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NCT02333604 | RECRUITING | Neoplasms


Cancer Experience Registry (CER) for Cancer Patients and Caregivers
Sponsor:

Cancer Support Community, Research and Training Institute, Philadelphia

Information provided by (Responsible Party):

Erica E. Fortune

Brief 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.

Condition or disease

Neoplasms

Cancer

Caregiver

Detailed Description:

The aims of the Registry are to: 1) better understand the psychosocial experiences and needs of people who have been impacted by cancer, including patients, survivors and caregivers; 2) inform the research community, healthcare providers, patient advocates and policy makers around gaps in care and the psychosocial challenges of people affected by cancer; 3) use the findings to develop and disseminate tailored (data-guided) programs and services that will address the emotional and social needs and ultimately improve the long-term quality of life of people affected by cancer; 4) link registrants to cancer related resources and programs via an online, modifiable platform; and 5) provide collaborating sites (e.g., hospitals/health networks/CSC affiliates) with aggregated reports on quality and needs of members or customers to enhance or improve quality of care. Findings from the Registry are disseminated online at https://www.cancersupportcommunity.org/sites/default/files/file/2020-07/CSC_Registry_Report_June_2020.pdf

Study Type : OBSERVATIONAL
Estimated Enrollment : 15000 participants
Official Title : Cancer Experience Registry: An Online Survey Research Study to Understand the Experiences of Cancer Patients and Caregivers
Actual Study Start Date : 2013-03
Estimated Primary Completion Date : 2035-01
Estimated Study Completion Date : 2035-12

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: 1
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

Cancer Experience Registry (CER) for Cancer Patients and Caregivers

Location Details

NCT02333604


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How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations


RECRUITING

United States, District of Columbia

Cancer Support Community Research & Training Institute

Washington, District of Columbia, United States, 20015

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