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Cognitive Decline clinical trials

View clinical trials related to Cognitive Decline.

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NCT ID: NCT01264614 Completed - Dementia Clinical Trials

Effects of Strengthening Exercise on the Brain for Early Dementia and Normative Older Adults

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

This study will evaluate the effects of low-intensity strengthening exercise on the brain (thinking and processing speed) for patients with early dementia, compared with normative older adults. Participants will engage in 3 months of exercise 3-5 times per week using a chair and small weights. It is hypothesized that there will be a significant improvement in brain function.

NCT ID: NCT01132261 Completed - Cognitive Decline Clinical Trials

Trial of a Brain Preservation Diet in Preventing Cognitive Decline in Old Age Hostel Residents

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

Dementia is a major cause of disabilities in older people. If the onset of dementia can be delayed by preventive measures, the burden of the disease to the society can be greatly reduced. It is now recognised that dietary factors are related to the incidence of dementia. High intake of vegetables, fruit and fish are protective while high intake of saturated fat and salt (via its effect on blood pressure) are detrimental to risk of dementia. The investigators therefore propose to perform a randomized controlled trial of dietetic interventions in old age hostels in Hong Kong. Twelve old age hostels under the Tung Wah Group will be randomly assigned to intervention or control groups. The intervention group will receive dietetic interventions by 2 weekly small group discussion with the residents, modification of menu and publicity. The daily diet to be implemented consists of the following principles: 1. fresh fruit 2 portions, 2. vegetables 4 portions, 3. fish, 4. white meat, 5. sodium intake < 100 mmol/L, 6. six glasses of water. In the control group. The dietician will give two health talks and advice on menu only. The primary outcome is the incidence of questionable dementia in those who are normal at baseline and the incidence of dementia in those who have questionable dementia at baseline. The categorisation will be performed by trained research assistant after administering a structured questionnaire. Change in mini-mental examination score and SF36 quality of life scores are secondary outcomes. Food records over three days for each subject are recorded every three months, to ensure that the brain preservation diet has been adhered to. Half of the subjects will be randomly assigned to have blood and urine tests at baseline and at one year, in order to examine the health effects of dieting.

NCT ID: NCT01109836 Completed - Dementia Clinical Trials

Austrian Polyintervention Study to Prevent Cognitive Decline After Ischemic Stroke

ASPIS
Start date: June 2010
Phase: Phase 4
Study type: Interventional

Aim of this randomized controlled study is to test if intensive polyintervention therapy including life style modifications targeting at reduction of modifiable risk factors of stroke can reduce the risk of post-stroke cognitive decline compared to a group of patients receiving standard care.

NCT ID: NCT01045031 Active, not recruiting - Cognitive Decline Clinical Trials

Cognitive Function in Elderly Marathon Runners

APSOEM
Start date: December 2008
Phase:
Study type: Observational

There is substantial research on the effects of physical exercise on cognitive functions. However, less attention has been paid on the requirements of training intensity and length to enhance cognitive abilities in the elderly. To the investigators knowledge no studies have evaluated the effects of extensive endurance exercise training on cognitive functions by studying elderly marathon runners and bicyclists. On the basis of the scientific literature published so far it is not known whether the beneficial impact of endurance exercise training depends on the intensity of training. The investigators therefore designed a cohort study with adequate power in order to evaluate the effects of intensive endurance exercise training on cognition. This trial, an Austrian prospective cohort study in cognitive function of elderly marathon-runners (APSOEM) is being conducted and will compare neuropsychological performance outcomes of elderly marathon runners or bicyclists with controls matched concerning age, education years, occupation, and verbal intelligence.

NCT ID: NCT00938964 Completed - Cognitive Decline Clinical Trials

Lidocaine For Neuroprotection During Cardiac Surgery

Start date: July 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to see if a drug called lidocaine prevents cognitive injury (a decline in mental abilities) after heart surgery. Lidocaine is currently FDA approved and is commonly used for treating some heart rhythm disorders and for regional anesthesia (blocking nerves). The investigators are enrolling subjects in this research project to see if lidocaine will reduce the high incidence of cognitive injury seen after heart surgery. As part of this study, the investigators will also evaluate the relationship between cognitive injury and genetic makeup and the chemical changes in the subjects blood during and after surgery.

NCT ID: NCT00924937 Completed - Diabetes Mellitus Clinical Trials

CORonary Diet Intervention With Olive Oil and Cardiovascular PREVention

CORDIOPREV
Start date: November 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects of the consumption of two different dietary patterns (low fat versus Mediterranean Diet) on the incidence of cardiovascular events of persons with coronary disease.

NCT ID: NCT00852358 Completed - Cognitive Decline Clinical Trials

A Study of Intrathecal Enzyme Therapy for Cognitive Decline in MPS I

Start date: June 2009
Phase: N/A
Study type: Interventional

This is a 24-month study of the use of laronidase administered into the spinal fluid to treat cognitive decline in mucopolysaccharidosis I (MPS I). MPS I is a rare genetic condition due to deficiency of the enzyme alpha-l-iduronidase. Laronidase is the manufactured form of the enzyme alpha-l-iduronidase. MPS I is a heterogeneous disease with several clinical phenotypes ranging from the most severe, Hurler syndrome, to the attenuated forms, Hurler-Scheie and Scheie. Although patients with milder forms of MPS I may not have grossly observable problems with cognition, these patients do have learning difficulties that are apparent in school and with neuropsychological testing. The goal of this study is to evaluate whether intrathecal recombinant human alpha-l-iduronidase (rhIDU) injections can stabilize or improve cognitive decline in individuals with MPS I.

NCT ID: NCT00715845 Terminated - Clinical trials for Cardiovascular Disease

Carbon Dioxide Insufflation on Cerebral Microemboli

Start date: April 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if blowing carbon dioxide into the surgical field during open-heart surgery to displace retained chest cavity air from the atmosphere will decrease the number of microembolic being introduced into the heart chambers and brain.

NCT ID: NCT00704327 Terminated - Cognitive Decline Clinical Trials

Evaluating the Impact of Cerebral Ischemic And Degenerative Changes On Cognition

Start date: February 2008
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate whether or not cerebral atrophy scores obtained from a brain MRI can correlate with Cognitive Test results. These results hope to demonstrate a link between cerebral ischemic/degenerative changes shown on the MRI and cognition functions results.

NCT ID: NCT00696514 Unknown status - Osteoporosis Clinical Trials

Vitamin B12 and Folic Acid Supplementation for Preventing Fractures in Elderly People

B-PROOF
Start date: September 2008
Phase: Phase 1
Study type: Interventional

It is hypothesized that vitamin B12 and folic acid supplementation reduces the number of incident fractures. The proposed study, a randomized placebo-controlled intervention trial, compares daily supplementation with folic acid (400 mcg) and vitamin B12 (500 mcg) to a placebo for a period of two years or longer in 3000 men and women aged 70 years and older, with initial basal plasma total homocysteine (tHcy) levels >= 15 micromol/L. Fracture incidence and time to fracture will be assessed and used as the efficacy measure. Metabolic studies in a sub sample of the population will be included aiming to contribute to an understanding of the biological mechanisms underlying the associations found between markers of B-vitamin status and bone quality.