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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

Salvato in:
Pubblicato in:Journal of Medical Internet Research vol. 27 (2025), p. e60189
Autore principale: Klein, Dave
Altri autori: Montgomery, Aisha, Begale, Mark, Sutherland, Scott, Sawyer, Sherilyn, McCauley, Jacob L, Husbands, Letheshia, Joshi, Deepti, Ashbeck, Alan, Palmer, Marcy, Jain, Praduman
Pubblicazione:
Gunther Eysenbach MD MPH, Associate Professor
Soggetti:
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
Accesso online:Citation/Abstract
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