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Cognitive Impairments clinical trials

View clinical trials related to Cognitive Impairments.

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NCT ID: NCT05896189 Recruiting - Breast Cancer Clinical Trials

Cognitive Training for Cancer Related Cognitive Impairment in Breast Cancer Survivors

Start date: February 2, 2024
Phase: N/A
Study type: Interventional

This Phase III trial will examine the efficacy of computerized cognitive training methods on perceived cognitive impairment in breast cancer survivors.

NCT ID: NCT05053204 Recruiting - Clinical trials for Cognitive Impairments

Influence Factors and Cognitive Characteristics in Unipolar and Bipolar Depression:Based on the THINC-it Tool

Start date: May 15, 2021
Phase:
Study type: Observational

Cognitive impairment is the core symptom of unipolar and bipolar depression, which seriously affects the prognosis of the disease and the rehabilitation of social function. There is no unified conclusion in the field and severity of cognitive impairment, and the cause of cognitive impairment is unknown, which may be related to many factors. In this study,the THINC-it tool was used to study the characteristics of cognitive impairment in unipolar and bipolar depression by longitudinal follow-up, which provides a theoretical basis for the differential diagnosis of unipolar and bipolar depression. Early identification and intervention of risk factors can improve the prognosis of the disease.

NCT ID: NCT04490330 Recruiting - Cirrhosis Clinical Trials

Screening for Alcohol-related Cognitive Impairments in Cirrhotic Patients

CirCo
Start date: August 1, 2020
Phase:
Study type: Observational

80% of patients with alcohol use disorders (AUD) present cognitive impairments, such as memory and executive functions. These disorders may have repercussions in addiction treatment by altering the patient's adherence to care. The level of impairment is dependent on the onset of addiction, and also the duration of abstinence. A complete neuropsychological evaluation is necessary to highlight cognitive impairments. In practice, the evaluation of these disorders by practitioners, is done with the help of tools of screening like the MoCa (Montreal cognitive assesment) and the BEARNI (Brief evaluation of alcohol related neuropsychological impairment). However, none of these tools have been evaluated in patients with alcoholic cirrhosis. Indeed, some studies have suggested that liver disorders including cirrhosis may be a factor aggravating cognitive disorders. The purpose of this study is to evaluate the ability of the BEARNI tool to detect alcohol-related cognitive problems in patients with alcohol-related cirrhosis.

NCT ID: NCT02778581 Recruiting - Alzheimer Disease Clinical Trials

Study to Evaluate the Effect of a Vegetal Oil on Cognitive Impairment

Start date: March 2016
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate the beneficial effect of a mixture of vegetal oils with a composition related to short, medium and long unsaturated chain fatty acids on patients with a diagnose of cognitive impairment or mild to moderate Alzheimer disease

NCT ID: NCT01466205 Recruiting - Clinical trials for Cognitive Impairments

Clinical Testing of a D1 Agonist for Cognitive Enhancement in Schizotypal Personality Disorder

SPD
Start date: January 2011
Phase: Phase 2
Study type: Interventional

Currently, no study to date has directly tested a selective D1R agonist in relation to the cognitive impairment of Schizophrenia without the confound of neuroleptics. The investigators propose to examine the efficacy of DAR-0100A, a highly selective, full D1R agonist supported by pre-clinical and preliminary pilot clinical data, in ameliorating the cognitive deficits in Schizotypal Personality Disordered subjects receiving no medications including antipsychotics. The investigators hypothesize that 1) Baseline primary outcome measures will be impaired in Schizotypal personality disorder (SPD) subjects compared to controls, 2) SPD subjects on DAR-0100A will show improvement on primary measures greater than healthy controls and SPD patients randomized to placebo, and 3) SPD patients will show significant improvements on primary outcome variables on drug compared to placebo.