Building a Digital Health Research Platform to Enable Recruitment, Enrollment, Data Collection, and Follow-Up for a Highly Diverse Longitudinal US Cohort of 1 Million People in the All of Us Research Program: Design and Implementation Study

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Détails bibliographiques
Publié dans:	Journal of Medical Internet Research vol. 27 (2025), p. e60189
Auteur principal:	Klein, Dave
Autres auteurs:	Montgomery, Aisha, Begale, Mark, Sutherland, Scott, Sawyer, Sherilyn, McCauley, Jacob L, Husbands, Letheshia, Joshi, Deepti, Ashbeck, Alan, Palmer, Marcy, Jain, Praduman
Publié:	Gunther Eysenbach MD MPH, Associate Professor
Sujets:	Socioeconomic status Software development Collaboration Genomics Ethnic groups Cohort analysis Software upgrading Efficacy Best practice Data collection Multimodality Leadership Research methodology Clinical outcomes Minority groups Data quality Recruitment Multisource Informed consent Computer platforms Medical research Generalizability Low income groups Computerized medical records Medical personnel Harmonization Tracking Privacy Health records Literacy Health insurance Medical records Management Research design Health care industry Health research Enrollments Institutes Implementation Ethnicity Health services Software Biomedicine
Accès en ligne:	Citation/Abstract Full Text + Graphics Full Text - PDF
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