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Cognitive Change clinical trials

View clinical trials related to Cognitive Change.

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NCT ID: NCT06062186 Completed - Cognitive Change Clinical Trials

Acute Effects of Naturally Occurring Tea and Coffee-based Ingredients on Cognitive Performance

Start date: April 5, 2023
Phase: N/A
Study type: Interventional

This study is a double-blind, randomized, three-arm, single-dose, placebo-controlled crossover trial of forty (40) apparently healthy male and female participants. The objective of this study is to assess the effects of AmaTea Max Organic Guayusa Extract and Lion's Mane on cognitive responses including mental clarity, mood, focus, concentration, productivity, anxiety/stress, happiness, and accuracy.

NCT ID: NCT05988593 Completed - Cognitive Change Clinical Trials

Testing the Cognitive Facilitation Effect by Dietary Supplementation of MelaGene+ Drink

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

To assess the efficacy of MelaGene+ on cognitive performance

NCT ID: NCT05925582 Completed - Cognitive Change Clinical Trials

Vestibular-Based Exercises vs. Calisthenic Exercises for Cognitive Functions

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

This study was planned to determine the effects of vestibular-based exercises (VBE) and calisthenic-based exercises (CBE) on the cognitive functions of the older individuals. A total of 30 people (21 male, 9 female; range: 65 - 85) will participate in the study. In this randomized controlled study, 30 participants will be divided into two groups: VBE Group (n: 15) and CBE Group (n: 15). Standardized Mini Mental State Test (SMMT) and 3 dual task (motor + cognitive: Dual Task 1, 2, 3) tests will be used to evaluate the cognitive functions of the participants.

NCT ID: NCT05922137 Not yet recruiting - Dementia Clinical Trials

Oriental Intervention for Enhanced Neurocognitive Health (ORIENT) Diet in Patients With Intracranial / Carotid Stenosis

ORIENT
Start date: July 12, 2023
Phase: N/A
Study type: Interventional

To test the effects of 6 month additional intervention of ORIENT diet versus usual medical treatment for Intracranial / Carotid Stenosis on cognitive decline, multi-mode MRI image markers and serum and fecal biomarkers in a randomized controlled trial of 120 patients with intracranial / carotid stenosis, who are aged older than 40 years and without dementia.

NCT ID: NCT05921084 Active, not recruiting - Stroke Clinical Trials

MIND Diet to Improve Cognitive Function in Mild Stroke Patients

MINDICOMS
Start date: July 23, 2023
Phase: N/A
Study type: Interventional

A 6-month pilot randomized controlled trial designed to test the effect of the Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) Diet + usual medical care versus usual medical care on the rate of cognitive change and several other secondary outcomes through a randomized controlled trial in 60 mild stroke patients aged 35-70 years without dementia.

NCT ID: NCT05919251 Recruiting - Stroke Clinical Trials

Influence of Cognition on Activity and Participation in People With Stroke

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

If a subject agrees to participate, the primary investigators will collect some basic information including age, height, and weight. Intake of some general questions regarding health will be performed and each subject will complete some tests that measure walking speed, cognition, and balance. During these tests participants will be asked to stand from a chair, walk up & down a staircase, walk over objects in a forward, backward, and sideways directions, walk around objects in forward and backward directions. After completing those tests, participants will be asked to repeat them while doing another task such as counting out loud, naming objects, or passing an object from one hand to another.

NCT ID: NCT05912530 Recruiting - Cognitive Change Clinical Trials

The Influence of Gender on Dual Task Performance in Young Healthy Adults

Start date: June 30, 2023
Phase:
Study type: Observational [Patient Registry]

Dual tasking (DT), or the act of conducting multiple, simultaneous tasks, is wide spread in daily life .In particular, the vast majority of mobility tasks we complete (e.g., standing, walking, stepping, etc.) occur while distracted by another motor and/or cognitive task. A common feature of DT is that performance on one or both tasks is diminished when completed together .Understanding the relationship between gender and dual task performance is important because this knowledge could help inform us the development of interventions or training programs that target these differences and improve overall performance. Aims: To investigate the gender-related differences in single task performance through motor torque, cognitive tasks and walking speed, and the combined dual-task costs considering both motor and cognitive performance in a sample of young adults

NCT ID: NCT05906667 Completed - Cognitive Change Clinical Trials

Sharing History Through Active Reminiscence and Photo-imagery - With MCI

SHARP-MCI
Start date: May 24, 2017
Phase: Early Phase 1
Study type: Interventional

The SHARP-MCI study tests impact of walking and social reminiscence on cognitive function, blood pressure, and weight among healthy Black Americans and those experiencing mild cognitive impairment (MCI).

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.