Colorectal Cancer Screening Change Package
For adults aged 45 to 85 years who do not have signs or symptoms of colorectal cancer and who do not have a personal or family history of colorectal cancer or colorectal polyps, no history of genetic syndrome such as familial adenomatous polyposis or hereditary non-polyposis colorectal cancer (Lynch syndrome), and no prior diagnosis of inflammatory bowel disease (see the U.S. Preventive Services Task Force recommendation).
Select a Focus Area
To help you make your selection, read the descriptions below or view the organizing framework in the Cancer Screening Change Packages: Overview. [PDF-787KB]
The social determinants of health focus area includes tools and resources to inform and educate about “the non-medical factors that influence health outcomes. They are the conditions in which people are born, grow, work, live, and age, and the wider set of forces and systems shaping the conditions of daily life. These forces and systems include economic policies and systems, development agendas, social norms, social policies, racism, climate change, and political systems.”1
The individual and community awareness focus area includes tools and resources to inform and educate the public about cancer, risk factors, and screening practices to increase awareness about and demand for cancer screening services.
The community-clinical linkages focus area includes tools and resources to—
- Engage community members and organizations to support screening efforts.
- Reduce structural barriers to screening in the community.
- Implement bi-directional outreach and referral between community and clinical organizations.
The capacity building for providers and staff focus area includes tools and resources for health care staff to increase knowledge and skills, improve cancer screening practices, and monitor and report on screening performance.
The screening policies, procedures, and practices within health facilities focus area includes tools and resources to assess the status of cancer screening, make cancer screening a priority, reduce structural barriers, and use data to identify patients due for screening and opportunities to improve cancer screening rates within a clinical setting or system.
The follow-up and referral focus area includes tools and resources to—
- Promote and support regular screening per USPSTF recommendations.
- Ensure timely referral for diagnostic testing, treatment, and other appropriate next steps, such as genetic testing, when screening tests are abnormal.