Opt-out Consent

Opt-Out Consent is a consent mechanism in which individuals are presumed to have agreed to participate in contact tracing unless they explicitly decline, distinguishing it from opt-in models by placing the procedural burden of withdrawal on the individual rather than requiring active enrollment.

72

Publications

2.1K

Citations

321

Authors

188

Institutions

Publications per year

2017–2026

33

Variants

Presumed Consent

Authors

321

  1. RE
    Ronan E. O’Carroll

    University of Stirling, United Kingdom

    5 publications · 350 citations

    5

    h-index

  2. JM
    Jordan Miller

    University of Stirling, United Kingdom

    3 publications · 102 citations

    3

    h-index

  3. SC
    Sinéad Currie

    University of Stirling, United Kingdom

    3 publications · 102 citations

    3

    h-index

  4. MG
    Michael Gold

    The University of Adelaide, Australia

    3 publications · 88 citations

    3

    h-index

  5. AB
    Annette Braunack‐Mayer

    The University of Adelaide, Australia

    3 publications · 88 citations

    3

    h-index

1–5 of 321

Venues

  1. Journal of Medical Ethics

    5 publications · 128 citations

    5

    h-index

  2. BMJ Open

    3 publications · 77 citations

    3

    h-index

  3. PubMed

    Repository · 3 publications · 46 citations

    3

    h-index

  4. Bulletin of the World Health Organization

    2 publications · 149 citations

    2

    h-index

  5. Trials

    2 publications · 82 citations

    2

    h-index

1–5