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Cancer Experience Registry (CER) for Cancer Patients and Caregivers

NCT02333604 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 15000

Last updated 2026-04-23

No results posted yet for this study

Summary

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.

Conditions

Sponsors & Collaborators

  • Cancer Support Community, Research and Training Institute, Philadelphia

    lead OTHER

Principal Investigators

  • Erica E. Fortune, PhD · Cancer Support Community

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-03-31
Primary Completion
2035-01-31
Completion
2035-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02333604 on ClinicalTrials.gov