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Cognitive Dysfunction clinical trials

View clinical trials related to Cognitive Dysfunction.

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NCT ID: NCT02738034 Completed - Hypertension Clinical Trials

Cogmed Training Effect in Hypertensive Patients With Cognitive Impairment

Start date: August 2016
Phase: N/A
Study type: Interventional

Systemic arterial hypertension is a disease with high prevalence in several countries, including Brazil. Many studies have correlated hypertension with accelerated loss of cognitive function, especially executive functions. There is some evidence that working memory (WM) is compromised in these populations. However, some computerized training has been developed to rehabilitate the WM, and among them the investigators highlight the Cogmed. Thus, the aim of this study is to evaluate the effects of Cogmed training in the performance of WM and attention of hypertensive patients, as well as the impact of training in the structure and brain function.

NCT ID: NCT02737878 Active, not recruiting - Clinical trials for Mild Cognitive Impairment

Reshaping the Path of Mild Cognitive Impairment by Refining Exercise Prescription

Start date: November 13, 2017
Phase: N/A
Study type: Interventional

Dementia is one of the most pressing health care issues of the 21st century. Evidence suggests that exercise enhances cognitive function in healthy older adults. Most research has focused on aerobic training (AT). Therefore, investigators aim to assess the individual effects of AT and resistance training (RT), as well as the interaction effect of combining the two types of exercise training, on cognitive function in older adults with mild cognitive impairment.

NCT ID: NCT02730013 Completed - Cognitive Decline Clinical Trials

Mind-motor Exercise to Improve Cognition and Functional Fitness

MIND-FUN
Start date: May 2016
Phase: N/A
Study type: Interventional

This is a 3 month cluster randomized controlled trial using a square-stepping exercise program (a.k.a. mind-motor exercise) in retirement and long-term care residences to improve global cognitive functioning in older adults with and without cognitive impairments. The investigators intend this project to be pragmatic and therefore will include residents with dementia and walking aids if the participants wish to participate. The primary outcome is global cognitive functioning, secondary outcomes include: single and dual task gait (only completed with those without dementia), oculomotor functioning, and functional fitness. The investigators hypothesize that there will be improvements in primary and secondary outcomes in the intervention group.

NCT ID: NCT02723318 Completed - Impaired Cognition Clinical Trials

The Impact of Family Financial Support on Cognition

Start date: March 2016
Phase: N/A
Study type: Interventional

The investigators have partnered with financial coaching organizations to establish what the investigators have termed a "Medical-Financial Partnership (MFP)" that offers financial coaching to improve financial and mental health. The investigators will evaluate the MFP's impact on cognition using the Patient Reported Outcomes Measurement Information System (PROMIS) Cognition Short form 8a.

NCT ID: NCT02720445 Active, not recruiting - Clinical trials for Mild Cognitive Impairment

Memory Improvement Through Nicotine Dosing (MIND) Study

MIND
Start date: January 13, 2017
Phase: Phase 2
Study type: Interventional

The purpose of the study is to see if daily transdermal nicotine is able to produce a significant cognitive, clinical and functional improvement in participants with MCI. Neuronal nicotinic receptors have long been known to play a critical role in memory function in preclinical studies, with nicotine improving attention, learning, and memory function. The study will enroll 380 participants for a 2 year period. Participants will be randomized (50:50) to either the transdermal nicotine, beginning at 7mg/day, and increasing to 21mg/day, or placebo skin patch.

NCT ID: NCT02707458 Completed - Clinical trials for Age-related Cognitive Decline

Dosage and Efficacy of Probucol-induced apoE to Negate Cognitive Deterioration

DEPEND
Start date: April 2016
Phase: Phase 1/Phase 2
Study type: Interventional

DEPEND is an open-label but dosage-masked trial of the retired cholesterol-lowering drug probucol as an agent to increase availability of apolipoprotein E (apoE) in the cerebrospinal fluid (CSF) of cognitively intact older persons at risk of Alzheimer's dementia. Absorption of oral probucol is variable. In a sample of 23 cognitively intact persons over age 55, DEPEND will therefore develop an algorithm to prescribe individualized dosing to achieve plasma concentration that will likely increase availability of CSF apoE. These persons will then use their individualized dosage for 12 months to assess longer-term effects of the drug on CSF apoE concentration, while monitoring closely for evidence of adverse consequences of use.

NCT ID: NCT02698982 Completed - Clinical trials for Elderly ; Moderate Risk Surgery

Optimized Anesthesia to Reduce Postoperative Cognitive Impairment in the Elderly

Start date: May 2016
Phase: N/A
Study type: Interventional

The aim of this study is to demonstrate that in elderly and frail patients, a narrower control of intraoperative blood pressure (BP) by the use of a continuous and noninvasive BP monitoring, coupled with an adequate depth of anesthesia, will reduce the incidence of postoperative cognitive impairment and the hospital length of stay.

NCT ID: NCT02677987 Completed - Depression Clinical Trials

The "Light for the Brain" Study

Start date: April 2016
Phase: N/A
Study type: Interventional

Cognitive impairment (such as memory problems) due to cancer and its treatment can interfere with quality of life and can linger long after treatment has ended, yet research examining cognitive rehabilitation approaches has produced limited clinical benefit. The proposed study will provide information about systematic light exposure for the treatment of cognitive impairment in hematopoietic stem cell transplant (HSCT) survivors and will investigate how it works. This study would facilitate the development of this potential treatment, giving health care providers and cancer survivors a much-needed tool to help with cancer-related cognitive impairment.

NCT ID: NCT02676739 Recruiting - Multiple Sclerosis Clinical Trials

Adderall XR and Cognitive Impairment in MS

Start date: May 20, 2016
Phase: Phase 2/Phase 3
Study type: Interventional

This 12 week randomized placebo-controlled study will compare the effects of 10 mg and 20 mg of a mixed amphetamine salt, extended release medication (trade name Adderall XR) to placebo on objective measures of processing speed and memory, as well as on self-reported measures of cognition and quality of life. To be enrolled in the study, MS subjects must demonstrate impaired processing speed on the Symbol Digit Modalities Test (SDMT).

NCT ID: NCT02670161 Enrolling by invitation - Stroke Clinical Trials

Quality Improvement and Practice Based Research in Neurology Using the EMR

Start date: May 2016
Phase: Phase 4
Study type: Interventional

The investigators will conduct at NorthShore University HealthSystem pragmatic trials using the EMR for 10 common neurological disorders. They will demonstrate the feasibility of subgroup based adaptive assignment of treatments, electronic consenting, and outcomes data capture at the point of care using the EMR. They will identify the most effective treatments for common neurological disorders and seek replication by the NPBRN.