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Cognitive Change clinical trials

View clinical trials related to Cognitive Change.

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NCT ID: NCT03864536 Completed - Health Behavior Clinical Trials

A Multidomain Approach to Preventing Dementia in African Americans: Cognitive Prescriptions

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

The goal of this R21 study is to explore the feasibility and preliminary efficacy of individualized cognitive prescriptions (CogRxs) in improving engagement in healthy behaviors and other outcomes in middle-aged AAs and to gain feedback on future implementation of the program.

NCT ID: NCT03813888 Completed - Cognitive Change Clinical Trials

Effect of Arshvidya After School Program on Cognitive Processes in Elementary School Children

Start date: March 21, 2017
Phase: N/A
Study type: Interventional

The impact of Arsha Vidya program on cognitive performance was examined in elementary school children. The study compares the effects of arsha vidya after school routine with usual after school routine in healthy 8-11 year-old Indian children. The main objective of the study is to investigate the effect on cognitive function, behaviour and emotions.

NCT ID: NCT03805685 Completed - Cognitive Change Clinical Trials

Preoperative Risk Factors and Perioperative Neurocognitive Disorders

Start date: February 3, 2019
Phase:
Study type: Observational

Perioperative neurocognitive disorders (PND's) remain an important complication after surgery. After many years of speculating about the etiology of this complication, currently studies are pointing to an inflammatory cascade being set in motion. This prospective study is designed to examine preoperative lifestyle factors (such as sedentary behavior) associated with postoperative cognitive impairment in a group of patients undergoing non-cardiac surgery. The objectives in our study are to: identify perioperative risk factors for the development of PND's measure the incidence and duration of perioperative neurocognitive disorders in a known high-risk group of elective surgical patients measure a peripheral inflammatory marker (interleukin 6: IL-6) in the same group of surgical patients

NCT ID: NCT03768557 Completed - Cognitive Change Clinical Trials

The Effect of Acute Minocycline Administration on Emotional Processing and Cognition in Healthy Volunteers

Start date: April 26, 2017
Phase: N/A
Study type: Interventional

There is growing interest in the possibility of producing more effective antidepressant treatments that target a wider range of pathways involved in depression, including anti-inflammatory and anti-glutamatergic systems. Minocycline is a novel pharmacological agent; in addition to its antibiotic and anti-inflammatory properties, it also acts in the brain as an anti-glutamatergic and anti-oxidant agent. Since both excessive glutamate and oxidative stress are implicated in major depression, and appear to be connected to pro-inflammatory activity, this drug offers a unique tool with which the investigators can measure the effects of targeting these pathways on emotional processing. Participants will receive a single dose of either the drug (200 mg minocycline) or placebo, and will then undergo a well-validated computerised battery of emotional processing tasks that have previously been shown to be sensitive to standard antidepressant drugs. Tasks include presentation of positive and negative emotional words or pictures, to which participants' responses are measured. These tasks have been widely used previously without any adverse effects.

NCT ID: NCT03740152 Completed - Cognitive Change Clinical Trials

Transcranial Near-Infrared Light in Healthy Subjects: a Cerebral Blood Flow Study With Diffuse Correlation Spectroscopy

NIR-Flow
Start date: August 22, 2017
Phase: N/A
Study type: Interventional

Transcranial Light Therapy involves non-invasive and invisible beams of light that increase energy metabolism in the brain. Transcranial light therapy has been found to promote brain metabolism. The purpose of the study is: To asses the change in cerebral blood flow induced by the Transcranial Continuous and Pulse Near-Infrared Light Therapy in healthy subjects. To correlate with cognitive performance the change in cerebral blood flow induced by the Transcranial Continuous and Pulse Near-Infrared Light Therapy in healthy subjects. To correlate with skin pigmentation the change in cerebral blood flow induced by the Transcranial Continuous and Pulse Near-Infrared Light Therapy in healthy subjects. To assess the safety and tolerability of the Transcranial Continuous and Pulse Near-Infrared Light Therapy in healthy subjects

NCT ID: NCT03737552 Completed - ADHD Clinical Trials

Sleep Patterns in Children and Adolescents With ADHD

Start date: April 23, 2019
Phase:
Study type: Observational

This study is aimed to find out Sleep profile differences in children and adolescents with and without ADHD,Relationship between sleep profile disturbance and ADHD symptoms, Impact of sleep disturbance on cognition functions and quality of life.

NCT ID: NCT03695003 Completed - Cognitive Change Clinical Trials

Cognitive Effects of Sage in Healthy Humans

Start date: September 3, 2018
Phase: N/A
Study type: Interventional

Extracts of sage and polyphenols have separately been reported to interact with central nervous system (CNS) mechanisms relevant to cognitive performance but, to date, no trial has combined these interventions. The current study investigates the effects of this combined intervention in N=90 healthy males and females between 30-60 yrs, at 600 mg versus placebo, on cognition and mood over a 29 day period.

NCT ID: NCT03689348 Completed - Clinical trials for Stress, Psychological

Acute and Chronic Effects of Avena Sativa on Cognition and Stress

Start date: September 24, 2018
Phase: N/A
Study type: Interventional

The flavanoid and terpene phytochemicals present in wild green oat interact with multiple mechanisms relevant to brain function; including those which would modulate cognition and stress. The current study aims to test this in a group of N=128 males and females between the ages of 35-65yrs before and after 28 days supplementation of placebo, 300-, 600- and 900mg of a wild green oat extract.

NCT ID: NCT03674281 Completed - Clinical trials for Type 1 Diabetes Mellitus

The VRIF Trial: Hypoglycemia Reduction With Automated-Insulin Delivery System

Start date: September 24, 2018
Phase: N/A
Study type: Interventional

The objective of this pilot study is (i) to test the use of an Artificial Pancreas (AP) System as a viable therapy treatment for two vulnerable populations: 6 to 10 year-old and adults older ≥65 years old with T1D; (ii) to assess cognitive function in children and older adult patients with T1D and examine whether improved glycemic control defined by stable (more than 70% of the day in glycemic range 70-180 mg/dL) control positively influences cognitive function; and (iii) obtain preliminary data to apply to funds to continue with larger and longer clinical trials.

NCT ID: NCT03673930 Completed - Cognitive Change Clinical Trials

Cognitive and Cerebral Blood Flow Effects of Zanthozylum Armatum Fruit Extract in Healthy Adults Aged 30 - 55

Start date: April 6, 2018
Phase: N/A
Study type: Interventional

Zanthozylum armatum (Z. armatum)—otherwise known as Nepalese pepper, or timut—is an perennial shrub found in India and across Southeast Asia. Preparations of the bark, fruit and seeds of Z. armatum have been extensively used in traditional Indian medicine. Preliminary data have indicated that preparations of Z. armatum may also be beneficial to cognitive function. The study aims to investigate the effects acute and chronic consumption of Z. armatum on cognitive function and cerebral blood flow.