Cancer Experience Registry (CER) for Cancer Patients and Caregivers

Launched by CANCER SUPPORT COMMUNITY, RESEARCH AND TRAINING INSTITUTE, PHILADELPHIA · Jan 6, 2015

Keywords

ClinConnect Summary

The Cancer Experience Registry (CER) is an online study designed to learn more about the experiences of people affected by cancer, including patients and their caregivers. The study collects information through surveys that ask about various aspects of living with cancer, such as emotional challenges, physical health, financial concerns, and the decision-making process. By gathering this information, the researchers hope to improve care and support for cancer patients and their families in the future.

To participate in this study, you should have been diagnosed with cancer or be a caregiver for someone who has. Caregivers can be family members or friends who help support someone with cancer. This study is open to adults aged 65 and older living in the United States, its territories, or Canada, who can read and understand English. There are no specific exclusions, so if you meet the criteria, you are welcome to join. As a participant, you can expect to fill out surveys that reflect your experiences, and your responses will help shape future cancer care and support programs.

Gender

ALL

Eligibility criteria

• Inclusion criteria:
• • Have received a cancer diagnosis or have been a family caregiver or informal caregiver (i.e., a relative or friend) for someone diagnosed with cancer
• • Live in United States, a US territory, or Canada
• • Able to read and understand English
• Exclusion criteria:
• • None