Alzheimer's Disease
Conditions
Keywords
Alzheimer's Disease, Diagnosis, Neuronal function, Cognitive Impairment, Magnetoencephalography
Brief summary
This study is designed to test the hypothesis that the Synchronous Neural Interaction™ Test is useful for diagnosing Probable Alzheimer's Disease according to standard criteria. Subjects diagnosed with Alzheimer's Disease as well as age-matched normal control subjects will be evaluated for symptoms of Alzheimer's Disease and those meeting inclusion criteria will undergo a brief, non-invasive scan of brain function using a magnetoencephalography (MEG). The scan itself lasts 1 minute while the subject is asked to stare at a dot projected in front of them on a video screen. Orasi Medical believes that patterns of brain activity measured at rest are indicative of Alzheimer's Disease pathology. The protocol is amended to add a follow-up assessment for previously enrolled and completed subjects who agree to participate in the follow-up assessment approximately 9 - 15 months after initial study enrollment. Subjects who agree to participate in the follow-up assessment will undergo the same standardized tests and MEG scan procedure as completed in the initial study.
Interventions
None listed
Sponsors
Noran Neurological Clinic
Minneapolis Veterans Affairs Medical Center
Orasi Medical, Inc.
Study design
Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes
Inclusion criteria
1. Subject is between 18 and 90 years of age 2. i. Provide written informed consent for study participation, OR ii. Provide written assent to study participant accompanied by the provision of written informed by the subject's legally authorized representative (LAR); see Section 8. Informed Consent for details of the procedures use to meet these study inclusion criteria 3. Have one of the following clinical diagnoses or conditions: * Probable AD according to the NINCDS-ADRDA criteria * Possible AD according to the NINCDS-ADRDA criteria * Prodromal AD according to criteria described by Dubois & Albert (2004) * Normal control subject
Exclusion criteria
1. Have a significant non-AD neurological condition including Parkinson's Disease, Vascular Dementia, Lewy Body Dementia or Frontal Temporal Dementia, human immunodeficiency virus, multiple sclerosis, epilepsy, or severe traumatic brain injury. 2. Have dementia due to multiple etiologies (e.g. mixed dementia) 3. Show the presence of prominent disturbances in gait thought to be associated with Parkinsonism. 4. Show prominent changes in personality or social conduct prior to the onset of prominent cognitive dysfunction 5. Have a Modified Hachinski Ischemia Scale score of greater than 4 6. Have a history of primary psychotic disorder (e.g schizophrenia, schizoaffective disorder, delusional disorder) or bipolar disorder 7. Have a lifetime or current history of alcohol or substance abuse/dependence 8. Have had an MRI two weeks prior to completing the MEG scan 9. Have metal braces or pacemaker that may interfere with the MEG scan 10. Are unable to complete the MEG scan procedure Follow-up Assessment Inclusion Criteria: Subjects who completed Protocol ADG 08-01 will be contacted and invited to participate in the follow-up assessment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sensitivity and specificity for test under investigation to diagnose probable Alzheimer's Disease. | Immediately |
Countries
United States
Outcome results
None listed