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Dementia clinical trials

View clinical trials related to Dementia.

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NCT ID: NCT01192529 Recruiting - Parkinson's Disease Clinical Trials

Evaluation of a Diet in Patients With Senile Dementia

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

The most common symptoms associated to senile dementia disease are confusion about schedules, hyperactivity... In this sense, these patients have frequently poor nutrition, resulting in malnutrition problems or malnutrition high risk.

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: NCT01182987 Recruiting - Dementia Clinical Trials

SCAN Memory Program Evaluation Study

SMPES
Start date: October 2009
Phase: N/A
Study type: Interventional

The SCAN Memory Program Evaluation study is an evaluation of a randomized controlled trial intervention consisting of a care management program for cognitively-impaired health plan members and for their informal/family caregivers. The program includes collaboration between the health plan, partnering medical groups, and community organizations. Program activities include: 1) telephonic-structured assessments with informal caregivers conducted by SCAN Memory Program care managers; 2) problem identification as a result of these assessments; and 3) pre-established protocols and procedures for problem resolution. ACCESS, the prototype for the SCAN Memory Program, was developed and tested in San Diego County and was very successful in helping affected patients and their caregivers.

NCT ID: NCT01147679 Recruiting - Alzheimer's Disease Clinical Trials

Study of Social Behavior and Emotion in Frontotemporal Dementia, Alzheimer's Disease and Controls

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

This study is designed to document the loss of sociomoral emotions (like empathy, guilt, and embarrassment) in patients with behavioral variant frontotemporal dementia. The loss of these emotions, which function as the motivators for social behavior, will manifest in specific interpersonal behaviors. These behaviors will correlate with regional changes in regional changes in medial frontal and anterior temporal lobes. These social and emotional changes will be compared with a young-onset Alzheimer's disease comparison group.

NCT ID: NCT01126775 Recruiting - Stroke Clinical Trials

Neuro-Prävention im Rahmen Des Interventionsprojektes INVADE-2 (Follow-up Studie)

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

"Silent" strokes are more frequent than clinical apparent strokes and can be detected noninvasively by MRI-investigations of the brain. Persons with silent strokes have a considerably increased risk for clinical apparent strokes as well as for the development of dementia. Intention of the study is the detection of silent strokes and microbleedings by standardized cranial MRI in 1000 participants (500 high-risk and 500 low-risk persons for cerebrovascular accidents) after a standardized neurological and neuropsychological examination. Results will be the base of early detection and early preventive strategies of cerebrovascular accidents in high-risk persons. In the course of a systematic follow-up examination without MRI the same 1000 patients (500 high-risk and 500 low-risk persons for cerebrovascular accidents) will be reinvited to the sites. In addition to the standardized neurological and neuropsychological examinations a surrogate parameter of nephropathy, microalbumin, will be examined as this parameter could be helpful in forecasting cerebral microangiopathy. The clinical investigation will be expanded by several tests in order to assess symptoms of cerebral microangiopathy.

NCT ID: NCT00892086 Recruiting - Depression Clinical Trials

Prevalence and Recognition of Geriatric Syndrome in Outpatient Clinic at Srinagarind Hospital

Start date: May 2009
Phase: N/A
Study type: Observational

The purpose of this study is to collect the prevalence of geriatric syndrome, which is recognized by an internist, and to compare the data based on the comprehensive geriatric assessment by a geriatrician. The secondary outcome is to develop a practical collected form for the internist.

NCT ID: NCT00878280 Recruiting - Dementia Clinical Trials

Copy Number Variations, Inflammatory Cytokines and the Risk of Dementia

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

Assess the association of copy number variation (CNV) and inflammatory cytokine with the risk of dementia.

NCT ID: NCT00866099 Recruiting - Dementia Clinical Trials

Dementia Early Recognition and Response in Primary Care

EVIDEM-ED
Start date: July 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to develop and test an educational intervention for dementia in primary care, combining timely diagnosis, psychosocial support around the period of diagnosis and management concordant with guidelines.

NCT ID: NCT00820859 Recruiting - Dementia Clinical Trials

Treatment Routes for Exploring Agitation

TREA
Start date: June 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the efficacy of non-pharmacological ways to treat agitated behaviors in nursing home residents with dementia. The hypothesis is that non-pharmacological interventions will be more effective than placebo in decreasing such behaviors.

NCT ID: NCT00743418 Recruiting - Dementia Clinical Trials

Tracking Technologies for the Analysis of Mobility in Alzheimer's Disease

SenTra
Start date: June 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The research is aimed at exploring the application of novel tracking technique for the study of spatial activity among dementia patients and its implication on their families. The study sample will be composed of three groups of volunteers, each including100 participants aged over 60 years. The first group will include MCI (Mild Cognitive Impairment) patients. The second group will include patients that suffer from mild dementia. The third group will include age matched healthy participants. The tracking equipment will be a GPS apparatus of 450 gms that will be carried by the participants for 24 hours along 2-4 weeks. The GPS data will be transferred via the cellular network to operator center at the Hebrew university at Jerusalem, and will be documented in assigned data files. This monitoring procedure will be held every year and along a period of five years. The impact of the patient behavior on the care giver will be studied by means of five interviews along the tracking period.