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Cognitive Dysfunction clinical trials

View clinical trials related to Cognitive Dysfunction.

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NCT ID: NCT03805880 Completed - Clinical trials for Cognitive Dysfunction

Cerebral Desaturation and Postoperative Dysfunction After Thoracic Surgery

Start date: January 1, 2018
Phase:
Study type: Observational

The purpose of this study prospective observational study is to determine cognitive dysfunction incidence after thoracic surgery. We also evaluate evaluate the role of cerebral oxygen desaturations and hypertension as risk factors for post-operative cognitive dysfunction (POCD) in patients undergoing lung resection.

NCT ID: NCT03805620 Completed - Clinical trials for Mild Cognitive Impairment

Effects of Combined Physical-cognitive Training on Cognitive Function in MCI

Start date: March 18, 2019
Phase: N/A
Study type: Interventional

The present study aims to investigate the effects of combined physical-cognitive training on cognitive function as well as peripheral BDNF level and mitochondrial function of individuals with MCI. It is hypothesized that: 1) the combined physical-cognitive training program will be superior to the physical and cognitive training program alone; and 2) the degree of cognitive improvement will be positively correlated with the improvement of plasma BDNF and mitochondrial function.

NCT ID: NCT03804840 Completed - Clinical trials for Measuring THC-induced Cognitive Impairment Using a Mobile Application

Developing a Mobile Method to Measure THC-induced Impairment

AIS
Start date: March 1, 2017
Phase: Early Phase 1
Study type: Interventional

Marijuana use, for both recreational and therapeutic purposes, is becoming increasingly common as states remove restrictions on use. The increased use raises new concern about the safety of this drug, including its ability to impair basic cognitive and psychomotor tasks, and whether the users are aware of their impairment. We propose to design a simple performance test that users can use in the field, using a cell phone, to assess their level of impairment relative to their own drug-free state. In this preliminary study, we will compare participants' simple task performance after a known dose of delta-9-tetrahydrocannabinol (THC), or placebo, administered under double-blind conditions. In our app the participants will be asked to gauge their own perceived level of impairment (as determined by self-ratings and judgments of impairment) as well as their actual impairment (as gauged by the app), providing important feedback and training about their ability to detect impairment.

NCT ID: NCT03802396 Completed - Clinical trials for Postoperative Delirium

Modulating ApoE Signalling to Reduce Brain Inflammation, deLirium and postopErative Cognitive Dysfunction

MARBLE
Start date: July 15, 2018
Phase: Phase 2
Study type: Interventional

This research study will evaluate the effectiveness and estimate the feasibility of administering an investigational drug called 'CN-105' (the study drug), to prevent postoperative cognitive decline, delirium (serious confusion) and underlying brain inflammatory and brain activity changes in adults 60 years and older undergoing surgery.

NCT ID: NCT03795454 Completed - Clinical trials for Language Development

Can Singing Kangaroo Improve Outcome of Preterm Infants

SingKang
Start date: May 3, 2013
Phase: N/A
Study type: Interventional

To assess whether a musical intervention (maternal/paternal singing) during the skin-to-skin sessions (Kangaroo care) would improve the language development of the preterm infant. Infants will be randomized to singing or silence during the Kangaroo care from the age corresponding to 30th gestational week until term age (40 gestational weeks).

NCT ID: NCT03793751 Completed - Clinical trials for Cognitive Dysfunction

Effect of Intraoperative Dexmedetomidine on Early Postoperative Cognitive Dysfunction

Start date: October 1, 2017
Phase: Phase 4
Study type: Interventional

This study will aim to identify the impact of Intraoperative dexmedetomidine infusion on POCD assessed by the Montreal Cognitive Assessment (MoCA) in geriatric patients above 60 years undergoing hip surgery under spinal anaesthesia.

NCT ID: NCT03784560 Completed - Clinical trials for Cognitive Dysfunction

Effects of Partial Sleep Deprivation on Cognitive Function of Anesthesiologists

sleep
Start date: January 2, 2019
Phase:
Study type: Observational [Patient Registry]

The purpose of this study was to evaluate differences in cognitive functions at baseline and following night shift at a trauma center among faculty anesthesiologists.

NCT ID: NCT03780621 Completed - Clinical trials for Cognitive Impairment, Mild

Effects of an Adaptogenic Extract on Electrical Activity of the Brain in Elderly Subjects With Cognitive Impairment

Start date: April 1, 2019
Phase: Phase 1
Study type: Interventional

A randomized, double-blind, placebo-controlled, two arm cross-over study to determine whether a specific combination of Andrographis paniculata and Withania somnifera can be regarded as a safe and effective treatment for cognitive deficits.

NCT ID: NCT03775941 Completed - Clinical trials for Cardiovascular Risk Factor

Fitness on White Matter and Cognition in Aging

Start date: March 2012
Phase:
Study type: Observational

Cardiorespiratory fitness (CRF) is associated with decreased risk for mild cognitive impairment (MCI) and dementia. CRF is linked with more conserved gray and white matter (WM) volume, improved WM microstructural integrity, and better cognitive performance among healthy older adults. Additional research is needed to determine: (1) which WM tracts are most strongly related to CRF, (2) whether CRF-related benefits on WM translate to enhanced cognitive functioning, and (3) factors that mediate and moderate CRF effects. Higher CRF was hypothesized to be associated with stronger WM integrity, both globally and locally in WM tracts that connect frontal brain regions. The neuroprotective effects were hypothesized to be age-dependent, such that the association between CRF and WM integrity would be stronger in old age compared to younger age. Finally, higher CRF was hypothesized to predict stronger performance on tests of executive functioning (EF), partially mediated by frontal WM integrity. Delineation of specific neurocognitive effects of CRF may serve clinicians in individually tailoring wellness interventions to meet patients' specific cognitive concerns with aging.

NCT ID: NCT03775343 Completed - Cognitive Decline Clinical Trials

Early Postoperative Cognitive Impairment in Elderly Patients Following Ocular Surgery

Start date: October 6, 2018
Phase:
Study type: Observational

This project will investigate changes in cognitive function in the early postoperative phase (<24 hours) after minor surgery in patients of older age (≥65 years).