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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Enrollment
600
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
Mayo Clinic in Florida
Jacksonville, Florida, United States
RECRUITINGSelf-efficacy (Aim 1)
Assessed by 3 questions in the study-specific survey. The questions are answered on a scale of 1 (strongly disagree) to 5=strongly agree. Higher scores indicate greater feelings of self-efficacy.
Time frame: Baseline (immediately following intervention)
Trustworthiness (Aim 2)
Assessed by a study-specific survey asking participants to rate the intervention on a scale of 1 (untrustworthy) to 7 (trustworthy). Higher scores indicate greater perception of trustworthiness.
Time frame: Baseline (immediately following intervention)
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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
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