DELPHI in Subjects at Risk for Stroke and Dementia

QuantalX Neuroscience335 enrolled

Overview

The DELPhi system is a software device that is used for the noninvasive evaluation of brain plasticity and connectivity. The DELPhi software uses EEG and TMS devices as accessories. Standard electro-physiological acquisition is performed using TMS to evoke regional neuronal potentials measured as EEG data. TMS-EEG data is analyzed with regards to conventional, well established characteristics of neuronal network plasticity and connectivity.

Transcranial magnetic stimulation (TMS) is a noninvasive brain stimulation method that allows to study human cortical function in vivo. Using TMS for examining human cortical functionality is enhanced by combining TMS with simultaneous registration of electroencephalograph (EEG). EEG provides an opportunity to directly measure the cerebral response to TMS. Measuring the cortical TMS Evoked potential (TEP), is used to assess cerebral reactivity across wide areas of neocortex. By evaluating the propagation of evoked activity in different behavioral states and in different tasks, TMS-EEG has been used to causally probe the dynamic effective connectivity of human brain networks. In this study the sponsor is intended to collect data of subjects at the ages of 50-75, at risk for stroke and dementia using DELPHI, brain MRI scans, cognitive tests and clinical and demographic information. Some of the patients agreeing to perform a second test will serve for a reliability test. Primary Objectives: 1. Definition of DELPHI's average TEP response of at risk for stroke and dementia population in subjects over 50-75 years old+/- STD. 2. Assessing the Safey of the use of DELPHI in at risk for stroke and dementia population. 3. Defining DELPHI's test-retest reliability by quantifying correlation coefficient between two tests. Exploratory objectives: 1. Evaluating the sham stimulation effect. 2. Assessing confounders effecting results. Subjects will perform a medical interview, neurological exam, cognitive evaluations, two emotional inventories and a brain MRI scan.

Study Type

OBSERVATIONAL

Enrollment

335

Conditions

Stroke

Eligibility

Sex: ALLMin age: 50 YearsMax age: 75 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion criteria: 1. Male and female at the ages of 50-75 years old (included) with at least one risk factor for Stroke or Dementia\* and/or a suspected cognitive impairment\*\* 2. Willing to cooperate with all study procedures. \*Risk factors for Stroke and Dementia: * Previous stroke or TIA * Hypertension * Dyslipidemia * Diabetes Mellitus * Atrial Fibrillation * Other cardiac conditions (such as, MI, Valve disease etc.) * Smoking (any current smokers or past heavy smokers (\>20 cigarettes/day)). * Obesity and overweight (BMI\>25) * Familial history of dementia * Age ≥ 65 * Sleep disturbances \*\* Suspected cognitive impairment: * self or family report of cognitive impairments * Objective evidence of cognitive impairments 4.2 Exclusion criteria: 1. Any neurodegenerative disease. 2. Neurological developmental disorder (e.g., Cerebral Palsy, Anoxic Brain Damage, Autism Spectrum Disorder). 3. Multiple Sclerosis (MS). 4. Major psychiatric disorders (e.g., PTSD, Bi-polar Disorder, Schizophrenia, Substance abuse), 5. Chronic pain disorders. 6. History of brain tumor, history of brain surgery or brain radiation damage. 7. Prior known epileptic episode. 8. Subjects with any metallic brain implant or fragments (such as shunt, pacemaker, clips, coils, bullet fragments, cochlear implants). 9. Subjects with any implanted devices activated or controlled by physiological signals and/or ferromagnetic or other magnetic sensitive metals implanted in the head or anywhere within 12 inches/30 cm from the stimulation coil. 10. Any contraindication to MRI. 11. With any known significant head trauma in the medical history (e.g. loss of consciousness, altered consciousness, diagnosed evidence of contusion on brain imaging following trauma. 12. Current ongoing use of opioids, anti-psychotic, or anti-epileptic medications. 13. Intake of any other CNS directed medication such as sleeping pills, SSRIs, Anxiolytics 12 hours or less prior to the DELPHI evaluation. 14. Subjects that report drug abuse. 15. Pregnant or breastfeeding woman.

Locations (4)

Diablo Clinical Research Inc.

Walnut Creek, California, United States

Neurotrials Research

Atlanta, Georgia, United States

Clinical Research Center CTI

Norwood, Ohio, United States

Sourasky Tel-Aviv Medical Center

Tel Aviv, Center, Israel

Outcomes

Primary Outcomes

Establishing DELPhI's norms of population 50-75 years old at risk for stroke and dementia

Mean, STD, standard error (SEM), coefficient of variation (CV%), minimum, median, maximum and 95% confidence interval, for every DELPHI parameter in at risk for stroke and dementia population.

Time frame: 1 visit

Establish DELPhI's safety in subjects 50-75 at risk for stroke and dementia.

Rates and Frequencies of Adverse events and descriptive report of Adverse events and possible relationship to DELPHI.

Time frame: 1 week

DELPHI's reliability

Examining DELPHI's reliability by defining Intra-Class Correlation (ICC) coefficients between two tests performed at different days and/or different operators at each of DELPHI's parameters.