A Study Of Exploring Health Communication Message Factors That Influence Cancer Research Recruitment

Overview

About this study

The purpose of this study is to examine how informed consent format influences patient comprehension, uncertainty, self-efficacy, and consent satisfaction.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

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.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 03/18/2026. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status
Rochester, Minn. Mayo Clinic principal investigator	Contact us for the latest status
Jacksonville, Fla. Mayo Clinic principal investigator Janice Krieger, Ph.D.	Open for enrollment

Mayo Clinic Location

Status

Rochester, Minn.

Mayo Clinic principal investigator

Contact us for the latest status

Jacksonville, Fla.

Mayo Clinic principal investigator

Janice Krieger, Ph.D.

Open for enrollment

More information

Publications

Publications are currently not available

Clinical Trials