The role of the Northwestern subcontract will be to the site primarily responsible for data coordination, including design of the study battery, data collection training, database creation, quality assurance, routine and safe-encrypted (HIPAA compliant) transfer of data using electronic survey software, and preliminary and final data analyses for the study aims. Ms. Curtis will serve as the site PI and will work with Dr. Kwasny and Ms. Batio to achieve these responsibilities and provide timely engagement and summaries of study findings to Dr. Arnold. Ms. Curtis and Drs. Wolf and Kwasny will also participate on weekly phone calls and travel to LSU for a site visit if necessary.
|Effective start/end date||6/1/20 → 5/31/25|
- Louisiana State University Health Sciences Center - Shreveport (21-08-003 AMD 1//5R01CA240496-02)
- National Cancer Institute (21-08-003 AMD 1//5R01CA240496-02)
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