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Cognitive Impairment clinical trials

View clinical trials related to Cognitive Impairment.

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NCT ID: NCT04033952 Active, not recruiting - Stroke Clinical Trials

Strategy Training on Improving Executive Functions in Persons Following Acquired Brain Injury

Start date: May 29, 2018
Phase: N/A
Study type: Interventional

About two-third individuals with acquired brain injury (ABI) experience cognitive impairments. Deficits in executive functions is one of the most prevalent cognitive impairments following ABI which result in decline of recovery and independence. Lack of intervention shows evidence of immediate and long-term effect on executive function which is critical after returning to the community. The overall aim of this study is to examine the efficacy of strategy training intervention on executive functions and participation on community-dwelling people with ABI. Findings of the study will provide unequivocal evidence on the duration of effectiveness of strategy training and support the development and application of the program in rehabilitation practice.

NCT ID: NCT04033510 Recruiting - Atrial Fibrillation Clinical Trials

Acute Cognitive Changes During Atrial Fibrillation Episodes (AFCOG)

AFCOG
Start date: August 14, 2019
Phase:
Study type: Observational

Objectives: - First, to determine if patients with a history of AF have acute measurable changes in cognitive functioning while in an episode of AF. - Second, to collect basic insight into what specific physiologic (blood pressure, pulse oximetry, heart rate, temperature) and pharmacologic (antiarrhythmic medications, rate control medications, anticoagulants, antiplatelet medications, etc.) factors minimize the neurological impact on patients while they are in AF. It is hypothesized that when using a tablet-based cognitive testing software - Cambridge Cognition (specifically to assess executive function, learning and working memory: Rapid Visual Information Processing test, Spatial Working Memory/Spatial Span Task tests, One touch Stockings of Cambridge test, Cambridge Gambling Task, Multitasking Test/Intra-Extra Dimensional Set shift tests) - a significant difference will be noted between how the patients perform while in atrial fibrillation compared to the patients' performance while in normal sinus rhythm.

NCT ID: NCT04027400 Recruiting - Breast Cancer Clinical Trials

Effects of Computer-Assisted Cognitive Rehabilitation Programs With Breast Cancer Survivors

Start date: February 26, 2018
Phase: N/A
Study type: Interventional

Potential study participants will be recruited at breast cancer survivor support groups. Informed consent will be obtained with a form approved by the TWU IRB and participants will complete 4 tests. Then participants will be randomly assigned to one of two computer-assisted cognitive programs. Participants will be sent by email, exercises specific to their assigned computer-assisted cognitive program from Happyneuron Pro (http://ie.scientificbraintrainingpro.eu/). Cognitive training on the computer entails 30 minutes a day, five times a week for one month. At the end of the study, the four pretests will be repeated, a satisfaction survey administered.

NCT ID: NCT04027244 Recruiting - Clinical trials for Coronary Artery Disease

Leg Ischaemia Management Collaboration

LIMb
Start date: May 10, 2019
Phase:
Study type: Observational

Single-centre prospective cohort study of patients presenting with severe limb ischaemia (SLI). The primary outcome measure will be 12 month major amputation rate. A historical cohort of patients identified retrospectively will be the comparitor group used to assess the impact of a newly-established rapid-access limb salvage clinic. Primary aim: - Determine the proportion of patients with SLI undergoing major lower limb amputation within 12 months of presentation. Secondary aims: - Assess clinically important short-, medium- and long-term outcomes in those undergoing and not undergoing amputation - Prevalence and degree of frailty and cognitive impairment - Pevalence and degree of cardiac disease (detected by stress MRI) - Establish a biobank for future biomarker analysis - Investigate the role of frailty and cognitive assessments, cardiac MRI and biomarkers in risk-stratification of patients with SLI

NCT ID: NCT04026048 Completed - Cancer Clinical Trials

Online Treatment of Cognitive Impairment and Insomnia in Cancer Survivors

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

The investigators will answer the question of whether treating insomnia using Cognitive Behavior Therapy for Insomnia (CBT-I) can improve perceived cognitive impairment (PCI) in cancer survivors compared to a waitlist control group. The investigators will recruit 124 people with insomnia and cognitive complaints who have completed cancer treatment at least 6 months prior to the study.

NCT ID: NCT04012086 Completed - Parkinson Disease Clinical Trials

Physical Therapy and Cognitive Decline

PD-MCI
Start date: September 15, 2015
Phase: N/A
Study type: Interventional

Background: Mild Cognitive Impairment in Parkinson's disease (PD-MCI) is considered a predictor for the development of dementia, a major source of eventual treatment-refractory disability. Physical activity, which has proved effective in improving motor symptom, has also been proposed as a possible non-pharmacological intervention for preventing/delaying the onset of cognitive impairment in Parkinson's disease (PD). Objectives: This study evaluates the effect of a 4-week rehabilitation therapy on cognitive functions in mid-stage PD-MCI patients. Methods: 40 PD-MCI patients were randomized to receive physical therapy (PT) or no physical therapy (CT) according to a controlled single-blind design. Subjects in the PT group (n. 17) attended a rehabilitation program with 6 sessions/week, each lasting 60 minutes, for 4 weeks in addition to their usual pharmacological therapy; subjects in CT group (n. 22) received only pharmacological therapy. Cognitive and motor functions were assessed at baseline (T0) and at the end of the intervention period (T1) in both groups.

NCT ID: NCT04005313 Recruiting - Clinical trials for Cognitive Impairment

Development and Application of Portable Multisensory Stimulation Device

Start date: January 2017
Phase: N/A
Study type: Interventional

This is a study to develop the vibroacustic devices, and to compare the effects between vibroacustic device therapy and music therapy in adults with dementia or with neck pain. The immediate effect and long-term training effect would be assessed.

NCT ID: NCT03982147 Active, not recruiting - Stroke Clinical Trials

White Matter Connections and Memory: the STRATEGIC Study

STRATEGIC
Start date: April 11, 2014
Phase:
Study type: Observational

In patients who have had a stroke, memory problems are common. Some patients with memory problems improve over the first year after stroke, but recovery is unpredictable. The STRATEGIC study assesses patients with recent stroke and follows them up after one year. The study uses cognitive testing and advanced MRI to understand the brain's mechanism for recovery from memory problems and to identify factors that may predict later recovery.

NCT ID: NCT03981380 Enrolling by invitation - Alzheimer Disease Clinical Trials

11C-PIB PET Study in MESA at Columbia University

Start date: August 1, 2020
Phase:
Study type: Observational

The investigators will conduct a study of brain positron emission tomography (PET) using 11C-PIB for the imaging of brain amyloid in 250 participants in the Multiethnic study of atherosclerosis (MESA) at Columbia University Irving Medical Center in New York City. Participants will be imaged only once with Pittsburgh Compound B (PIB) PET.

NCT ID: NCT03972384 Completed - Critical Illness Clinical Trials

A Problem Solving Intervention for Post-ICU Cognitive Impairment in Older Adults

PIC-UPS
Start date: January 21, 2022
Phase: N/A
Study type: Interventional

This study will apply an evidence based program to assist ICU survivors to overcome cognitive problems as a result of their critical illness. This study will determine feasibility of recruitment, retention and engagement with the program as well as acceptability of the program to the participants.