Cancer Experience Registry (CER) for Cancer Patients and Caregivers
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
About the trial
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.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Mieć postawioną diagnozę raka lub być opiekunem rodzinnym/nieformalnym (rodzina lub przyjaciel) osoby z diagnozą raka
- •Mieszkać w Stanach Zjednoczonych, terytoriach USA lub Kanadzie
- •Umieć czytać i rozumieć język angielski
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- April 23, 2026
- Sex
- No restrictions
Locations (1)
Cancer Support Community Research & Training Institute
Washington D.C., United States
Trial contact
Erica E. Fortune, PhD
Kara Doughtie, PhD
Contact information from ClinicalTrials.gov. Contact in English.
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/1/2026.
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