PLoS Medicine · 2007 · 464 citations · 35 references
Public HealthClinical SciencesClinical MedicineMedical EthicsResearch EthicsClinical Trial DesignClinical Trial EthicsClinical TrialsConsentParticipant ConfidentialityStudy DesignClinical Trial DiscussionConsent In Clinical ResearchConsent In HealthcareConsent In Research EthicsConsent To Research ParticipationEthical Informed ConsentInformed ConsentResearch Participant Re-consent
Summary Points:\nA key component of informed consent to participate in medical research is the understanding that research is not the same as treatment.\nHowever, studies have found that some research participants do not appreciate important differences between research and treatment, a phenomenon called “therapeutic misconception.”\nA consistent definition of therapeutic misconception is missing from the literature, and this hinders attempts to define its prevalence or ways to reduce it.\nThis paper proposes a new definition and describes how it can be operationalized.
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