Breast Cancer Clinical Trial
Incorporating ePrognosis for the Encouragement of Smarter Screening for Breast and Colorectal Cancer in Older Adults
Summary
This clinical trial assesses the feasibility and acceptability of a smarter screening intervention for breast and colorectal cancer in older adults. This study aims to learn more about how to support patients and physicians in making cancer screening decisions for older adults.
Full Description
PRIMARY OBJECTIVES:
I. Complete development of and refine "Smarter Screening", a multi-component, patient-centered intervention centered around ePrognosis: Cancer Screening to facilitate shared decision-making screening discussions for breast and colorectal cancer in older adults.
II. Assess feasibility and acceptability of the "Smarter Screening" intervention and assess its impact versus usual care on shared decision-making about whether or not to continue breast and colorectal cancer (CRC) screening among multi-ethnic and socioeconomically diverse primary care patients.
EXPLORATORY OBJECTIVES:
I. Impact on breast and CRC screening versus usual care.
II. Risk perception, worry, and a patient-reported measure of decision quality.
OUTLINE: Participants are randomized to 1 of 2 arms.
ARM I: Participants receive Passport to Health booklet and complete ePrognosis before scheduled primary care visit.
ARM II: Participants receive usual care before scheduled primary care visit.
After completion of study, participants are followed up at 1 week post primary care visit.
Eligibility Criteria
Inclusion Criteria:
Age 70 years and above
Ability to understand study procedures and to comply with them for the entire length of the study
Ability of individual to understand a written informed consent document, and the willingness to sign it
Have no prior history of cancer
Scheduled for an upcoming appointment in University of California, San Francisco (UCSF) General Internal Medicine or Women's Health Primary Care clinics
English-speaking
Exclusion Criteria:
Contraindication to any study-related procedure or assessment
Non-English speaking
Are under the current medical care of either the study primary investigator (PI) or co-investigator (Co-I)
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There is 1 Location for this study
San Francisco California, 94143, United States
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