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Age-Related Cognitive Decline clinical trials

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NCT ID: NCT06226103 Completed - Clinical trials for Age-related Cognitive Decline

Effectiveness Of Computer-Based Cognitive Training in Age-Related Cognitive Decline

Start date: January 7, 2023
Phase: N/A
Study type: Interventional

Background: Ageing is frequently accompanied by physiological changes that might result in a deterioration in physical and cognitive abilities, which frequently leads to institutionalization or the loss of autonomy. Mild cognitive impairment (MCI) is an intermediate state between normal cognitive aging and early dementia, the optimal period to intervene with preventive strategies and early treatments. Thus, the current study intends to investigate the effects of aerobic and computer-based cognitive training on age-related cognitive decline. Methods: This is a single-blinded, randomized controlled trial. Elderly patients with mild cognitive impairment (n = 60) will be randomized to 2 arms and treated for 12 weeks: arm 1 (aerobic exercise and computerized cognitive training) and arm 2 (Placebo; will not receive any intervention). Outcome measure used were Montreal Cognitive Assessment (MOCA) test, Barthel Index (BI) and short form survey-12 (SF-12). Statistical Analysis: To compare the baseline characteristics and outcome variables between the two groups, independent t-tests was employed. A two-way repeated measures ANOVA was utilized to determine the interaction effect of time (baseline, post-treatment, and follow-up) and group (intervention vs. control) on the outcome measures.

NCT ID: NCT05924490 Completed - Clinical trials for Age-related Cognitive Decline

Cognitive Engagement and Aging Mind

Start date: January 31, 2013
Phase: N/A
Study type: Interventional

The purpose of this research is to examine whether and to what extent training of different types of cognitive engagement will improve performance on fluid cognitive abilities that typically decline with age. The research covered by this protocol will use behavioral data that yield response latencies and accuracies of the untrained tasks, and brain activations in fMRI tasks, to test specific hypotheses about neural plasticity and cognitive plasticity from these engagement techniques. Hence, human subjects will be employed in an experiment lasting for 20 hours spanning over 2 months where they will either receive real-time strategy-based videogame training or crystallized intelligence training. In addition, long-term retention data will be obtained after 6 month post-training to investigate any long-term benefits.

NCT ID: NCT05828043 Completed - Clinical trials for Age-related Cognitive Decline

Brain Aging: Muscle-to-brain Axis Modulates Physio-cognitive Decline

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

The primary goal is to develop a multidomain intervention program focused on preserving global or regional brain volume and functions while simultaneously improving physical mobility and cognitive functions in older individuals with mobility frailty. This initiative seeks to unravel the brain-muscle axis mechanisms contributing to the accelerated functional declines observed in older populations. Moreover, our objective includes examining the relationships between the intervention and a broad spectrum of clinical characteristics, phenotypic traits, biochemical profiles, myokines, proteomics, metabolomics, brain imaging, and our previously identified discoveries involving exosomal miRNA.

NCT ID: NCT05693441 Completed - Clinical trials for Age-related Cognitive Decline

Study on the Chronic and Acute Effects of Nordic Berry Beverage on Cognitive Function

SCANBerry
Start date: January 17, 2023
Phase: N/A
Study type: Interventional

The aim of the current study is to investigate whether acute and 12-weeks daily intake of Nordic berries can improve cognitive abilities of adults without cognitive disease, and whether the effect can be linked to changes in metabolic parameters.

NCT ID: NCT05602220 Completed - Alzheimer Disease Clinical Trials

Heartrate and Breathing Effects on Attention and Memory 1

HeartBEAM
Start date: January 11, 2023
Phase: N/A
Study type: Interventional

In the current study, we will examine how daily paced breathing affects plasma amyloid beta levels and the rate of learning in older adults. Healthy adults aged 50-70 who meet all eligibility criteria will be invited to this study. Participants will be randomly assigned to one of the two conditions: 1) Daily memory and attention training followed by a paced breathing protocol designed to increase relaxation or 2) Daily memory and attention training followed by a paced breathing protocol to increase alertness. Participants will be asked to complete pre and post intervention cognitive testing online, engage in 10 weeks of daily brain training (starting Week 2) and 9 weeks of paced breathing (starting Week 3) at home. They will also be asked to come in for lab visits on Weeks 2, 7 and 12 to provide blood and urine samples to assess amyloid beta levels and to complete magnetic resonance imaging scans to assess perivascular space volume.

NCT ID: NCT04938778 Completed - Clinical trials for Age-related Cognitive Decline

Think FAST Research Study

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

To test a 14-hour prolonged nightly fasting (PNF) protocol in a group of older adults (≥ 65 years old) with self-identified age-related cognitive decline (ARCD) on the primary outcome of neurocognitive function and performance as measured by objective outcomes. The investigators will use an 8-week single group pre-post pilot study design to measure outcomes related to neurocognitive function and performance and cardiometabolic risk factors (i.e., sleep disturbances, body mass index).

NCT ID: NCT04910399 Completed - Memory Impairment Clinical Trials

Development of an Innovative Health Ingredient From Marine By-products for the Healthy Aging

BRAINBOOSTER
Start date: September 14, 2021
Phase: N/A
Study type: Interventional

This interventional, randomised, placebo-controlled and double-blind study aims to evaluate the effect of a dietary supplementation with a blue fish hydrolysate derived from marine by-products, containing peptides and n-3 polyunsaturated fatty acids, on cognitive performance in a healthy older population, between 60 and 73 years old, with lower memory performance.

NCT ID: NCT04568057 Completed - Clinical trials for Age-related Cognitive Decline

Effect of Transcranial NIR Light Upon Memory

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

A double-blind placebo-controlled study evaluating the effect of 1068nm NIR trans-cranial phototherapy upon the cognitive function of healthy individuals between the age of 45 years and 80 years.

NCT ID: NCT04195230 Completed - Clinical trials for Age-related Cognitive Decline

Cognitive Multi-Tasking Training in Healthy Older Adults

Start date: January 2, 2020
Phase: N/A
Study type: Interventional

This study evaluated the feasibility of a remote web-based ecological cognitive training protocol to healthy older adults. The training protocol involves 5 training sessions.

NCT ID: NCT03771131 Completed - Clinical trials for Age-related Cognitive Decline

A Group Study on the Effects of a Short Multi-Domain Cognitive Training in Healthy Elderly Italian People

Start date: December 1, 2013
Phase: N/A
Study type: Interventional

Alongside physiological cognitive ageing, nowadays there is an alarming increase in the incidence of dementia that requires communities to invest in its prevention. The engagement in cognitively stimulating activities and strong social networks have been identified among those protective factors promoting successful cognitive ageing. One aspect regarding cognitive stimulation concerns the relevance of the frequency of an external intervention. For these reasons, the aim of this study was to evaluate the efficacy of a 3-month multi-domain cognitive training program, administered once per week in a group of healthy elderly aged over 60 years old. Their results obtained on a series of neuropsychological tests, both pre- (t0) and post-training (t1), were compared with those of a passive control group who did not receive the cognitive training.