Cancer Experience Registry (CER) for Cancer Patients and Caregivers

Recruiting now

Conditions studied: Neoplasms, Cancer, Caregiver

In brief

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.

Key facts

Study ID

NCT02333604

Run by

Cancer Support Community, Research and Training Institute, Philadelphia

People needed

15000

Starts

2013-03-01

Expected to finish

2035-12-01

Last updated by the study team

2026-04-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• None

Where it is running

• Cancer Support Community Research & Training Institute — Washington D.C., District of Columbia, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.