Stage IVA Colon Cancer Clinical Trial
Official title:
Implementation of a Prospective Financial Impact Assessment Tool in Patients With Metastatic Colorectal Cancer
This clinical trial studies the use of the financial impact assessment tool in patients with colorectal cancer that has spread from the primary site to other places in the body. Gathering information about patients with colorectal cancer over time may help doctors better understand the financial impact of cancer and help patients avoid financial problems during treatment.
PRIMARY OBJECTIVES:
I. To estimate the incidence of treatment-related major financial hardship over 12 months,
among patients with newly diagnosed metastatic colorectal cancer (mCRC) treated at Southwest
Oncology Group (SWOG)-affiliated Cancer Care Delivery Research (CCDR) components of the
National Cancer Institute (NCI) Community Oncology Research Program (NCORP) sites.
SECONDARY OBJECTIVES:
I. To describe the association of major financial hardships with mCRC treatment by
demographic factors, including age, race, marital status, employment status, and income.
II. To explore whether occurrence of major financial hardship is associated with poorer
health-related quality of life over time.
III. To profile the magnitude and timing of treatment-related changes in patients' income,
assets, debt, and employment, and to quantify major out-of-pocket expenses during the 12
months following registration.
IV. To explore the extent to which health insurance factors (e.g. high copayments,
deductibles, premiums, loss/change of insurance plan) are associated with major financial
hardship and treatment non-adherence.
V. To determine feasibility of recruiting primary caregivers and measuring caregiver burden
and caregivers' perceptions about cancer treatment costs.
VI. To determine the feasibility of conducting a prospective-multi-site longitudinal cohort
study assessing financial outcomes in patients with mCRC undergoing treatment within the
NCORP network.
TERTIARY OBJECTIVES:
I. To obtain objective measures of expenses, debt and credit through linkage with individual
patient credit reports (TransUnion) at enrollment (baseline) and end of follow up (12
months).
OUTLINE:
Patients complete questionnaires (including the Baseline, Financial/Employment Impact,
Insurance Impact, Quality of Life, and Treatment Perceptions questionnaires) over 30-60
minutes at baseline and at 3, 6, 9, and 12 months. Caregivers complete questionnaires over
30-60 minutes at baseline and at 6 and 12 months.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research
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