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Alzheimer Disease clinical trials

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NCT ID: NCT02330510 Recruiting - Alzheimer's Disease Clinical Trials

Amyloid and Glucose PET Imaging in Alzheimer and Vascular Cognitive Impairment Patients With Significant White Matter Disease

MITNEC C6
Start date: August 2014
Phase:
Study type: Observational

The prevalence of both Alzheimer's Disease (AD) and stroke doubles each decade over 65 years old. Both are major causes of dementia, currently estimated to affect 46 million people worldwide. The current costs globally are $818 billion. Additionally, in population studies elders over 65 years, "covert" cerebral small vessel disease appears on MRI scans as silent lacunar infarcts in 25% as Microbleeds in 10%, and as focal or diffuse 'incidental' white matter disease (WMD) in 95%. WMD is extensive in 20%, with a clinical threshold effect around 10cc2. Small vessel disease is even more common in dementia, often coexisting with AD and independently contributing to cognitive decline and progression to dementia. Longitudinal imaging using cerebral amyloid labeling opens a new opportunity to understand the additive/interactive effects of small vessel disease and AD. The design of this study includes recruitment of two cohorts, including Mild Cognitive Impairment (MCI) and/or early Alzheimer Disease subjects from memory clinics and subjects with strokes/TIA from stroke prevention clinics. Inclusion criteria include the presence of moderate/extensive white matter disease, eg. Fazekas score of 2 (with confluent peri-ventricular hyperintensities) or Fazekas score of 3, as determined by previous MR or CT, > 60 years of age, Mini-Mental Status Exam (MMSE) scores ≥ 20. Subjects will undergo 3T structural MRI (including T1, PD/T2, FLAIR, GRE, DTI, ASL, and resting state fMRI), glucose PET, amyloid PET (using AV-45 florbetapir) and neuropsychological testing, as well as blood sampling. Repeat MR and PET/CT imaging and neuropsychological testing will be conducted at 24 months. The follow up assessments can also be completed at either year 1 or year 3 or Year 4 depending on the availability of study participants. The imaging portion is designed to closely parallel the Alzheimer's Disease Neuroimaging Initiative (ADNI) in order to benefit from the availability of both cognitively normal controls (NC), MCI and Alzheimer's disease subjects with minimal WMD.

NCT ID: NCT02305836 Recruiting - Clinical trials for Cognitive Impairment

Effect of Electroacupuncture Combined With Donepezil for Treating Alzheimer's Disease

Start date: June 2017
Phase: Phase 2
Study type: Interventional

A prospective randomized controlled trial aimed at assessing if electroacupuncture (EA) combined with donepezil is more effective than donepezil for improving the cognitive function of AD patients. The hypothesis of this study is as follow: - Is the short-term effect of EA combined with donepezil better than donepezil on improving cognitive function of patients with Alzheimer's disease after 12 weeks' treatment? - Whether the effect of EA combined with donepezil on improving cognitive function can last until the end of 6 months' follow-up?

NCT ID: NCT02299154 Recruiting - Alzheimer Disease Clinical Trials

Memory Problems Perceptions Among Patients and Accompaniers During Diagnosis Process :

REMAD
Start date: December 2014
Phase: N/A
Study type: Interventional

This study aims to prospectively examine the memory problem perceptions of patients with memory complaints [MCs] and their accompaniers during the diagnostic process.

NCT ID: NCT02288000 Recruiting - Alzheimer Disease Clinical Trials

Prediction of Cognitive Properties of Memantine for Neurodegenerative Diseases

WP3_P002
Start date: September 14, 2016
Phase: Phase 1
Study type: Interventional

The early assessment of new drugs for Alzheimer's disease remains difficult because of the lack of predictive end-point. The use of a battery including different parameters could improve this early development of new drugs. Nevertheless, the interest of such a battery should previously be validated with the yet marketed AD drugs.

NCT ID: NCT02253043 Recruiting - Alzheimer's Disease Clinical Trials

The Safety and Efficacy of Long-term Treatment of PINS Stimulator System for Patients With Alzheimer's Disease

Start date: May 2014
Phase: N/A
Study type: Interventional

Purpose: The purpose of this clinical study is to verify the long term effectiveness and safety of a bilateral deep brain stimulation (DBS) produced by Beijing PINS Medical Co., Ltd. as a treatment option for patients with cognitive, behavioral, and functional disability of Alzheimer's disease.

NCT ID: NCT02247180 Recruiting - Alzheimer's Disease Clinical Trials

Cognitive Rehabilitation in Alzheimer`s Disease

Start date: September 2014
Phase: N/A
Study type: Interventional

This study aims to proof the efficacy of a cognitive rehabilitation program for patients with mild dementia in Alzheimers Disease with respect to activities of daily living.

NCT ID: NCT02227953 Recruiting - Alzheimer's Disease Clinical Trials

A Pilot Study of tDCS for Mild to Moderate Alzhemier's Disease

Start date: August 2014
Phase: N/A
Study type: Interventional

The primary objective of this preliminary study is to investigate whether the transcranial direct current stimulation (tDCS) improves the cognitive function in patients with Alzheimer's disease

NCT ID: NCT02222181 Recruiting - Alzheimer's Disease Clinical Trials

Impact of Pharmacotherapy Management in Patients With Alzheimer's Disease

Start date: April 2014
Phase: N/A
Study type: Interventional

In Brazil, patients with Azheimer's disease (AD) receiving free drugs of government. Even having access to, little is known about the effectiveness, safety and adherence of drug therapy in this group of patients. The research aims to promote adherence and develop strategies to address Drug-Related Problems (DRP's) in AD patients elderly of reference centre for the Elderly of Araraquara . Will be assessed the clinical parameters at the beginning and after the educational intervention period from April 2014 to December 2015.

NCT ID: NCT02208193 Recruiting - Alzheimer Disease Clinical Trials

Alzheimer's Disease, Art and Garden

JAZ ART
Start date: July 2014
Phase: N/A
Study type: Interventional

Gardens and art represent public spaces and support venues of interactions and emotions, seeking not only a variety of conversational themes but also various cognitive skills such as mnemonic skills. The cognitive and psycho-behavioral effects of art and the garden, jointly associated and made available to patients suffering from Alzheimer's disease, need to be evaluated. MAIN OBJECTIVE Delineate the psychological scaffolding virtues of art and garden on cognitive and emotional processes by means of interview analyses in Alzheimer patients and control subjects based on the " art, memory and life " garden. SECONDARY OBJECTIVES Adapt eco-psychosocial approaches of care management to Alzheimer patients: - create assessment methods of: - the therapeutic efficacy of the design of the " art, memory and life " garden, - the perception of an artistic dimension in the living environment of those with Alzheimer's disease, - establish: - workshop applications using art and the garden for therapeutic purposes, - general recommendations for the layout of the garden. PRIMARY ENDPOINT Quantitative data of discursive productions stemming from Interlocutory Logic (Trognon and Batt, 2007, 2010, 2011) for the analysis of interactive behaviors and the assessment of parameters including esthetic appraisals, well-being, mnemonic and emotional processes (frequency and nature of these processes) as well as spatio-temporal orientation. SECONDARY ENDPOINTS - Scores obtained in standard neuropsychological tests, in particular to assess spatio-temporal orientation (Folstein MMSE), - Scores obtained with the " MemoArtZ " tool (MAZ) to evaluate the memorization of artistic elements of the garden, - Scores from the " General Esthetic Preference " (GEP) tool to evaluate the consistency of general esthetic appreciations, - Score obtained with the specific mood assessment scale (CSDD) for subjects in group A, - Score obtained with the specific assessment of emotional events scale (AES) for all subjects. RESEARCH METHODOLOGY Open, monocentric, controlled (group of healthy control subjects) study. Population: 2 groups: Group A "Alzheimer group": patients with mild to severe stages of Alzheimer's disease: subgroup A1 "Alzheimer group hospitalized at the Paul Spillmann Centre (Centre Paul Spillmann, CPS)" (CHU de Nancy, France); subgroup A2 "Alzheimer group monitored at the Resource and Research Memory Centre (Centre Mémoire de Ressources et de Recherche, CMRR)" (CHU de Nancy, France) Group B "healthy control group": healthy volunteers Therapeutic fallouts of this study will benefit Alzheimer patients in terms of better care management, notably: i) by determining the design, conception and layout of the gardens destined to these patients, ii) by developing the introduction of an artistic dimension to the design of such healing gardens and in their living environment, iii) by establishing workshop application perspectives using the contemplation of works of art and the garden for therapeutic purposes.

NCT ID: NCT02204969 Recruiting - Alzheimer Disease Clinical Trials

LIWA for Treatment of Alzheimer Patients

LIWA
Start date: January 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The thermal therapy combined with magnetic fields and ozone has a direct effect on patients with dementia and Alzheimer's with a regression of more than 60% of them