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Cognitive Dysfunction clinical trials

View clinical trials related to Cognitive Dysfunction.

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NCT ID: NCT04737733 Completed - Dementia Clinical Trials

Effects of a Dementia-friendly Program

Start date: November 22, 2018
Phase: N/A
Study type: Interventional

Frail older persons with cognitive impairment are at special risk of experiencing delirium during acute hospitalisation. The purpose of this study was to investigate whether a dementia-friendly hospital program contributes to improved detection and management of patients with cognitive impairment and delirium.

NCT ID: NCT04736355 Recruiting - Clinical trials for Mild Cognitive Impairment

DAOIB for the Treatment of Mild Cognitive Impairment

Start date: January 1, 2020
Phase: Phase 2
Study type: Interventional

NMDA neurotransmission plays an important role in learning and memory. NMDA receptor-enhancing agent improved the cognitive function of patients with early-phase Alzheimer's disease. This study is a randomized, double-blind, placebo-controlled drug trial. All subjects will be allocated randomly to 2 groups: (1) DAOIB group; (2) placebo group. The study period is 24 weeks. The investigators hypothesize that DAOIB may yield better efficacy than placebo for cognitive function in patients with mild cognitive impairment.

NCT ID: NCT04736017 Recruiting - Parkinson Disease Clinical Trials

Auditory Slow Wave Enhancement in Parkinson Disease and Mild Cognitive Impairment

PDMCI-TS
Start date: April 1, 2021
Phase: N/A
Study type: Interventional

The study aims to assess the efficacy of auditory slow-wave sleep (SWS) enhancement in PD patients and patients with amnestic MCI. Patients will be randomized to two groups: Group 1 will first be treated with auditory stimulation for two weeks and then - after a washout period - switched to two weeks of sham stimulation. Group 2 will first receive sham stimulation for two weeks and then - after a washout period - switch to two weeks of auditory stimulation treatment. The washout period in between will be 2-4 weeks.

NCT ID: NCT04733989 Completed - Alzheimer Disease Clinical Trials

A Biomarker Database to Investigate Blood-Based and Digital Biomarkers in Participants Screened for Alzheimer's Disease (Bio-Hermes)

Start date: April 21, 2021
Phase:
Study type: Observational

The purpose of this study (Bio-Hermes) is to develop a blood, digital, and brain amyloid PET scan biomarker database that can be used to determine whether a meaningful relationship exists between digital tests, blood amyloid-beta, p-tau, and neurofilament biomarker levels and amyloid-beta levels identified through brain amyloid PET images. Blood collected will also be genetically sequenced to gain insights about genes and brain amyloid. The Bio-Hermes study will include 1,000 volunteers over the age of 60 screened for Preclinical Alzheimer's Disease, Prodromal AD, or Mild Dementia AD, and includes an endpoint enrollment requirement of 200 participants from underrepresented minority populations.

NCT ID: NCT04732312 Terminated - Clinical trials for Age-related Cognitive Decline

Impact of Formal Home Help on Quality of Life for Caregivers of Elderly Patients With Neurocognitive Impairment

PIAF-QVA
Start date: March 19, 2019
Phase:
Study type: Observational

The purpose of this prospective monocenter observational study is to assess the impact of the first introduction of formal home help (personalized autonomy allowance for seniors) on the quality of life of home caregivers of elderly patients with neurocognitive impairment.

NCT ID: NCT04730635 Completed - Clinical trials for Mild Cognitive Impairment

Cognition Platform Study in Participants at Risk for Alzheimer's Disease (AD) (MK-0000-413)

Start date: March 23, 2021
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to assess the ability of a repeated high-frequency site-based computerized cognitive assessment to evaluate the potential treatment effects of donepezil (MK-0000) compared with placebo among participants with mild cognitive impairment (MCI) or mild Alzheimer's Disease (AD). The primary study hypothesis is that the average percentage of correct responses on one card learning (OCL) task will be ≥2 percentage points in participants receiving donepezil compared with participants receiving placebo.

NCT ID: NCT04730596 Completed - Clinical trials for POCD - Postoperative Cognitive Dysfunction

Cognitive Dysfunction After Cataract Surgery

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

- Cataract surgery is commonly performed in elderly patients who are at high risk for developing postoperative cognitive dysfunction. Most cataract surgeries are performed under peribulbar or retrobulbar anesthesia, however, most of the patients require sedation to relieve the perioperative anxiety and induce amnesia. So, many sedative agents can be used especially benzodiazepines which may increase the risk of developing postoperative cognitive dysfunction. - Ketamine can be used as a sedative and analgesic agent in a dose of 0.25 -0.5 mg/kg with certain studies suggesting that it may decrease the risk of postoperative cognitive dysfunction. Similarly, dexmedetomidine can be used as a sedative and analgesic agent with the possibility of decreasing the incidence of postoperative cognitive dysfunction. - this controlled study will compare the effect of ketamine or dexmedetomidine on the POCD of patients undergoing cataract surgery.

NCT ID: NCT04727450 Not yet recruiting - Cognitive Decline Clinical Trials

Effects of Multimodal Training of Combined Cognitive and/or Physical Training on Cognition and Fitness of Older Adults

MTCCP
Start date: April 1, 2021
Phase: N/A
Study type: Interventional

The elderly population worldwide is expected to increase exponentially. There will be a higher percentage of older adults suffering cognitive decline in the coming decades. Cognitive impairment, being the most common health problem associated with ageing, contributes to possible loss of functional independence and disability. The purpose of this study is to determine the effectiveness of four mixed modalities of three training programs (combined cognitive and physical training [CCPT], cognitive or physical training only) on cognition and fitness of community-dwelling older adults in Hong Kong. The study hypotheses will be set as the integrated format of all three training will have higher cognition and fitness scores than other combinations of two training modes and all these mixed modalities will have greater positive outcomes than the active control subjects.

NCT ID: NCT04723667 Completed - Clinical trials for Mild Cognitive Impairment

Effects of an Empowerment-based Psycho-behavioral Program on Persons With Mild Cognitive Impairment

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

This study aims to evaluate the effects of a 13-week empowerment-based psycho-behavioral program to improve neuropsychiatric symptoms, cognitive functions, and health-related quality of life among persons with mild cognitive impairment. Its feasibility will be first evaluated in a pilot study and subsequently in a randomized controlled trial (RCT)

NCT ID: NCT04721093 Completed - Clinical trials for Mild Cognitive Impairment

Effects of Photobiomodulation on Changes in Cognitive Function and rCBF in MCI

Start date: December 12, 2019
Phase: N/A
Study type: Interventional

This pilot study has two goals. The first is to see if the cognitive improves when VA and CA are stimulated in MCI patients, and the second is to do an explanatory data analysis to see if that improves cognitive in relation to the rCBF improvement.