a median longitudinal follow-up of 7 years. It would be interesting to detect whether a complex cognitive training could show similar effects on the cognitive abilities of patients with mild Alzheimer's disease (AD) and mild cognitive impairment (MCI) as it has been reported in previous studies based on mentally stimulating activities analysis. The hypothesis is that a complex cognitive training alters the neural networks in both subject groups and this alteration is associated with improvement or stabilization of cognitive and non-cognitive function. The investigator will perform a complex cognitive training program. Twenty patients with mild AD and twenty four patients with MCI will be recruited in this study. The patients will be randomised in control- and treatment groups.Additionally indirect effects on non-cognitive functions will be evaluated in caregivers of the patients. The investigators expect that the cognitive and non-cognitive abilities will be changed during the cognitive training. The investigators also expect differences between treatment and control groups.

NCT ID: NCT00539305 Completed - Clinical trials for Mild Cognitive Impairment

Hormone and Information Processing Study

HIP
Start date: July 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to examine the effects of testosterone (T) replacement on changes in thinking and memory, as well as mood in older men with mild cognitive impairment (MCI) and low T levels. The study will also examine whether taking testosterone has effects on biological markers related to Alzheimer's disease.