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Age-Related Cognitive Decline clinical trials

View clinical trials related to Age-Related Cognitive Decline.

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NCT ID: NCT03162913 Completed - Obesity Clinical Trials

The Effects of Strawberry Supplementation on Memory and Gait Among Over-weight Older Adults

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

This study is being conducted to assess the effect of dietary strawberry supplementation on cognition and mobility in obese middle-aged and older adults. It is hypothesized that plant compounds, present in strawberries, may improve cognition and mobility.

NCT ID: NCT03056508 Terminated - Clinical trials for Age-Related Cognitive Decline

Lifestyle, Exercise and Diet: The LEAD Study

LEAD
Start date: July 1, 2018
Phase: N/A
Study type: Interventional

This study will explore the impact of an exercise and nutrition (EX+NUTR) , relative to exercise alone (EX) intervention, on brain structure and function as well as blood biomarkers in older adults with subjective cognitive decline (SCD) and vascular risk factors. The overall hypotheses are that a combined EX+NUTR, relative to EX, intervention will evoke more positive changes in brain structure (e.g. hippocampal volume), neural activity (e.g. task associated functional activations monitored through fMRI), and cognitive performance. These changes will be associated with an improved metabolic profile, reductions in inflammatory cytokines and oxidative burden, and greater intervention compliance.

NCT ID: NCT02922920 Completed - Clinical trials for Cardiovascular Risk Factors

Effects of Tart Cherry Juice on the Body

Start date: November 2014
Phase: N/A
Study type: Interventional

Tart cherries are a rich source of antioxidants. Studies have shown that tart cherries exert anti-oxidative and anti-inflammatory properties. The purpose of this study is to learn about the effects of drinking tart cherry juice on cardiovascular and cognitive health.

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: NCT02665481 Completed - Clinical trials for Age-related Cognitive Decline

Mindfulness-Based Stress Reduction, Health Education and Exercise

MEDEX
Start date: April 2015
Phase: N/A
Study type: Interventional

The purpose of this research is to examine the effects of four interventions on age-related cognitive decline in healthy older adults. The investigators will examine the effects of Mindfulness Based Stress Reduction (MBSR) psychotherapy, multi-component intensity-based aerobic exercise, and their combination, compared to a discussion group.

NCT ID: NCT02416401 Completed - Clinical trials for Age-related Cognitive Decline

Attention Training for Learning Enhancement and Resilience Trial

ALERT
Start date: November 2015
Phase: N/A
Study type: Interventional

Healthy aging is associated with a decline in multiple cognitive domains, as well as motor control function. The long-term consequences of cognitive and functional impairment resulting from age-related cognitive decline are well documented in the scientific and clinical literature, with significant evidence of related problems with independent functional abilities. This study aims to understand how the experimental computer program can affect cognition and attention in participants with age-related cognitive decline.

NCT ID: NCT02228187 Completed - Dementia Clinical Trials

Brain-Computer Interface System for Training Memory and Attention in Elderly

Start date: July 2015
Phase: Phase 2
Study type: Interventional

The primary objective is to examine the efficacy of 8-weeks of a locally developed brain-computer interface based system intervention for improving attention and memory in healthy elderly and those with age related cognitive decline. We hypothesize that elderly who have completed the training program will have significant improvement in their attention and memory compared to the controls, based on the Repeatable Battery for the Assessment of Neuropsychological Status.

NCT ID: NCT02185222 Completed - Memory Disorders Clinical Trials

Effect of Vitamin D on Cognitive Decline of Patients With Memory Complaint

D-COG
Start date: October 23, 2014
Phase: Phase 3
Study type: Interventional

As recommended allowance of oral vitamine D are unable to ensure the recommended serum concentration of vitamine D, the purpose of this study is to show that a dose of vitamin D3 higher than the recommended allowance may slow the cognitive decline of patients with a memory complaint.

NCT ID: NCT02119078 Active, not recruiting - Delirium Clinical Trials

Acute Care for Elders (ACE) Program at OHSU Hospital

Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this investigation is to assess the effectiveness of a multi-disciplinary Acute Care for Elders (ACE) program dedicated to the care of patients age 70 and older admitted to Oregon Health & Science University's hospital medicine service. The ACE program will aim to improve the quality of care of older patients in the investigators hospital by implementing focused interventions and recommendations specific to geriatric needs and syndromes, including: reduced fall rate, decreased incidence and duration of delirium, early recognition and treatment of impaired mobility and function, careful minimization of medication use, prevention of unnecessary catheter and restraint use, decreased hospital readmission rates, improved transitional care following hospital discharge, and high levels of patient and referring physician satisfaction. Additionally, the ACE program aims to improve resident and student competence in treating geriatric syndromes, and to improve staff and learner satisfaction with caring for older adults. ACE programs have been well studied at other institutions, so the investigators will be implementing a program that is already standard of care, and studying the elements that are unique to OHSU. This will be a quality improvement project. Study participants will be a convenience sample of OHSU faculty, staff, residents and students who are employed by or on rotation with General Medicine Team 1 of the Medicine Teaching Service. Faculty, staff, and learners (ACE team members) will receive the ACE training. Study personnel will conduct prospective and retrospective chart review of patients admitted to the ACE service to determine outcomes as noted above.

NCT ID: NCT01953705 Active, not recruiting - Alzheimer's Disease Clinical Trials

n-3 PUFA for Vascular Cognitive Aging

Start date: May 2014
Phase: Phase 2
Study type: Interventional

Brain scans can help identify changes that appear to increase risk for cognitive decline and dementia. Some of these brain changes are thought to reflect actual damage to the small blood vessels that support normal brain function. This clinical trial will determine whether an omega 3 polyunsaturated fatty acid (PUFA) therapy can promote brain health by supporting the small blood vessels in the brain over 3 years in older adults at high risk for cognitive decline and dementia of Alzheimer's type.