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Cognitive Change clinical trials

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NCT ID: NCT04860050 Completed - Stress Clinical Trials

Turmeric for Memory Impairment and Cognition

TURMEMIC
Start date: April 19, 2021
Phase: N/A
Study type: Interventional

The objective of the study is to test the capacity of acute and chronic supplementations of Turmipure GOLD® to improve cognitive performance in healthy aging

NCT ID: NCT04823338 Completed - Child Development Clinical Trials

Conectar Jugando Online: Board Games to Improve Executive Function in School-age Children (CJ-Online)

CJ-Online
Start date: December 16, 2020
Phase: N/A
Study type: Interventional

Good development of executive functions at school has been related to a better adaptation of children in different areas of their daily life and, especially, with adequate academic performance. Taking into account the importance of play in childhood, some interventions aimed at training these cognitive processes have been based on the use of playful elements, such as modern board games. Although it is still an unexplored field of research, some studies with older elementary school children and with ADHD children have found significant improvements in executive functions after training that had the board game as a key intervention element. However, we still do not have studies that have explored the possible cognitive benefits of its use throughout the primary stage with the general population. For this reason, the main objective of this study is to test the effectiveness of a cognitive training program based on modern board games in primary education children (6 to 12 years old).

NCT ID: NCT04790188 Completed - Cognitive Change Clinical Trials

Effect of a Nootropic on the Cognitive Performance in Young Adults

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

The main aim of this study is to determine the effect of a nootropic on cognitive performance (i.e., reaction time, inhibitory control, cognitive flexibility, working memory, neuro-psychological outcomes).

NCT ID: NCT04749264 Completed - Mental Health Issue Clinical Trials

The Influence of Mindfulness Meditation Retreat on Attention to Internal Experience

Start date: August 1, 2020
Phase:
Study type: Observational

Although attention is thought to have a definitive functional role in mindfulness meditation training and its salutary mechanisms of action, extant empirical evidence is mixed and limited. In the proposed study, we propose to test whether 6 to 7-days mindfulness meditation retreats (N=90), relative to a wait-list control condition (N=45), will impact internal attentional processes or attention to internal experience (e.g., thoughts and bodily sensations); and whether these internal attentional change processes predict salutary outcomes of mindfulness meditation retreats. Participants will complete tasks designed to measure attention to internal experience before and then immediately following the retreat, as well as self-report measures of salutary outcomes before and 2-weeks post-retreat. Matched controls will complete the tasks at parallel time-points in the lab.

NCT ID: NCT04703296 Completed - Cognitive Change Clinical Trials

Mindfulness Training in Special Operations Forces (SOF) Candidates

Start date: March 16, 2022
Phase: N/A
Study type: Interventional

The overarching goal of this study is to develop, deliver, and investigate the utility and feasibility of train-the-trainer delivery of mindfulness training (MT) in support of improved readiness (across cognitive, affective, and social domains of the human dimension) and improve retention of candidates in the SOF qualification pipeline at the U.S. Army John F. Kennedy Special Warfare Center and School (referred to as SWCS).

NCT ID: NCT04654936 Completed - Cognitive Change Clinical Trials

Effectiveness of a 12 Week Theory Driven Intervention Promoting Adherence to the MIND Diet

Start date: May 16, 2019
Phase: N/A
Study type: Interventional

This study aims to test the feasibility and acceptability of a 12 week online dietary promoting MIND diet behaviour. This study also tests the effectiveness of the MIND diet on cognitive function, mood, quality of life and participants capability, opportunity and motivation towards adoption of the MIND diet.

NCT ID: NCT04651582 Completed - Dementia Clinical Trials

The Everyday Function Intervention Trial

EFIT
Start date: January 5, 2021
Phase: N/A
Study type: Interventional

Loss of independence, cognitive decline, and difficulties in everyday function are areas of great concern for older adults and their families. From a public health perspective, successful efforts that enable older adults to age within their homes, as compared to nursing homes, will save an estimated $80 billion dollars per year. Cognitive training is one intervention that maintains cognition, everyday function, and health. Although clearly an important and effective intervention, the mediators, or mechanisms, underlying this program are unknown. Our overall objective is to assess the cognitive and psychosocial factors within daily life that account for the transfer of one form of cognitive training to everyday function. This exploratory double-blind trial will randomize older adults to 20 hours of cognitive training or cognitively stimulating activities. The investigators will assess cognitive and psychosocial factors before, during, and after training within daily life. The investigators will then compare such factors and assess how they impact the transfer of cognitive training to everyday functioning. The investigators will also include an eligible sub group of the EFIT participants who will have functional MRI brain scans and sleep evaluation using the Sleep Profiler, a clinically approved device, at pre and post brain training. The investigators will also monitor daily activity in this sub group using FitBIt watches. Our central hypothesis is that improvements in daily processing speed and attention, key components of higher order cognitive functions, will have the strongest relationship with everyday function changes. This exploratory study is the first of its kind and will be used to provide important data relevant to a future larger randomized controlled trial examining mediators of cognitive training in a representative sample of adults. Additionally, all data collection, with the exception of MRI, can be completed remotely within the participant's home. This information will assist in the future development of more effective home- and community-based interventions that maintain everyday function.

NCT ID: NCT04648670 Completed - Aging Clinical Trials

Cognitive Stimulation Program in Elderly

Start date: December 1, 2011
Phase: N/A
Study type: Interventional

The participants who carry out our cognitive stimulation program maintain and / or improve their score of the 35-point Spanish version of 35 points of Mini-mental State of Folstein; Mini-exam Cognoscitive of Lobo

NCT ID: NCT04643080 Completed - Inflammation Clinical Trials

Dairy Based Probiotic Intervention and Cognitive, Emotional, and Inflammatory Outcomes

Start date: March 7, 2019
Phase: N/A
Study type: Interventional

The purpose of this study was to determine the effect of dairy-based probiotics on cognitive function, emotional wellbeing, and inflammation. Subjects were assigned to either consume 6 oz of yogurt/day or abstain from consuming yogurt and other probiotic-containing foods for 12 weeks. Subjects completed baseline testing and 12-week follow-up testing consisting of a laboratory blood draw to assess inflammatory biomarkers, and a computerized assessment to evaluate cognitive and emotional wellbeing measures.

NCT ID: NCT04598386 Completed - Cognitive Change Clinical Trials

The Effect of AMP Human Sodium Bicarbonate Lotion on Hydration

AMPlify
Start date: December 9, 2020
Phase: N/A
Study type: Interventional

The purpose of this research study is to evaluate the effects of a topical sodium bicarbonate lotion on physiological and psychological responses associated with hydration status and fluid balance in humans during passive heat stress. Currently, the ingestion of sodium has been an effective measure for improvements in fluid regulation and hydration status in humans. However, the investigators do not know its regulatory relationship with measurements of fluid balance when supplemented through the skin.