Grants and Contracts Details
Through the two-year study period, Dr. Neyra (site PI) will: *Ensure we have local IRB approval. *Advise on the creation of an accurate phenotype and query in the electronic health records (EHR) system, execution of the data warehouse query, appropriate transformation of the EHR variables to study variables. *Link the data with national data that will be requested from the United States Renal Data System (USRDS). *Oversee the creation of a de-identified dataset containing standardized data elements using a common data/study model for transmission to the University of Alabama at Birmingham to merge with datasets from other Southeastern SHRINE consortium partners (Aim 1). *Supervise the implementation and execution of the prospective/interventional arm of the study (Aim 2). *Ensure the quality and integrity of all data collected for the purposes of this study and will directly supervise the data analysts working with the electronic data warehouse to ensure that study timelines are met each year of the proposed study. *Dr. Neyra will communicate frequently with Dr. Gutierrez and study staff at the University of Alabama at Birmingham to keep them informed about the progress of the study and any issue that might arise during the study itself. *Study data collected at the University of Kentucky will be reported to Dr. Gutierrez at the University of Alabama at Birmingham. *Throughout the study period, Dr. Neyra and his team will also be responsible for assisting the statistical analyses and interpretation of the data, and the preparation of manuscripts for publication.
|Effective start/end date||9/16/19 → 12/31/21|
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