Cancer Experience Registry (CER) for Cancer Patients and Caregivers
Recruiting · NCT02333604 · Observational (researchers observe without assigning treatment) · Lead sponsor: Cancer Support Community, Research and Training Institute, Philadelphia
View the official record on ClinicalTrials.gov →What this trial is about
The Cancer Experience Registry®: An Online Survey Research Study to Understand the Experiences of Those Impacted By a Cancer Diagnosis. The Registry is a web-based platform to distribute cross-sectional and longitudinal surveys. Study surveys are designed based on input from advisor experts, including patients and caregivers, and focus on the social, emotional, physical, financial and decision-making experiences of those who have been diagnosed with cancer and their caregivers. Findings contribute toward enhancing care for patients, survivors and caregivers via programming and policy initiatives.
Who can take part
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
Where it is running
3 locations listed across 1 US state.
- Cancer Support Community Research & Training Institute - Washington D.C., District of Columbia, United States
- Cancer Support Community Research & Training Institute - Washington D.C., District of Columbia, United States
- Cancer Support Community Research & Training Institute - Washington D.C., District of Columbia, United States