Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Stephanie Niño de Rivera"'
Autor:
Natalie Benda, Sydney Woode, Stephanie Niño de Rivera, Robin B Kalish, Laura E Riley, Alison Hermann, Ruth Masterson Creber, Eric Costa Pimentel, Jessica S Ancker
Publikováno v:
Journal of Medical Internet Research, Vol 26, p e47484 (2024)
BackgroundPregnancy-related death is on the rise in the United States, and there are significant disparities in outcomes for Black patients. Most solutions that address pregnancy-related death are hospital based, which rely on patients recognizing sy
Externí odkaz:
https://doaj.org/article/c7a341fc9b9c48fab0f732862636793f
Autor:
Sabrina Mangal, Leslie Park, Meghan Reading Turchioe, Jacky Choi, Stephanie Niño de Rivera, Annie Myers, Parag Goyal, Lydia Dugdale, Ruth Masterson Creber
Publikováno v:
J Am Med Inform Assoc
Objective Participation in healthcare research shapes health policy and practice; however, low trust is a barrier to participation. We evaluated whether returning health information (information transparency) and disclosing intent of data use (intent
Autor:
Natalie Benda, Sydney Woode, Stephanie Niño de Rivera, Robin B Kalish, Laura E Riley, Alison Hermann, Ruth Masterson Creber, Eric Costa Pimentel, Jessica S Ancker
BACKGROUND Pregnancy-related death is on the rise in the United States, and there are significant disparities in outcomes for Black women. Most solutions addressing climbing pregnancy-related death rates are hospital based and rely on women recognizi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e99d5dfda6add7a59a5785bf2258f16b
https://doi.org/10.2196/preprints.47484
https://doi.org/10.2196/preprints.47484
Autor:
Sabrina Mangal, Stephanie Niño de Rivera, Jacky Choi, Meghan Reading Turchioe, Natalie Benda, Marianne Sharko, Annie Myers, Parag Goyal, Lydia Dugdale, Ruth Masterson Creber
Publikováno v:
International journal of medical informatics. 170
Research participants have a growing expectation for transparency with their collected information; however, there is little guidance on participant preferences for receiving health information and how researchers should return this information to pa