“How about me giving blood for the COVID vaccine and not being able to get vaccinated?” A cognitive interview study on understanding of and agreement with broad consent for future use with cohort participants and guardians in Colombia and Nicaragua

Abstract excerpt

Informed consent (IC) is key to generating and maintaining research participants’ trust and upholding the ethical principle of autonomy. Broad consent for future use, wherein researchers ask participants for permission to share participant-level data and samples collected within the study for purposes loosely related to the study objectives, is central to enabling ethical data and sample reuse. Ensuring that parti...

Topics

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• Biomedical Ethics and Regulation
• Confidentiality
• Ethics in Clinical Research
• Ethics, Medical
• Genetic Predisposition to Disease
• Informed Consent
• Tissue Banks
• Tissue Donors

Identifiers and source

Literature Corpus work

6a340cc9-00f5-5464-9390-4eba3d9fc847

DOI

10.1101/2022.10.14.22281094