User Autonomy

User Autonomy is a normative ethical construct denoting the individual's right to exercise informed, voluntary control over personal data and participation in digital contact tracing systems, distinguishing it from mere data access or system usability by emphasizing self-governance and decisional independence in public health interventions.

186

Publications

8.8K

Citations

579

Authors

281

Institutions

Publications per year

2017–2026

107

Authors

579

  1. ES
    Eline Suzanne Smit

    Maastricht University, Netherlands

    3 publications · 133 citations

    3

    h-index

  2. MF
    Marianna Fotaki

    University of Warwick, United Kingdom

    3 publications · 87 citations

    3

    h-index

  3. NB
    Nadine Bol

    University of Amsterdam, Netherlands

    3 publications · 157 citations

    3

    h-index

  4. SS
    Supraja Sankaran

    Eindhoven University of Technology, Netherlands

    2 publications · 70 citations

    2

    h-index

  5. AC
    Alan Cribb

    King's College London, United Kingdom

    2 publications · 106 citations

    2

    h-index

1–5 of 579

Venues

  1. Bioethics

    4 publications · 134 citations

    4

    h-index

  2. Medicine Health Care and Philosophy

    4 publications · 146 citations

    4

    h-index

  3. AI & Society

    5 publications · 150 citations

    4

    h-index

  4. Digital Health

    3 publications · 117 citations

    3

    h-index

  5. Information Communication & Society

    ICS · 3 publications · 239 citations

    3

    h-index

1–5