Lauren R Sankary
Biographic Data
| ID | 9747972 |
|---|---|
| NAME | Lauren R Sankary |
| GIVEN NAMES | Lauren R |
| FAMILY NAME | Sankary |
| SIGNATURE | SANKARY L R |
| AFFILIATIONS | Cleveland Clinic |
| ORCID | 0000-0002-9698-3616 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2021 |
| LATEST PUBLICATION YEAR | 2023 |
| H-INDEX | 0 |
Overcoming barriers to informed consent in neurological research
The ethical recruitment of participants with neurological disorders in clinical research requires obtaining initial and ongoing informed consent. The purpose of this study is to characterize barriers faced by research personnel in obtaining informed consent from research participants with neurological disorders and to identify strategies applied by researchers to overcome those barriers. This study was designed as a web-based survey of US researc…
Incorporating Stakeholder Perspectives on Scarce Resource Allocation
The coronavirus disease (COVID-19) crisis provoked an organizational ethics dilemma: how to develop ethical pandemic policy while upholding our organizational mission to deliver relationship- and patient-centered care. Tasked with producing a recommendation about whether healthcare workers and essential personnel should receive priority access to limited medical resources during the pandemic, the bioethics department and survey and interview meth…
No prominent works on this page.
Incorporating Stakeholder Perspectives on Scarce Resource Allocation
The coronavirus disease (COVID-19) crisis provoked an organizational ethics dilemma: how to develop ethical pandemic policy while upholding our organizational mission to deliver relationship- and patient-centered care. Tasked with producing a recommendation about whether healthcare workers and essential personnel should receive priority access to limited medical resources during the pandemic, the bioethics department and survey and interview meth…
Overcoming barriers to informed consent in neurological research
The ethical recruitment of participants with neurological disorders in clinical research requires obtaining initial and ongoing informed consent. The purpose of this study is to characterize barriers faced by research personnel in obtaining informed consent from research participants with neurological disorders and to identify strategies applied by researchers to overcome those barriers. This study was designed as a web-based survey of US researc…
Medicine (2 works) · Alternative medicine (1 work) · Applied Psychology (1 work) · Bioethics (1 work) · Business (1 work) · Deliberation (1 work) · Dilemma (1 work) · Disaster Management and Resilience (1 work) · Disaster Response and Management (1 work) · Disease (1 work)