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Cognitive Dysfunction clinical trials

View clinical trials related to Cognitive Dysfunction.

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NCT ID: NCT04647032 Completed - Clinical trials for Mild Cognitive Impairment

Enhancing Cognitive Control in Mild Cognitive Impairment Via Non-invasive Brain Stimulation

Start date: January 11, 2021
Phase: N/A
Study type: Interventional

The overall goal of this project is to improve cognitive control abilities in adults with mild cognitive impairment (MCI) through a form of non-invasive brain stimulation, transcranial alternating current stimulation (tACS).

NCT ID: NCT04646499 Completed - Clinical trials for Mild Cognitive Impairment

Feasibility of Gamma Transcranial Alternating Current Stimulation to Reduce Beta-amyloid Load and Improve Memory

Start date: January 18, 2021
Phase: N/A
Study type: Interventional

This project assessed the feasibility of transcranial alternating current stimulation in the gamma band to lower beta-amyloid load and improve memory performance.

NCT ID: NCT04645134 Completed - Aging Clinical Trials

Physical Activity and Cognitive Function in Older Adults: A Novel Role for GPLD1

BrainFit
Start date: April 1, 2021
Phase:
Study type: Observational

The investigators are conducting a cross-sectional, observational study to investigate whether plasma GPLD1 concentrations are associated with higher cognitive function and better brain structure and function in two groups of older adults with high or low levels of physical activity.

NCT ID: NCT04644419 Completed - Clinical trials for Acute Myeloid Leukemia

Chemotherapy-related Cognitive Impairment and Acute Leukemia

Start date: November 3, 2020
Phase:
Study type: Observational

This is an ancillary study of an intervention study (NCT04570709). The parent study is a single institution, feasibility trial of 20 (10 control and 10 intervention) patients with the primary objective of assessing feasibility, acceptability, and change in pre and post measures of symptoms, function, and quality of life by administering the Palliative and Collaborative Care InTervention (PACT). We will further assess cognitive function in the patients who participate in the control of the parent study.

NCT ID: NCT04643327 Recruiting - Parkinson Disease Clinical Trials

Uncovering a Novel Therapeutic Target to Reduce Dementia Risk in Parkinson's Disease

TRIP
Start date: February 9, 2021
Phase: Phase 2
Study type: Interventional

The present study is a proof-of-concept clinical trial to test the efficacy of low doses of a repurposed anti-epileptic drug (levetiracetam) in treating memory problems in Parkinson's disease (PD). Neuroimaging techniques will be used to determine the effect of the drug on specific brain regions (hippocampal subfields). Finally, baseline brain activity of PD patients with memory problems will be compared to PD patients without memory problems and healthy older adults to determine if activity in specific brain regions (hippocampal subfields) can be used to predict memory problems in PD. This information will be useful for future clinical trials to target drugs to these brain regions.

NCT ID: NCT04643132 Recruiting - Postoperative Pain Clinical Trials

S-ketamine Prevents Postoperative Pain and Cognitive Dysfunction After Tibial Fracture

Start date: December 15, 2020
Phase: N/A
Study type: Interventional

Purpose: To explore effects of S-ketamine on postoperative pain and cognitive dysfunction after tibial fracture and orthopedic surgery. To evaluate and examine the incidence of adverse effects with the purpose of selecting the optimum dose.

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: NCT04641663 Enrolling by invitation - Aging Clinical Trials

Multi-target Dietary Supplement Tolerability in an Aging Population (MTDSST)

MTDSST
Start date: September 3, 2021
Phase: N/A
Study type: Interventional

This study is being performed to determine if a multi-ingredient dietary supplement is safe and easy to take by healthy older adults. Participants will be required to take one of three different doses of the dietary supplement for 90 consecutive days and complete wellness surveys and a daily log while taking the supplement. Participants will also provide blood samples at the start of the study, after 30 days, and at the end of the study which will help determine how participants respond to the supplement.

NCT ID: NCT04638608 Completed - Clinical trials for Cognitive Impairment

A Complex Intervention Study on a Palliative Rehabilitation Blended Learning Program to Support Relatives and Health Care Providers of People With ALS and Cognitive Impairments in Coping With Challenges

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

A complex intervention study on a palliative rehabilitation blended learning program to support relatives and health care providers of people with ALS and cognitive impairments in coping with challenges.

NCT ID: NCT04638478 Recruiting - Meningioma Clinical Trials

PREselection of Patients at Risk for COgnitive DEcline After Radiotherapy Using Advanced MRI

Start date: April 8, 2021
Phase:
Study type: Observational

Meningioma are slow growing and frequently occurring intracranial tumors, responsible for 33% of all asymptomatic intracranial tumors and 13-26% of all symptomatic primary brain tumors. The 10-year survival rate is 72%. A variety of treatment options is available for symptomatic meningioma including surgical removal with or without radiotherapy or radiotherapy alone. These therapies can have negative impact on cerebral functioning. After high dose radiotherapy for primary or metastatic brain tumors 50-90% of > 6 months' survivors develop irreversible disabling cognitive decline leading to premature loss of independence, reduced Quality of Life (QOL) as well as significant economic burden both at the individual as societal level. Especially for patients with a good prognosis like benign meningioma, maintaining neurocognitive function is crucial. Understanding the mechanisms underlying radiation induced cognitive decline is complex and which brain areas to spare are an important subject of research. Evaluation methods to assess cognitive function and predict cognitive decline are urgently needed, this will allow the development of optimized treatment strategies with the aim to preserve or even improve cognitive function in meningioma patients. Improvements in the field of neuroimaging techniques (i.e. advanced MRI techniques) have the possibility to identify areas susceptible to cognitive impairment. This allows in the future a more personalized radiation treatment by identifying patients at risk, by optimizing the radiotherapy dose to specific brain regions, that could eventually reduce or prevent, cognitive decline. Improvements in the field of radiotherapy for example by higher precision treatment such proton therapy have potential in obtaining these more individualized strategies.