NCT02333604Recruiting
Cancer Experience Registry (CER) for Cancer Patients and Caregivers
Cancer Experience Registry: An Online Survey Research Study to Understand the Experiences of Cancer Patients and Caregivers
Source: ClinicalTrials.gov · Last updated 29 Oct 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 15000 (estimated)
- First submitted
- 6 Jan 2015
- Start date
- Mar 2013
- Primary completion date
- Jan 2035
- Lead sponsor
- Cancer Support Community, Research and Training Institute, Philadelphia
- Diseases
- Prostate cancer, Melanoma, Bladder cancer, Chronic lymphocytic leukaemia, Acute lymphoblastic leukaemia, Chronic myeloid leukaemia, Myelodysplastic syndromes, Lung cancer, Metastatic breast cancer, Colorectal cancer, Liver and biliary tract cancer, Gastric and esophageal cancer, Multiple myeloma, Ovarian cancer, Acute myeloid leukemia
- NCT number
- NCT02333604
What you commit to
- Study type: Observational
- Planned participants: 15000
- From Mar 2013 to the primary completion date, Jan 2035
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- None
Who the study is looking for
- 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
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Cancer Support Community Research & Training Institute Coordinator of this site? Confirm its status | Washington D.C. | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.