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Dementia of Alzheimer Type clinical trials

View clinical trials related to Dementia of Alzheimer Type.

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NCT ID: NCT06245031 Enrolling by invitation - Alzheimer Disease Clinical Trials

Extension to a Pivotal Study of Sensory Stimulation in Alzheimer's Disease (OLE Hope Study, CA-0015)

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

This is an open-label extension for a multicenter, randomized, double-blind, sham-controlled, adaptive design pivotal study. Participants who complete the Hope Study (CA-0011) will be eligible to consent for screening to enroll in the OLE Hope Study (CA-0015). All participants will be treated with an Active Sensory Stimulation System (GS120) for 60 minutes daily for up to 12 months. There will be no Sham treatment group or randomization involved in this study.

NCT ID: NCT05973448 Enrolling by invitation - Alzheimer Disease Clinical Trials

The Nightlight Falls Prevention Study

Start date: July 28, 2023
Phase: N/A
Study type: Interventional

This project will test the effectiveness of a novel intervention consisting of unobtrusive, low-intensity, horizontal and vertical lights that outline the bathroom or entry way doorframe in residents' rooms and provide visual cues to promote postural stability. Specifically, this pragmatic crossover trial will enroll 390 assisted living residents with dementia and follow them for one year, comparing the incidence of nighttime falls during the lighting condition to the incidence of falls during the control condition; secondarily, it will determine whether and to what extent the intervention effect is modified by resident- and environmental-level risk factors, and satisfaction with the lighting system.

NCT ID: NCT04851691 Enrolling by invitation - Alzheimer Disease Clinical Trials

An Electronic Clinical Decision Support Tool to Reduce Low-value Antipsychotic Prescriptions

Start date: August 3, 2021
Phase: N/A
Study type: Interventional

The goal of this study will be to design, implement and test the impact of a quality improvement (QI) intervention that uses an EHR CDS tool among physicians newly ordering an antipsychotic medication for older adults with ADRD. The study team hypothesizes that the intervention will reduce each participating clinician's pill days per patient prescribed.