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Cognitive Dysfunction clinical trials

View clinical trials related to Cognitive Dysfunction.

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NCT ID: NCT03220295 Completed - Clinical trials for Cognitive Impairment

Putative Cognitive Enhancer VU319

Start date: July 28, 2017
Phase: Phase 1
Study type: Interventional

This is a safety study of the molecule VU319 to ascertain pharmacokinetic and pharmacodynamic data and test cognitive enhancement in healthy volunteers.

NCT ID: NCT03207048 Completed - Bipolar Disorder Clinical Trials

A Study of Repetitive Transcranial Magnetic Stimulation in Bipolar Patients

Start date: July 10, 2017
Phase: N/A
Study type: Interventional

This study will investigate the effect of Repetitive transcranial magnetic stimulation (rTMS) on cognition and long-term clinical outcomes of bipolar patients.

NCT ID: NCT03197454 Completed - Clinical trials for Age-related Cognitive Decline

Brain Enhancement Training Towards Elders Resilience to Aging

BETTER Aging
Start date: June 1, 2018
Phase: N/A
Study type: Interventional

This study is a parallel arm, double-blind, randomized, controlled clinical trial to assess the efficacy of an experimental software program designed to improve cognitive functions versus a computer-based software control. Both the study and the software being investigated meet the criteria of Non-Significant Risk.

NCT ID: NCT03196037 Completed - Clinical trials for Cognitive Impairment

Feasibility of an 8-week Tai Chi Chuan Intervention for Breast Cancer Survivors

Start date: December 5, 2017
Phase: N/A
Study type: Interventional

Purpose:To gather preliminary data and to determine the feasibility and acceptability of an 8-week Tai Chi intervention for adults cancer survivors (survivors) who report experiencing cognitive impairment, and to perform exploratory analyses to assess improvements in cognitive performance, health-related quality of life, brain activity, and blood-based biomarkers. Participants: Adult survivors (> 18 years old) who report experiencing cognitive impairment and are within 60 months of completion of chemotherapy for treatment of a breast cancer diagnosis. Procedures (methods): A single arm pre-/post-test non-randomized study design in adult cancer survivors (Enrollment goal N=15; current age ≥ 18 years, treatment completed within 60 months). Outcomes will be assessed at baseline and after the 8-week Tai Chi intervention, and consist of feasibility, acceptability, expectancy/credibility, health-related quality of life, cognitive performance, serum biomarkers, and brain activity.

NCT ID: NCT03191968 Completed - Quality of Life Clinical Trials

Prostate Cancer Survivors and Exercise and Behavioral Counseling

BOOST
Start date: July 6, 2017
Phase: Phase 2
Study type: Interventional

This study will evaluate the feasibility of delivering a supervised physical activity program plus standard exercise counseling (SPA+EC) versus a supervised physical activity plus motivationally-enhanced behavioral counseling (SPA+BC) in prostate cancer survivors (PCS). Fifty participants (n=25) will be randomized to receiving SPA+EC or SPA+BC (n=25). We hypothesize that PCS receiving the SPA+BC intervention will result in greater increases in objectively-assessed physical activity compared with PCS receiving the SPA+EC intervention.

NCT ID: NCT03187353 Completed - Clinical trials for Cognitive Impairment

IMProving Executive Function Study

IMPRES
Start date: September 22, 2017
Phase: Phase 4
Study type: Interventional

This is a double-blind, placebo-controlled, crossover study testing whether Vyvanse (lisdexamfetamine; LDX) improves executive functioning (EF) in 100 postmenopausal women who report onset of EF difficulties after oophorectomy. This study involves magnetic resonance imaging (MRI) to see how LDX affects brain chemistry while undergoing two 6-week trials of the study drug and placebo capsules. UPDATE: We have recently updated this protocol (09/2020) to offer a remote version of the study that can be completed entirely from the participant's home. This alternate version of the study eliminates travel, the MRI, and blood draws.

NCT ID: NCT03186846 Completed - Cognitive Decline Clinical Trials

Volume Optimisation and Cognitive Function in Major Abdominal Surgery

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

In the last 25 years, there has been a lot of attention directed on reducing perioperative morbidity and mortality by improving intraoperative monitoring and hemodynamic optimisation of patients. Advanced monitoring devices and new parameters have shifted the focus of anaesthesia management from macro- to micro circulation with the emphasis on the determinants of oxygen delivery and tissue oxygenation. There is increasing evidence that long-term outcome is improved by goal-directed optimisation of hemodynamic parameters (optimisation of stroke volume and cardiac output by fluids and inotropic and vasoactive drugs). Besides, new monitoring possibilities (depth of anaesthesia and cerebral and tissue oxygenation monitors) and adherence to protocols have proved beneficial in reducing morbidity cognitive dysfunction. However, questions are raised what the optimal goals (healthy population derived normal values, preoperative values, maximal values, restrictive fluid management) should be. Secondly, all new methods were used separately and there is a lack of studies to show the effect of combined (multimodal) monitoring on occurrence of cognitive dysfunction. All gathered data indicate that the combined use of new methods with adherence to an appropriate protocol might radically improve the perioperative management and outcome of high-risk surgical patients. The present study tests the hypothesis that intraoperative multimodal monitoring with hemodynamic optimisation, BIS-guided anaesthesia and maintenance of optimal cerebral oxygen saturation will reduce cognitive dysfunction.

NCT ID: NCT03186638 Completed - Clinical trials for Cognitive Impairment

Low-Dose Ibuprofen in Improving Cognitive Impairment in Patients With Cancer

Start date: May 26, 2017
Phase: Phase 2
Study type: Interventional

This randomized phase II trial studies how well low-dose ibuprofen in improving cognitive impairment in patients with cancer. Anti-inflammatory agents, such as ibuprofen, may slow the decline of cognitive processes and diseases involving the brain.

NCT ID: NCT03175276 Completed - Cognitive Decline Clinical Trials

Informant Questionaire on Cognitive Decline in the Elderly (IQCODE) and Delirium in Geriatric Patients

Delirium
Start date: March 20, 2017
Phase:
Study type: Observational

To investigate the usefulness of the Informant Questionaire on Cognitive Decline in the Elderly (IQCODE) to predict delirium in elderly patients admitted to Emergency Department (ED) with geriatric assessment and transferred to Geriatric ward.

NCT ID: NCT03166098 Completed - Schizophrenia Clinical Trials

The Role of Dysmyelination in Cognitive Impairment of Psychotic Spectrum Disorders

Start date: July 5, 2016
Phase:
Study type: Observational

This is a single center study that uses both between-group comparisons and correlational analyses to establish biomarkers of dysmyelination and cognitive impairment in Psychotic Spectrum Disorders using imaging and neuropsychological assays.The study will provide non-invasive biomarkers of cognitive dysfunction in Psychotic Spectrum Disorder.