Como consentir sem entender?

Miranda, Vanessa da Costa; Fêde, Ângelo Bezerra de Souza; Lera, Andréa Thaumaturgo; Ueda, Aline; Antonangelo, Daniela Veiga; Brunetti, Karina; Riechelmann, Rachel; del Giglio, Auro.
Rev. Assoc. Med. Bras. (1992) ; 55(3): 328-334, 2009. tab
Artículo en Portugués | LILACS | ID: lil-520189

Documentos relacionados

  1. [How to consent without understanding?].
  2. Clear aligner therapy informed consent forms: A quality and readability evaluation.
  3. Stakeholder involvement in the development of trial material for a clinical trial.
  4. Beyond translations, perspectives for researchers to consider to enhance comprehension during consent processes for health research in sub-saharan Africa: a scoping review.
  5. Continuous quality improvement: reducing informed consent form signing errors.
  6. Regulatory compliance and readability of informed consent forms in industry-sponsored drug development clinical trials.
  7. Assessing the Readability of Clinical Trial Consent Forms for Surgical Specialties.
  8. Electronic informed consent criteria for research ethics review: a scoping review.
  9. Towards objectivity in ethical assessment: legibility as part of informed consent form comprehension.
  10. Assessment of the quality of patient information sheets and informed consent forms for clinical trials at a hospital neurology service.