Implement and Test Visual Consent Template and Process

Inclusion Criteria21

• Eligibility Criteria for Patients:
• Adult participants (18+) eligible for one of three participating trials at Washington University, University of Utah, or University of North Carolina at Chapel Hill. The eligibility criteria for the main trials are below:
• UNC:
• Written informed consent was obtained to participate in the study and HIPAA authorization for release of personal health information.
• Participant is willing and able to comply with study procedures based on the judgment of the investigator.
• Age ≥ 18 years at the time of consent.
• Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1.
• Consent to a mandatory pre-study biopsy if archival tissue is not available or sufficient.
• Participants with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen.
• Washington University:
• Returning Research Results That Indicate Risk of Alzheimer Disease Dementia to Healthy Participants in Longitudinal Studies (WeSHARE)
• Participants of the Knight Alzheimer Disease Research Center.
• Participants with available results from an Alzheimer Disease blood biomarker test.
• Participants who agreed to be contacted for additional research studies.
• University of Utah:
• Huntsman Cancer Institute Total Cancer Care
• Participants who have been diagnosed with any type of tumor or cancer.
• Participants with genetic predispositions or family history of cancer or tumors.
• Participant volunteers willing to share samples and data for research.
• Eligibility Criteria for Research Staff:
• Research staff/coordinators of one of the three participating trials at Washington University, University of Utah, or University of North Carolina at Chapel Hill.