This study is a prospective observational cohort study to document prevalence and severity of neurological symptoms among patients with confirmed or suspected novel coronavirus (COVID 19).  This study contains common data elements that all sites are requested to obtain (Tier 1 data), as well as supplemental data elements that are optional for sites to obtain retrospectively based on time and resources.  This study will also offer optional addendums to investigate Tier 2 and Tier 3 strategies, such as more invasive blood and tissue sampling, based on local resources.  If you are interested in participating, please click here: [include survey link to register]

Please note: All registered sites will receive access to study protocols and case report forms (CRF).  It is the responsibility of each study site and principal investigator to submit these documents to their institutional officials to obtain the required ethical and organizational approvals before collecting any data.

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* 1. Site Principal Investigator

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* 2. Email of Site Principal Investigator

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* 3. Telephone Number of PI

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* 4. Secondary Contact Email

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* 5. Secondary Contact Telephone Number

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* 6. Name of Institution

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* 7. Location of Institution

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* 8. Does your institution accept a central IRB?

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