Mayo Clinic
The goal of this clinical trial is to examine perceptions of virtual human communicators and cancer research recruitment messages. This study will also examine how different informed consent approaches influence decisions to participate in research.
Inclusion Criteria: * Able to speak, read, or understand English sufficiently to provide informed consent * 18 years of age or older * White or Black * Living in the United States Exclusion Criteria: * Unable to speak, read, or understand English sufficiently to provide informed consent * Inability on the part of the patient to understand the informed consent or be compliant with the protocol
Participants will view informed consent messaging presented in different formats
Receive a text-based informed consent form
Receive an adapted text-based informed consent form
Receive a video-based informed consent form delivered by virtual human #1
Receive a video-based informed consent form delivered by virtual human #2
Receive a video-based informed consent form delivered by virtual human #3
Receive a video-based informed consent form delivered by virtual human #4
Ancillary studies
Arctuva estimate
Actual pay is set by the research site.
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