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Neurocognitive Disorders clinical trials

View clinical trials related to Neurocognitive Disorders.

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NCT ID: NCT04658394 Completed - Dementia Clinical Trials

Effect of Individual Reminiscence Therapy in the Elderly People With Neurocognitive Disorders

Start date: February 11, 2021
Phase: N/A
Study type: Interventional

This research aims to evaluate the ability of individual reminiscence therapy (RT), using a simple reminiscence format, to improve the overall cognitive function, memory, emotional status and quality of life (QoL) of older adults with neurocognitive disorders (NCD) attending social care and support services. A multicentre randomised controlled trial (RCT) is proposed in Azores archipelago with repeated measures (pre-intervention, post-intervention and follow-up). Intervention group will hold 26 individual RT sessions, twice a week for 13 weeks. Control group participants will maintain their treatment as usual. Make a subsample analysis of the main clinical diagnoses, and compare the results of sample and subsample with a previous study that had the same intervention protocol.

NCT ID: NCT04610515 Active, not recruiting - Clinical trials for Cardiovascular Diseases

Innovative Support for Patients With SARS-COV2 Infections (COVID-19) Registry (INSPIRE)

INSPIRE
Start date: December 15, 2020
Phase:
Study type: Observational [Patient Registry]

The Innovative Support for Patients with SARS COV-2 Infections Registry (INSPIRE) study is a CDC-funded COVID-19 project to understand the long-term health outcomes in recently tested adults, both negative and positive, who have suspected COVID symptoms at the time of their test. Participants will complete short online surveys every 3 months for 18 months, share information about their health using a secure web-based platform, and are compensated for their time.

NCT ID: NCT04600726 Not yet recruiting - Clinical trials for Older Adults With Mild Neurocognitive Disorders

Application of VR-based Working Memory Screening Test

VR
Start date: February 1, 2021
Phase:
Study type: Observational [Patient Registry]

We propose to validate an interactive, immersive spatial memory test from the laboratory test. This VR-based working memory test (VRWMT) is a first-person, self-pacing game embedded within a virtual reality environment, the program is easily implemented with minimal instructions and no supervision that can be community-users friendly. It is specifically designed to assess rapid spatial working memory - a common deficit in all NCD subtypes. Its ability to detect pathological models of dementia, age-related deterioration, and hippocampal dysfunction are well established in literature

NCT ID: NCT04573985 Completed - Clinical trials for Family Caregiver of Patient With Alzheimer Disease

Impact of the Eurékoi Serious Game on Family Caregivers of Patients With a Major Neurocognitive Disorder

Start date: December 8, 2020
Phase: N/A
Study type: Interventional

This study aims to assess the effectiveness of serious EUREKOI gambling on the anxiety of family caregivers of patients with newly diagnosed Alzheimer's disease.

NCT ID: NCT04571502 Not yet recruiting - Alzheimer Disease Clinical Trials

Integration of Health Information Technology and Promotion of Personhood in Family-Centered Dementia Care

Start date: July 2024
Phase: N/A
Study type: Interventional

Alzheimer's disease and related dementias (ADRD) are leading causes of disability and often result in communication deficits of the person with dementia (PWD) that can complicate ADRD caregiving and clinical care. The research team will work with stakeholders to develop and design a personalized Assistive and Alternative Communication (AAC) device that relies on information technology (IT) and touchscreens to promote communication and personhood for PWD about their care preferences and experiences. This study will integrate the AAC into an existing health IT intervention that already facilitates clinical communication between caregivers and providers of PWD, called CareHeroes (CH). A clinical trial will be conducted to evaluate outcomes of 120 triads (PWD/caregivers/providers) utilizing the CH intervention as an adjunct to care and caregiving for 12 months.

NCT ID: NCT04566562 Recruiting - Clinical trials for Postoperative Cognitive Dysfunction

Blood Brain Barrier Dysfunction and Postoperative Neurocognitive Disorders

BBBSx
Start date: August 3, 2020
Phase:
Study type: Observational

Postoperative neurocognitive disorders (PND), which include postoperative delirium and both acute and longlasting neurocognitive deficits, are a significant public health problem, leading to a cascade of deleterious complications. Older adults are particularly at-risk of developing PND both in the short and long term. Although age is consistently reported as an important risk factor, the exact pathophysiology of PND remains poorly understood, but may include postsurgery-compromised blood brain barrier (BBB) function. This project proposes that perioperative BBB dysfunction is associated with measurable brain morphologic findings in cognitive control areas that can be discovered with non-invasive magnetic resonance imaging (MRI). Patients scheduled for surgery with an age range of 65-75 years of age, will participate in brain diffusion-weighted pseudo-continuous arterial spin labeling (DW-pCASL) and diffusion tensor imaging (DTI), cognitive assessments, and evaluation of a BBB marker from blood (at baseline, at two weeks, and at six months after surgery). All patients will have a brain scan (MRI) within before surgery and two weeks and six months after surgery. During this visit cognitive function will be assessed. Patients will also be asked to participate in a blood draw.

NCT ID: NCT04529265 Completed - Clinical trials for Postoperative Delirium

Methylene Blue and Postoperative Neurocognitive Disorders

Start date: May 1, 2021
Phase: N/A
Study type: Interventional

Postoperative Neurocognitive Disorders are the most common neurological complications after major surgery, which are associated with higher increased mortality and morbidity in elderly patients undergoing major surgery. Until now highly effective intervention has not been established yet. Recent preclinical studies suggest mithochiondrial dysfunction may be linked to pathogensis of (postoperative delirium) POD and postoperative cognitive dysfunction (POCD). As Methylene blue(MB) is a mitochondrial protective agent and a safe drug with long history of clinical use, we propose that mitochondrial-targeted interventions may be useful to prevent POD/POCD in surgical patients.

NCT ID: NCT04503798 Recruiting - Clinical trials for Cognitive Dysfunction

Online Cognitive Rehabilitation of Executive Dysfunction in Nonamnestic MCI

Start date: August 20, 2020
Phase: N/A
Study type: Interventional

Nonamnestic mild cognitive impairment (naMCI) is a prodromal state characterized by deficits in executive functioning, a collection of higher-order abilities involved in organization, planning, inhibition, and complex reasoning. Research shows that individuals with naMCI have an increased risk of developing non-Alzheimer's dementia such as frontotemporal dementia and dementia with Lewy bodies, which pose substantial personal and societal costs. Accordingly, interventions that can successfully slow down or reverse the course of naMCI are needed. Goal Management Training (GMT) is a cognitive rehabilitation platform that has been studied extensively, applied clinically, and manualized into kits for clinicians (Levine et al., 2000; Levine et al., 2007; Levine et al., 2011; Stamenova & Levine, 2019). The purpose of GMT is to train individuals to periodically "STOP" what they are doing, attend to task goals, evaluate their performance, and monitor or check outcomes as they proceed. Recently, an online version of GMT has been developed and validated in order to circumvent barriers to attending in-person sessions. The purpose of the current study is to determine if the online version of GMT is effective at improving self-reported executive dysfunction in individuals diagnosed with naMCI against a control group that is receiving treatment-as-usual from their care provider. It is hypothesized that, compared to the control group, individuals receiving GMT will report a decrease in executive function deficits.

NCT ID: NCT04488952 Recruiting - PND Clinical Trials

The Effects of Different Anesthesia Methods on Perioperative Neurocognitive Disorders in the Elderly

Start date: July 8, 2020
Phase: N/A
Study type: Interventional

Perioperative Neurocognitive Disorders(PND) is a common perioperative complication among the elderly, especially in the plastic surgery. Different anesthesia methods have different incidences of PND, but it's still unknow which is better between spinal anesthesia and nerve block combined with general anesthesia. We will apply a psychometric battery test which contain different cognitive domains to estimate the incidence of PND at a week a month and a year after surgery with different anesthesia methods. Study has showed that functional magnetic resonance imaging (fMRI) could detect a cognitive decline through spontaneous neuronal activity in the cortex and hippocampus. In our study, multi-mode imaging technology is used to conduct in-depth research on MRI and make correlation analysis with cognitive function.

NCT ID: NCT04436315 Recruiting - Nursing Home Clinical Trials

Intervention Study of an Individualized Exergame Training for People With Major Neurocognitive Disorder

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

This study evaluates the feasibility of the intervention and the study design.