Cancer Experience Registry (CER) for Cancer Patients and Caregivers

Part of paid clinical trials in Washington D.C., District of Columbia.

Sponsor
Cancer Support Community, Research and Training Institute, Philadelphia
Study ID
NCT02333604
Status
Recruiting
Apply to this trial

Conditions

  • Cancer
  • Caregiver
  • Neoplasms

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Study Details

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 Dates

Start date
Mar 31, 2013
Status verified
Apr 2026
Primary completion
Jan 31, 2035
Completion
Dec 31, 2035

Study Design

Enrollment
15,000 participants (estimated)

Primary Outcome Measure

Self-reported quality of life measures [ Time Frame: 7 days ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Cancer Support Community Research & Training InstituteWashington D.C.District of Columbia20015
Erica E Fortune, PhD
[email protected]
202.659.9709
Claire Saxton, MBA
[email protected]
202.659.9709

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