Alzheimer Disease Clinical Trial
Official title:
Feasibility Study of Transcranial Ultrasound Stimulation on Alzheimer's Disease Patients
Currently, the main treatment method for Alzheimer's disease (AD) is chemotherapy. However, the effectiveness of drugs is moderate and there are several side effects. In this clinical trial, the investigators would like to activate the brain by the transcranial ultrasound stimulation (TUS). This is a feasibility study to evaluate the safety and initial effectiveness of TUS for the treatment of patients with mild AD.
The purpose of this study is to verify the feasibility of low intensity transcranial
ultrasound stimulation (TUS) for patients with mild Alzheimer's disease (AD). As a secondary
aim, the investigators will explore whether the TUS is associated with improvement in
cognitive functioning six and forty-six weeks following the intervention.
Subjects will be randomly assigned to one of two experimental groups which with or without
the TUS administration.
The investigators will study up to 20 subjects with mild AD. Initially, subjects will undergo
a screening assessment with a study physician to determine medical and psychiatric history,
establish AD diagnosis, and undergo a bold draw. Subjects that meet criteria and agree to
participate in the study will undergo a follow-up visit. In the baseline measurement visit,
participants will first undergo neuropsychological testing. Participants will be randomly
assigned to one of two groups. Participants will then be administrated TUS treatment for six
weeks. Subsequently, participants will undergo a series of neuropsychological test. A final
follow-up assessment will be administered at forty-six weeks.
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