The purpose of this clinical study is to investigate the safety and efficacy of deep brain stimulation (DBS)as a treatment option for patients with cognitive, behavioral, and functional disability of Alzheimer's disease.
Open label pilot study * Expected direct benefit on the modulation of neuronal networks. * Expected indirect benefit via potential enhancements of memory, executive functions, cognition behavioral control, and functional abilities. Up to 10 subjects will be implanted with bilateral DBS systems, participants are expected to be on study for about 23 months. * Develop a multidisciplinary clinical research protocol to evaluate the efficacy of ventral striatum, nucleus accumbens, and internal capsule for the amelioration of disability caused by Alzheimer's Disease. * Enroll up to 10 patients into an open label study to evaluate the safety and efficacy of DBS for Alzheimer's Disease patients with mild to moderate disability. * Determine an initial DBS titration and stimulation settings protocol for use in subsequent controlled trials. * Evaluate the outcomes of this study based on clinical, laboratory, biomarker, imaging, cognitive, behavioral, and functional assessments. * Determine what domains of cognitive, behavioral and functioning impairment show the greatest response to DBS. * Examine the potential benefit of stimulation combined with behavioral and rehabilitation interventions in comparison to stimulation alone. * Evaluate the influence of DBS on physiological and functional changes in cortical and subcortical networks.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Enrollment
3
Implanted device
Wexner Medical Center at the Ohio State University
Columbus, Ohio, United States
Clinical Dementia Rating Scale
Time frame: 24 months
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