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Cognitive Dysfunction clinical trials

View clinical trials related to Cognitive Dysfunction.

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NCT ID: NCT05374642 Completed - Atrial Fibrillation Clinical Trials

Atrial Fibrillation Follow-up Investigation to Recover Memory and learnING Trial

AFFIRMING
Start date: September 19, 2022
Phase: N/A
Study type: Interventional

The objective of the study is to evaluate the effectiveness of cognitive training in people with atrial fibrillation and cognitive decline over 12-week cognitive training. Moreover, the investigators will explore whether the training effect can be maintained.

NCT ID: NCT05364216 Completed - Clinical trials for Postoperative Cognitive Dysfunction

Effect of TPVB on Postoperative Pain and Cognitive Function After VATS in Elderly Patients

Start date: May 12, 2022
Phase: N/A
Study type: Interventional

To investigate the effect of ultrasound-guided thoracic paravertebral nerve block on postoperative acute and chronic pain and cognitive function in elderly patients with thoracoscopic partial lung resection.

NCT ID: NCT05361460 Completed - Biomarkers Clinical Trials

Patients Experiences of Early Postoperative Cognition

COME
Start date: October 17, 2019
Phase:
Study type: Observational

The study has a mixed-methods design i.e. integration of qualitative and quantitative data within a single investigation. Participants included will be patients ≥60 years that are undergoing major elective joint replacement surgery (n=40) and their relative. Patient's experience of his/her cognition will be capture by interviews on postoperative day 13-16 during the follow-up visit and after 1 year. A relative will also be interviewed once on postoperative day 13-16. Cognitive function will be measured preoperatively and on postoperative day 13-16 using the International Study Group of Postoperative Cognitive Dysfunction (ISPOCD) test battery. Symptoms / discomfort will be measured pre- and postoperatively (on postoperative day 1 and 2 and at the follow up visit day 13-16) by the Swedish version of Quality of Recovery (SwQoR) and by a visual analogue scale assessing pain intensity. Biomarkers will also be collected at the same time points. The findings from the interviews will be sorted out depending on group stratification (no delayed neurocognitive recovery and delayed neurocognitive recovery). The qualitative and quantitative findings will be compared to seek for similarities and differences.

NCT ID: NCT05356988 Completed - Depression Clinical Trials

Health and Energy Through Active Living Every Day After Cancer Intervention for Cancer Survivors

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

The purpose of the Health and Energy through Active Living Every Day (HEALED) intervention, is to examine the effect of a web-based intervention on changes in device-measured physical activity (light and moderate-to-vigorous intensity aerobic) and sedentary behavior. The purpose of this study is intended for survivors of a cancer with a 5-year survival (at Stage I, II, and III) of at least 45% that has a strong level of evidence for association with physical inactivity according to the 2018 PA Guidelines Advisory Committee Report (breast, colon, endometrium, kidney, bladder, multiple myeloma). In line with social cognitive theory behavior change techniques, participants will be provided information and skills necessary to be more physically active and less sedentary after a cancer diagnosis. New materials will be disseminated biweekly through a website open only to participants, and include at-home exercise demonstration videos, research news, discussion boards, success stories, infographics for exercise recommendations, etc.

NCT ID: NCT05342727 Completed - Schizophrenia Clinical Trials

Transcranial Direct and Alternating Stimulation of the Prefrontal Cortex for Cognitive Improvement in Schizophrenia

Start date: April 1, 2021
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate different stimulation intensities and frequencies of transcranial direct and alternating current stimulation over the dorsolateral prefrontal cortex for cognitive improvement in schizophrenia.

NCT ID: NCT05341375 Completed - Clinical trials for Postoperative Cognitive Dysfunction

Effects of Thoracic Paravertebral Block Combined With S-ketamine on Postoperative Pain and Cognitive Function After Thoracoscopic Surgery

Start date: April 6, 2021
Phase: N/A
Study type: Interventional

To investigate the effect of ultrasound-guided thoracic paravertebral nerve block combined with intraoperative infusion of s-ketamine on postoperative acute pain and cognitive function in patients with thoracoscopic surgery

NCT ID: NCT05338749 Completed - Clinical trials for Cognitive Dysfunction

Computer Cognitive Training for Post-acute COVID-19 Syndrome

PACS-Cog
Start date: April 26, 2022
Phase: N/A
Study type: Interventional

This study will assess the acceptability, feasibility, and impact of game-based computer-delivered cognitive training on cognitive function in persons with cognitive symptoms that persist after recovery from acute coronavirus-19 (COVID) infection.

NCT ID: NCT05336942 Completed - Clinical trials for Mild Cognitive Impairment

Correlation Between Prognosis of Mild Cognitive Impairment and Hearing Function in Community Elderly

Start date: November 1, 2020
Phase:
Study type: Observational

Cognitive dysfunction is a high incidence disease in the elderly. To date, there is no effective treatment. At the same time, early cognitive impairment is easy to be ignored, delayed intervention. Most patients develop moderate or severe dementia with hearing loss before treatment. At present, there are few studies on the correlation between mild cognitive impairment and hearing function. The investigators evaluated CDR, MMSE, MoCa, and hearing tests at baseline, 6 months later, and 12 months later in a multicenter, randomized cohort study of adults aged 55-65 years. To investigate the correlation between mild cognitive impairment and hearing impairment and its possible predictors. The investigators hope to provide more evidence-based evidence for early identification of mild cognitive impairment.

NCT ID: NCT05330260 Completed - Surgery Clinical Trials

Five Years Follow-up of Neurological Outcome After Minimally Invasive Cardiac Surgery

FUNOMICS
Start date: March 25, 2022
Phase:
Study type: Observational [Patient Registry]

A monocenter observational study will be started to investigate postoperative cognitive dysfunction 5 years after minimally invasive cardiac surgery. Postoperative cognitive dysfunction will be evaluated in three groups: an endoscopic-CABG group (endo-CABG), a PCI (Percutaneous Coronary Intervention) group and a healthy control group. It is hypothesized that the endo-CABG group will show a stronger postoperative cognitive dysfunction compared to the PCI group and the healthy control group.

NCT ID: NCT05329272 Completed - Quality of Life Clinical Trials

Virtual Reality Training Intervention on Cognitive Function and Quality of Life

Start date: January 2017
Phase: N/A
Study type: Interventional

The present study aimed to investigate the effects of a Virtual Reality cognitive training intervention (VRCTI) on cognitive function changes measured with a cognitive test battery and improvement of quality of life in older adults with cognitive impairment in long-term care facilities. Weekly 1-hour sessions were implemented over 8 weeks targeting sustained and selective attention, memory, cognitive functions, and rule deduction. The passive control group received usual care.