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Cognitive Change clinical trials

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NCT ID: NCT05906654 Completed - Cognitive Change Clinical Trials

Sharing History Through Active Reminiscence and Photo-imagery (SHARP) Pilot Program

SHARP
Start date: February 5, 2016
Phase: Early Phase 1
Study type: Interventional

SHARP is a neighborhood-based and technology-supported approach to brain health for older Black adults that integrates walking and image-prompted social reminiscence to maintain or improve brain health.

NCT ID: NCT05905081 Completed - Cognitive Change Clinical Trials

Acute Effects of Moderate Intensity Aerobic Exercise on Cognitive Functions in Young Adult Males

Start date: June 20, 2023
Phase: N/A
Study type: Interventional

60 healthy male university students will be included in this study. Physical fitness parameters, fluid intelligence, and physical activity level will be measured at baseline. Participants will be randomised to one of two testing schedules, groups will complete either a 30-minutes aerobic exercise session or a resting control condition. Cognitive measures (simple reaction time task, go/nogo task, spatial cueing, n-back task) will be tested before and after the intervention.

NCT ID: NCT05894967 Recruiting - Cognitive Change Clinical Trials

Moderators and Mediators of Perceptual Learning

Start date: April 14, 2023
Phase: N/A
Study type: Interventional

This study addresses the fundamental issue of specificity and generality of training in the context of Perceptual Learning (PL). PL broadly encompasses the set of mechanisms through which experience with the environment gives rise to changes in perceptual processing. Careful research in this domain can greatly enhance our basic understanding of the perceptual systems and the plasticity of these systems. Furthermore, translational approaches underpinned by the basic science of PL are becoming increasingly prominent. This includes a host of emerging translational approaches for the rehabilitation of both perceptual deficits and for cognitive training, which are believed to share cortical plasticity mechanisms. However, while existing research provides evidence that PL approaches can improve perceptual skills, our ability to develop effective interventions is limited by a lack of understanding of the behavioral outcomes associated with different PL approaches. One major obstacle to successful translation of PL is that the field to-date has been strongly driven by "novel" and "provocative" findings demonstrated via small N studies with very few projects digging deep to achieve robust and reliable results. In turn, not surprisingly, the field of PL, like many others in psychology, has suffered from numerous replication challenges. Here we address these limitations by comparing a large number of different training tasks using common outcome measures and in a large subject population. Each training tasks involves a different "critical feature" for learning proposed by one or more research groups. However, these training tasks have never been directly compared or contrasted. Robust and reliable results will be achieved by training a large sample of participants on PL tasks and assess the outcomes via a common set of measures. The investigators will also collect a broad assessment of individual differences, which will provide a unique dataset that can resolve controversies in the literature and lead to new understandings. Our proposed analytical approach tests several key hypotheses in the field, explores the extent to which different training approaches lead to systematically different profiles of learning, and examines how these can differ based upon the individuals being trained.

NCT ID: NCT05879562 Active, not recruiting - Clinical trials for Cognitive Impairment

Validation of a Digital Self-Administered Cognitive Screening Tool: MoCA-XpressO

MoCA
Start date: October 1, 2022
Phase: N/A
Study type: Interventional

The investigators conducted a validation study for the Montreal Cognitive Assessment (MoCA)-XpressO compared to the digital-MoCA test (version 8.1) as the gold standard. Participants were recruited from the MoCA clinic and a family practice. Ethics approval was received, and all participants provided informed consent. A crossover study design was applied to the MoCA-XpressO and the digital-MoCA test; participants were randomized for the order of administration. The investigators only recruited participants who did not complete a MoCA test during the 3 months prior to the study. A logistic regression model was built, and the accuracy of the model was evaluated by the sensitivity, specificity, and area under the Receiver Operating Characteristic (ROC) curve.

NCT ID: NCT05868798 Completed - Sleep Clinical Trials

Can Ammonium Inhalants Maintain Performance in Sleep Deprived Soldiers?

Start date: October 1, 2020
Phase: Phase 1
Study type: Interventional

This study aims to examine the effectiveness of ammonia inhalants in countering the effects of total sleep deprivation on cognitive and physical performance tests relevant to military personnel.

NCT ID: NCT05855434 Recruiting - Clinical trials for SARS-CoV-2 Infection

The ACDC Study Assessing Cognitive Deterioration in COVID-19

ACDC
Start date: February 1, 2023
Phase:
Study type: Observational

The long-term impact and effects of COVID-19 are still being determined. However, what is clear, is that some people are still struggling following a period of illness with COVID-19. Now known as 'long covid' or 'post covid-19 syndrome', people are not only experiencing physical symptoms like fatigue and breathlessness, but also psychological difficulties, as well as cognitive changes often referred to as 'brain fog'. This can include symptoms, such as changes in memory, difficulties with organisation and problem solving, as well as the ability to concentrate. Evidence from other research areas suggest that these changes could be due to shrinkage in areas of the brain that control functions like memory and concentration. There are also connections between different brain areas that work together to perform tasks such as remembering and concentrating, and these areas may also be affected by COVID-19. The purpose of this study is to scan the brains of patients reporting cognitive changes having been hospitalised with COVID-19 infection to see if any of these areas or connections have changed after infection and whether this might explain these cognitive changes.

NCT ID: NCT05841173 Recruiting - Obesity Clinical Trials

Effects of Weight Loss Management on Cognitive Function in Elderly Women With Obesity

Start date: January 9, 2022
Phase: N/A
Study type: Interventional

According to studies, the risk of cerebrovascular disease and cognitive decline are associated with age-related changes. In addition, there is data suggesting a relationship between the progression of this pathology and the presence of obesity and associated metabolic disorders. According to to some research, weight loss associated with cognitive function decline. In this regard, the development of effective, applicable in real clinical practice methods of non-drug treatment and prevention of cerebrovascular disorders and age-related cognitive decline in people with obesity and metabolic disorders, who are at high risk, seems to be extremely relevant. The main goal of the study is to compare the effectiveness of various weight loss approaches and to study their effects on the cognitive functions of elderly obesity women.

NCT ID: NCT05782348 Recruiting - Gingivitis Clinical Trials

Evaluating the Effectiveness of a Cognitive Behavioral Intervention (CBI)

Start date: February 6, 2023
Phase: N/A
Study type: Interventional

This is a Phase III, randomized, one-center, three arm parallel group, open label and single blind clinical study to evaluate the effectiveness of a cognitive behavioral intervention (CBI) adjunctive to a smart powered toothbrush on the oral health of adolescents.

NCT ID: NCT05735353 Completed - Cognitive Decline Clinical Trials

Sleep, Diet, Exercise and Older Persons

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

To examine the impacts of a cognitive yoga program and circuit resistance training on cognitive and physical performance with nutrition and sleep as modulating factors in healthy, older adults.

NCT ID: NCT05715073 Completed - Cognitive Change Clinical Trials

Improving Cognition With Neurodegradation Countermeasure

Start date: March 1, 2023
Phase: N/A
Study type: Interventional

The goal of this randomized, placebo-controlled, three-condition, double-blind, within-participants crossover clinical trial is to compare caffeine, TeaCrine plus caffeine, and a placebo condition in ROTC or tactical personnel. The main question it aims to answer is the effect of the condition on measures of cognitive performance, cardio-autonomic, and hemodynamic responses after a physically demanding protocol. The physiological function will be derived from metrics of heart rate variability, whilst cogntive performance will be evaluated using tasks that assess cognitive domains of executive function, reaction time, and memory. Participants will report to the lab 4 times, once for familiarization of cognitive measures and then 3 times for their experimental visits. Participants will consume their randomized condition an hour prior to the fatiguing interval exercise protocol. Following they will complete a series of cognitive tasks.