Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
218 participants
OBSERVATIONAL
2022-01-27
2025-02-26
Brief Summary
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Detailed Description
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PRIMARY OBJECTIVES:
To estimate the proportion of individuals with MM and/or CLL who report experiencing financial difficulty in the past 12 months.
SECONDARY OBJECTIVES:
Our seventeen secondary objectives address ten aspects of patient financial experience of cancer treatment:
Financial difficulty
2.2.1 To describe the association of patient report of financial difficulty with patient reported racial identity.
2.2.2 To describe the association of patient report of financial difficulty with insurance status.
Financial navigation
2.2.3 To describe the association of patient report of financial difficulty with receiving treatment at practices that report offering patients financial guidance through navigators or social workers, and with socioeconomic status.
2.2.4 To describe the current resources dedicated to patient financial navigation at participating sites, and types of psychosocial, transportation and financial navigation interventions sites are developing.
Financial burden
2.2.5 To identify distinct patterns of financial burden among patients undergoing treatment for MM and/ or CLL.
2.2.6 To examine the relationship between distinct patterns of financial burden with patient report of financial difficulty, and with patient sociodemographic, disease and treatment characteristics.
Financial support
2.2.7 To estimate the proportion of patients with MM and/or CLL undergoing treatment who report receiving financial support in the past 12 months.
2.2.8 To describe the association of patient report of receiving financial support with receiving treatment at practices offering patients financial guidance through navigators or social workers, and with socioeconomic status.
Patient concerns regarding treatment and costs of care
2.2.9 To describe the magnitude of patient concerns regarding treatment and costs of care.
2.2.10 To describe the association of patient concerns regarding treatment and costs of care with patient sociodemographic, disease and treatment characteristics, and practice characteristics.
Patient health and well-being
2.2.11 To describe the association of financial difficulty with patient self-reported health and well-being.
Physician discussion of financial difficulties with patients
2.2.12 To estimate the proportion of individuals with MM and CLL who have received treatment in the past 12 months and report to their physician experiencing financial difficulties related to their cancer care.
2.2.13 To identify the types of financial difficulties related to cancer care that patients discuss with their provider and care team.
Physician attitudes regarding patient communication about financial difficulties
2.2.14 To describe physician attitudes or preferences for how they or the care team discuss financial difficulties with patients.
Physician use of resources for addressing financial difficulties
2.2.15 To describe the resources used by physicians and their care team to help address patient reported financial difficulties related to cancer care.
Physician perspective on the impact of COVID-19 on patient financial difficulties
2.2.16 To assess COVID-19 related disruptions to physicians' practice with respect to addressing financial difficulties in patients.
Patient experience of financial difficulties
2.2.17 To conduct semi-structured qualitative interviews with a subset of patients to elucidate the patient experience of financial difficulties over time and its impact on cancer care, and structural barriers to accessing care and/or financial assistance.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Patients with MM and/or CLL
This is a non-interventional study. All enrolled patients will complete a telephone interview. A subset of patients will complete the optional follow-up interview. The clinical practice sites through which patients are being recruited and enrolled on to the study will each complete the Site Survey. Physicians at these sites who treat patients with MM or CLL will be invited to complete the Physician Survey.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients must have current diagnosis of chronic lymphocytic leukemia (CLL) or multiple myeloma (MM)
* Patients' medical records must be available to the registering institution
* Eligible patients must have been prescribed drug-based anticancer therapy, whether administered orally or by infusion, within the prior 12 months. Specifically, eligible patients are those who:
* Are presently being treated with infused or orally-administered anticancer therapy, OR
* Completed infused or orally-administered anti-cancer therapy in the past 12 months, OR
* Were prescribed infused or orally-administered anticancer therapy within the prior 12 months yet chose to forego treatment
* Not currently enrolled in a clinical trial in which drug is supplied by the study
* Patients with psychiatric illness or other mental impairment that would preclude their ability to give informed consent or to respond to the telephone survey are not eligible
* Patients must be able to read and comprehend English or Spanish
SITE ELIGIBILITY CRITERIA
* Intent to complete the Practice Survey
* Access to patient medical records: Registering institution must have access to patient medical records, either on site or via request from other institutions, if recruiting patients at a site (as medical abstraction is required for collecting study data).
* Sites seeking to enroll Spanish- speaking patients must have Spanish speaking staff on site or through the use of a translation service to be able to conduct the informed consent discussion in Spanish.
PHYSICIAN ELIGIBILITY CRTERIA
* The physician currently treats patients with chronic lymphocytic leukemia (CLL) and/or multiple myeloma (MM).
* The physician is a treating physician at a site which has opened this protocol (LCCC 2063) and/or a site which opened the Alliance protocol (A231602CD; ClinicalTrials.gov Identifier: NCT03870633). Eligible physicians do not need to have their own patients enrolled onto this protocol.
18 Years
99 Years
ALL
No
Sponsors
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Boston University
OTHER
The Leukemia and Lymphoma Society
OTHER
UNC Lineberger Comprehensive Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Antonia Bennett
Role: PRINCIPAL_INVESTIGATOR
UNC Lineberger Comprehensive Cancer Center
Locations
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University Of Alabama At Birmingham
Birmingham, Alabama, United States
Mayo Clinic Cancer Center
Phoenix, Arizona, United States
Lewis Cancer and Research Pavilion at Saint Joseph's/Candler
Savannah, Georgia, United States
LSU Health Baton Rouge-North Clinic
Baton Rouge, Louisiana, United States
Albert Einstein College of Medicine
The Bronx, New York, United States
UNC Medical Center
Chapel Hill, North Carolina, United States
Thomas Jefferson University Hospital
Philadelphia, Pennsylvania, United States
Countries
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Related Links
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Clinical trials at UNC Lineberger
Other Identifiers
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LCCC 2063
Identifier Type: -
Identifier Source: org_study_id
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