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Dementia clinical trials

View clinical trials related to Dementia.

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NCT ID: NCT03875326 Recruiting - Clinical trials for Mild Cognitive Impairment

Stimulation to Improve Memory

STIM
Start date: April 1, 2019
Phase: N/A
Study type: Interventional

This study will test the effects of different doses of a form of non-invasive brain stimulation for the treatment of individuals with mild cognitive impairment (MCI) and dementia of the Alzheimer's Type (DAT).

NCT ID: NCT03861884 Recruiting - Clinical trials for Dementia (Diagnosis)

Cognition and NeuroImaging in neuroDegenerative Disorders (CogNID)

Start date: December 12, 2018
Phase:
Study type: Observational

This prospective study aims: 1. to compare cognitive performance in different clinical groups of participants with mild cognitive impairment (MCI) or mild dementia [Alzheimer's Disease (AD), Vascular Cognitive Impairment (VCI) and Fronto-temporal Dementia (FTD)] to determine whether scores reveal differential profiles between the groups, 2. to demonstrate differences in imaging markers between different dementia syndromes and healthy volunteers using ultra high-field MRI at 7T.

NCT ID: NCT03846492 Recruiting - Alzheimer Disease Clinical Trials

Targeting Brain Physiology to Treat Neuropsychiatric Symptoms of Dementia Using TMS-EEG and tDCS

tTED
Start date: April 24, 2019
Phase: N/A
Study type: Interventional

Agitation and aggression impose a tremendous burden on the individuals living with dementia, their families, caregivers, and healthcare systems. Neuropsychiatric symptoms of dementia (NPS) affect up to 80% of patients with Alzheimer's dementia (AD). The mechanisms of agitation in AD are poorly understood and the current interventions are only modestly effective while having serious adverse effects. In this study, the investigators propose to assess the mechanisms and treatment of neuropsychiatric symptoms in AD with the use of non-invasive, brain stimulation approaches. By applying magnetic stimulation to the surface of the head (transcranial magnetic stimulation - TMS) combined with electroencephalography (EEG), the investigators will be able to study the mechanisms of agitation and advance our understanding of AD. Further, the investigators will evaluate if transcranial direct current stimulation (tDCS) is effective to treat agitation dementia.

NCT ID: NCT03822286 Recruiting - Dementia Clinical Trials

Development and Evaluation of E-training and Mentoring Support Program on Dementia Care for Home-care Workers

Start date: January 30, 2019
Phase: N/A
Study type: Interventional

This study evaluate the effects of three-month dementia care e-training and mentoring support program on home-care workers using a two-group randomized controlled trial.

NCT ID: NCT03775772 Recruiting - Dementia Clinical Trials

Oral Health, Bite Force and Dementia

OrBiD
Start date: December 13, 2018
Phase: N/A
Study type: Interventional

Study aims: The primary aim is to identify influencing variables on oral hygiene / oral health and bite force in patients with dementia.

NCT ID: NCT03761381 Recruiting - Alzheimer Disease Clinical Trials

OCT Angiography and NRAI in Dementia

Start date: September 14, 2018
Phase:
Study type: Observational

The primary goals of this study are to use optical coherence tomography (OCT) angiography (blood vessel mapping) to: 1. Detect retinal blood vessel and blood flow changes in participants with dementia. 2. Detect amyloid protein deposits in the retinas of participants with dementia.

NCT ID: NCT03754725 Recruiting - Dementia Clinical Trials

Ferritin and Iron Burden in SAH sIRB

Start date: October 1, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

Ruptured cerebral aneurysms lead to subarachnoid hemorrhage (SAH),that has a high morbidity and mortality rate, the severity of which is predicted by the "Hunt-Hess grade" (HHG). SAH leads to iron (Fe) and hemoglobin (Hb) accumulation in the brain, which is toxic for neurons. Ferritin (iron reported in the brian) and iron overload leads to brain atrophy, specifically in the mesial temporal lobe (hippocampus, impairing patients' cognition. It is estimated that 50% of survivors have cognitive deficits. Most of the survivors of SAH could not return to work. Iron chelation therapy has been recently gaining ground as a therapeutic intervention in intraparenchymal hemorrhage and in SAH. However, there has not been any study that assess the iron deposition in the brain and the level of ferritin in the cerebrospinal fluid of SAH patients. The investigators propose to conduct a randomized trial using Deferiprone (oral chelating agent, "De") + standard of care versus standard of care in patient with SAH to: 1. assess the level of ferritin (Ft) in CSF (CSF withdrawn from ventriculostomy tube), 2. assess functional outcomes measured by the Montreal Cognitive Assessment (MoCA) score, a score used to assess the level of dementia, mainly in Alzheimer disease patients. 3. quantify the the total iron deposition in the brain based on MRI

NCT ID: NCT03753191 Recruiting - Dementia Clinical Trials

The Effects of Transcranial Direct Current Stimulation on Executive Function in People With Mild to Moderate Dementia

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

To study the effects of transcranial direct current stimulation on executive function in people with mild to moderate dementia

NCT ID: NCT03724344 Recruiting - Dementia Clinical Trials

Correlation Study Between Mental Behavioral Symptoms in Dementia Patients and Mood Disorders of Caregivers

Start date: October 20, 2017
Phase:
Study type: Observational [Patient Registry]

Traditionally, the more severity of dementia patients, the heavier the burden of the comparators, and in the clinical observation,the dementia patients with rich mental behavior symptoms are more burdened. Therefore, exploring the impact of psychological burden and different subtypes of different dimensions with Behavioral and psychological symptoms (BPSD) will more comprehensive understanding of the factors affecting the burden of caregivers. The starting point of this project is to analyze the relationship between the types of mental behavior symptoms of dementia patients and the emotional disorders of caregivers. The topic will analyze the correlation of psychological burden of caregivers and different symptom dimensions from the perspective of refinement, helping more effective identifying high-burden mental behavior symptoms in clinically , judging the risk of emotional problems in caregivers, and adopting better humanities or medical care, so that dementia patients can better adapt to care and improve the mental health of caregivers.

NCT ID: NCT03702907 Recruiting - Alzheimer Disease Clinical Trials

DC Longitudinal Study on Aging and Specimen Bank

(DC LSOA)
Start date: January 1, 2007
Phase:
Study type: Observational

The Georgetown University Memory Disorders Program, part of the Department of Neurology, is conducting pilot studies of the feasibility of various diagnostic tests for Alzheimer's disease, mild cognitive impairment and other neurodegenerative diseases. Further, this study is assessing longitudinal changes in biological, lifestyle, and cognitive assessment collection. The primary goal of this study is to examine the feasibility of biochemical assays, genetic testing, and cognitive and lifestyle assessments in the ante-mortem diagnosis of Alzheimer's disease, mild cognitive impairment and other neurodegenerative diseases. This research involves genetic and cognitive status testing but the findings will not be shared with research subjects. This will be accomplished ex vivo using blood, and/or cerebrospinal fluid (CSF) specimens from patients with a diagnosis of probable Alzheimer's disease, mild cognitive impairment, or other neurodegenerative diseases and from normal controls.