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When is it impractical to ask informed consent? A systematic review.

Sara Jm LaurijssenRieke van der GraafWouter B van DijkEwoud SchuitRolf Hh GroenwoldDiederick E GrobbeeMartine C de Vries
Published in: Clinical trials (London, England) (2022)
There are conditions that render conventional informed consent truly impractical, such as untraceable participants or harm for participants. At the same time, researchers have a moral responsibility to design an infrastructure in which consent can be obtained, even if they face hardship in obtaining consent. In addition, researchers should seek to minimize harm inflicted upon participants when harm may occur as a result of the consent procedure. Invalidity of research due to consent issues should not be regarded as impractical but as a condition that limits the social value of research. Further research is essential for when a waiver of informed consent based on impractical is also reasonable.
Keyphrases
  • healthcare
  • mental health
  • minimally invasive