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Cognitive Dysfunction clinical trials

View clinical trials related to Cognitive Dysfunction.

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NCT ID: NCT02959502 Active, not recruiting - Clinical trials for Major Depressive Disorder

Home-Based CR and tDCS to Enhance Cognition in Persons With Mild Cognitive Impairment and Late Life Depression

Start date: October 31, 2016
Phase: N/A
Study type: Interventional

The overall goals of this project are to assess the feasibility and impact of designing and implementing an at-home intervention aimed at preventing long-term cognitive decline and improving cognition in individuals currently at-risk for developing AD.

NCT ID: NCT02958670 Active, not recruiting - Healthy Clinical Trials

Imaging Tau Deposition in the Brain of Elderly Subjects

Add-Tau
Start date: November 2016
Phase: N/A
Study type: Interventional

Cerebral accumulation of tau and beta-amyloid are major factors of Alzheimer's disease pathology. A novel Positron Emission Tomography (PET) tracer (18-F-AV-1451) now offers the ability to study tau protein deposition in vivo in subjects, in which information on cerebral amyloid deposition has already been gathered. This enables to study effects of tau deposition on neuronal integrity, their relation to effects of beta-amyloid deposition and how this contributes to cognitive impairment or well-being in the elderly.

NCT ID: NCT02951598 Active, not recruiting - Alzheimer Disease Clinical Trials

A Study of Health Care Use and Costs in Participants With Early Stage Alzheimer's Disease (AD)

GERAS-US
Start date: October 29, 2016
Phase:
Study type: Observational

The purpose of this study is to learn about health care use, costs, and clinical outcomes over time for amyloid positive participants with early stages of AD in the United States. This study is for research purposes only, and is not intended to treat any medical condition. No study therapy(ies) for AD will be administered.

NCT ID: NCT02943187 Active, not recruiting - Clinical trials for Mild Cognitive Impairment

Multidisciplinary Intervention for Mild Cognitive Impairment

(MCI)
Start date: October 2016
Phase: N/A
Study type: Interventional

The purpose of this investigation is to conduct a series of case studies on the impact of a novel functional medicine approach to improving cognitive skills, brain structure, and daily functioning for participants with Mild Cognitive Impairment (MCI).

NCT ID: NCT02936219 Active, not recruiting - Clinical trials for Cognitive Impairment

The PREWEAN Study. Weaning of Preterm Infants During the First Year of Life.

PREWEAN
Start date: April 2016
Phase:
Study type: Observational

In this Austrian observational study preterm infants born with a birth weight <1500 g and a gestational age <32 weeks will be investigated at the neonatal outpatient clinic. Infants will be stratified according their feeding regimen (breast, formula and combined feeding) and their introduction of solid foods (early complementary feeding group: <17th week of life corrected for prematurity, late complementary feeding group: ≥17th week of life corrected for prematurity). Nutrient intakes and anthropometric parameters will be assessed at term, 6 weeks, 12 weeks, 6 months, 9 months and 12 months - all corrected for prematurity and with 40, 54 and 66 months.

NCT ID: NCT02920632 Active, not recruiting - Parkinson Disease Clinical Trials

Cognitive Training in Parkinson Study

cogtips
Start date: September 15, 2017
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of an eight-week online cognitive training program on objective and subjective cognitive functions in Parkinson's disease. Moreover, we intend to map the effect on brain network function, and if cognitive training can prevent the development of PD-MCI/PD-D after one- and two-year follow-up. In this study, two training groups will be compared (N: 70 vs 70). In a part of the participants MRI will be assessed (N: 40 vs. 40). We expect cognitive training to improve cognitive functions, and to improve the efficiency of brain network function. Moreover, we expect that cognitive training can decrease the risk of PD-MCI/PD-D at one- and two-year follow-up.

NCT ID: NCT02847403 Active, not recruiting - Dysglycemia Clinical Trials

Long-acting Exenatide and Cognitive Decline in Dysglycemic Patients

DRINN
Start date: February 2016
Phase: Phase 3
Study type: Interventional

The overall objective of the study is to assess the potential effects of the long-acting GLP-1 analogue exenatide in preventing/slowing the progression of cognitive dysfunction and related biomarkers in dysglycemic/prediabetic patients with mild cognitive impairment (MCI).

NCT ID: NCT02781220 Active, not recruiting - Dementia Clinical Trials

Implications for Management of PET Amyloid Classification Technology in the Imaging Dementia(IDEAS) Trial

IMPACT2
Start date: July 2016
Phase:
Study type: Observational

The main purpose of this study is to build upon the evidence captured in the Imaging Dementia - Evidence for Amyloid Scanning (IDEAS; NCT02420756) trial to include valuable information regarding patient-reported outcomes and physician confidence in diagnosis and management based on the Implications for Management of PET Amyloid Classification Technology (IMPACT; NCT number not yet assigned) trial design.

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: 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.