Dementia Signal Development Study of Nautilus NeuroWave TM for the Detection of Dementia
NCT ID: NCT02333942
Last Updated: 2019-09-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
41 participants
OBSERVATIONAL
2014-05-31
2015-02-28
Brief Summary
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Detailed Description
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As this study is a feasibility study intended to determine whether the Nautilus NeuroWave is able to generate distinctive signals correlated with dementia, statistical analysis will not be required. Similarly, the study has not been powered to attain any particular level of statistical significance. Subsequent studies will measure sensitivity and specificity of any resulting dementia signal pattern generated by this study. These future studies will be subject to statistical analysis.
The Jan Medical Nautilus NeuroWaveTM (NNW) is a non-invasive device designed to evaluate brain oscillation patterns or the brain's pulse, generated by cardiac cycle induced intracranial blood flow. The objective of the evaluation is to determine whether the oscillation pattern is normal, whether it has been disrupted, and, if disrupted, what particular disruption pattern is evident. Various cerebral pathologies studied to date with the NNW demonstrate distinct disruption patterns. These pathologies include vasospasm, concussion and arterio-venous malformation (AVM). The objective of this study is to evaluate the brain oscillation patterns from subjects with MCI, Frontotemporal dementia, AD and from a small cohort of age matched normal controls and determine whether they exhibit pattern disruption and, if so, to quantify and categorize the distinct disruption patterns. How the Nautilus NeuroWave accomplishes this is explained later in the device description section of the protocol.
Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Alzheimer's Disease
Nautilus NeuroWaveTM System'
Nautilus NeuroWaveTM System
A noninvasive device to detect dementia utilizing headset and sensors
Mild Cognitive Impairment
Nautilus NeuroWaveTM System'
Nautilus NeuroWaveTM System
A noninvasive device to detect dementia utilizing headset and sensors
Frontotemporal Lobar Degeneration
Nautilus NeuroWaveTM System'
Nautilus NeuroWaveTM System
A noninvasive device to detect dementia utilizing headset and sensors
Age-Matched Controls
Nautilus NeuroWaveTM System'
Nautilus NeuroWaveTM System
A noninvasive device to detect dementia utilizing headset and sensors
Interventions
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Nautilus NeuroWaveTM System
A noninvasive device to detect dementia utilizing headset and sensors
Eligibility Criteria
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Inclusion Criteria
2. Have undergone some neurologic imaging
3. Age match normal subjects and subjects with symptoms consistent with MCI, FTLD or Alzheimer's disease
4. Able to understand and provide signed informed consent, or have a legally authorized representative willing to provide informed consent on subject's behalf
Exclusion Criteria
2. Not suitable for participation in this study in the opinion of the PI
3. Patients with history of other cerebral pathologies including, head trauma or prior ICH
18 Years
ALL
Yes
Sponsors
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University of California, San Francisco
OTHER
Jan Medical, Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Aimee Kao, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
University of California, San Francisco
Locations
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University of Californa San Francisco
San Francisco, California, United States
Countries
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Other Identifiers
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082189
Identifier Type: -
Identifier Source: org_study_id
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