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Concept

Informed consent

4 studies3 discoveriesEvidence last moved Sep 20, 2026

Informed consent is the ongoing authorisation of research or treatment, not a one-time signature — including how biobanks, screening nudges and contested diagnoses strain that ideal.

Undergraduates learn a hospital consent form. These papers show why study-specific consent fails biobanks, why nudges are not harmless help, and why motives can undermine a ‘yes’.

Studies

4

Findings

3

3 supporting · 0 challenging · 0 qualifying citations

Open tensions

1

Latest change

Thirteen genomics consent forms, and what most of them left unspecified

Currently

What we know

  1. Study-specific consent fits biobanks poorly; a modified broad consent that is also ‘deep’ is argued to protect participants better.
  2. Dynamic consent is a personalised online platform so participants can be invited, updated and followed as research uses change.
  3. The help-bad-choosers defence of screening nudges is undercut by epistemic risk, including false positives, which even challenges opt-out’s automaticity.

Largest unresolved question

Broad/deep biobank consent and dynamic consent both reject one-off study-specific forms, but one leans on criteria-based protection and the other on a living digital interface.

Common misconceptions

  • A signature at enrolment settles consent for all future uses.

    Biobank and dynamic-consent papers treat uses as changing; authorisation has to be broad, deep, or revisable rather than a single frozen form.

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