Online registry to understand cancer experiences for patients and caregivers
Official title: Cancer Experience Registry: An Online Survey Research Study to Understand the Experiences of Cancer Patients and Caregivers
Run by Cancer Support Community, Research and Training Institute, Philadelphia · NCT02333604 · Data updated 2026-11-12
This study is trying to learn more about the experiences and needs of cancer patients and their caregivers by collecting their feedback through an online survey.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 15000 (estimated) |
| Sponsor | Cancer Support Community, Research and Training Institute, Philadelphia Academic / other |
| Locations | 1 site (Washington D.C., District of Columbia) |
| Status | Recruiting |
| Started | March 2013 |
| Main results expected | January 2035 |
| Study ends | December 2035 |
| Registry record updated | October 29, 2026 |
| Trial ID | NCT02333604 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include individuals who have received a cancer diagnosis or are caregivers for someone diagnosed with cancer.
✕Probably not a fit
Patients who do not have a cancer diagnosis or are not involved in caregiving may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The Cancer Experience Registry is an online platform designed to gather information through surveys from individuals impacted by cancer, including patients and their caregivers. It aims to explore the psychosocial needs and experiences related to cancer diagnoses, focusing on emotional, social, physical, and financial aspects. By collecting this data, the registry seeks to inform healthcare providers and policymakers about gaps in care and develop tailored programs to improve the quality of life for those affected by cancer. The findings will also be shared to enhance care and support services.
Why it matters
Potential benefit: If successful, this registry could lead to improved support programs and resources for cancer patients and their caregivers.
How similar studies have gone: Other studies focusing on patient experiences and psychosocial needs in cancer care have shown success in informing better support services.
Who can join: the full rules
Show full inclusion / exclusion 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
Where it's running
-
Cancer Support Community Research & Training Institute
Washington D.C., District of Columbia, United States Recruiting
Study contacts
- Principal investigator: Erica E. Fortune, PhD — Cancer Support Community
- Study coordinator: Olajide Fadare, PhD
- Email: ofadare@cancersupportcommunity.org
- Phone: 202.659.9709
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.