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Clinical Trials in Mexico / NCT04960787
Active, not recruiting Not applicable

Financial Navigation Program to Improve Understanding and Management of Financial Aspects of Cancer Care for Patients and Their Spouses

NCT04960787 · tracked via the Priya Life Science Mexico tracker
Phase
Not applicable
Started
2021-10-12
Last updated
2026-05-14

Condition(s) studied

Hematopoietic and Lymphoid Cell NeoplasmMetastatic Malignant Solid NeoplasmRecurrent Malignant Solid Neoplasm

Investigational drug(s) / intervention(s)

Educational InterventionPatient NavigationQuality-of-Life AssessmentQuestionnaire Administration

Educational Intervention: Watch online educational videos

Patient Navigation: Meet with CENTS counselor and PAF case manager

Quality-of-Life Assessment: Ancillary studies

Questionnaire Administration: Complete questionnaires

Study summary

This clinical trial examines a financial navigation program in helping patients (and their spouses or partner caregivers, if participating) understand and better manage the financial aspects of cancer care. Cancer patients and their spouse/partner caregivers may be at high risk for financial problems because of the cost of cancer treatment. A financial navigator is a person or team who works with patients and their families to help them reduce stress or hardship related to the cost of cancer treatment. Financial navigators help patients understand their out-of-pocket expenses and what their health insurance plans may cover. Financial navigation may also help patients set up payment plans, find cost-saving methods for treatments, and improve access to healthcare services that the patient needs. Providing financial navigation to patients may help reduce financial worries and improve quality of life.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Patients must have a diagnosis of a metastatic solid tumor or a hematologic malignancy and must receive anti-cancer treatment (i.e. chemotherapy, hormonal therapy, targeted therapy, biologic therapy, immune therapy, bone marrow transplant). Registration must occur within 180 days after diagnosis of metastatic or stage IV solid tumor or treatment-requiring hematologic malignancy. Patients with indolent hematologic diseases undergoing observation alone are not eligible; patients with previously diagnosed hematologic cancers progressed to the point of requiring systemic therapy are eligible, so long as the progression occurred within the previous 180 days. Biopsy confirmation of metastatic disease is not required * Patients with recurrent solid tumors will be allowed as long as 1) this is the first presentation of metastatic disease and 2) the diagnosis of the metastasis is at least 180 days (6 months) after the diagnosis date of the previous earlier stage cancer * Patients with a history of secondary malignancy are allowed as long as they were not diagnosed within the previous 24 months, are not on active therapy, and are disease-free. Patients with adequately treated basal cell or squamous cell skin cancer, and in situ cervical cancer at any point prior to enrollment are eligible * Patients who have started anti-cancer treatment for the current diagnosis must have started within 90 days prior to registration * Patients who are planning to start anti-cancer treatment for the current diagnosis must start within (=\<) 30 days after registration * Patients are allowed to be co-enrolled on other clinical trials (including non-treatment studies and studies that may or may not include investigational drugs) * Patients must be at least 18 years of age * Patients must have a Zubrod performance status of 0-2 * Patients must complete the baseline patient reported outcomes (PRO) questionnaires prior to registration and must be able to complete questionnaires in English or Spanish * Patients must provide their full name, primary address in the United States (U.S.), birth date and social security number at registration for the purposes of accessing credit report data. (This may be obtained directly from the patient, study questionnaires, or the medical record) * Patients must provide email and/or telephone number for the purposes of being contacted by financial navigators Spouse/partner caregiver participation is optional. * Spouse/partner caregiver must be living in the same household as the eligible patient and be either legally married, in a common law marriage, or be an intimate partner/significant other of the participant\* * Spouse/partner caregivers must be at least 18 years of age * Spouse/partner caregivers must provide their full name, primary address in the U.S., birth date and social security number at registration for the purposes of accessing credit report data * Spouse/partner caregivers must provide email and/or telephone number for the purposes of being contacted by the financial navigators * Spouse/partner caregivers must be able to complete questionnaires in English or Spanish and must complete the baseline questionnaires prior to patient registration \*The study team acknowledges that other types of caregivers may also face financial hardship following a patient's cancer diagnosis and may similarly benefit from financial education and navigation. The decision to focus solely on spouse or partner caregivers was scientific, to understand how caregivers who share household finances experience financial hardship. * Participants (patients and caregivers, when participating) must sign and give written informed consent in accordance with institutional and federal guidelines. Use of legally-authorized representative is not permissible for this study. Documentation of informed consent via remote consent is permissible * As a part of the Oncology Patient Enrollment Network (OPEN) registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system Exclusion Criteria: * Patients may not be enrolled in hospice care at the time of registration * Non-spouse/partner caregivers such as friends, adult children, parents, or other relatives living in the same household as the patient are not eligible

Primary outcome measure(s)

Trial sites (266)

FacilityCityRegionStatus
Fairbanks Memorial Hospital Fairbanks Alaska
Mercy Hospital Fort Smith Fort Smith Arkansas
Kaiser Permanente-Deer Valley Medical Center Antioch California
Epic Care-Dublin Dublin California
Kaiser Permanente Dublin Dublin California
Epic Care Partners in Cancer Care Emeryville California
Kaiser Permanente-Fremont Fremont California
Kaiser Permanente-Fresno Fresno California
Contra Costa Regional Medical Center Martinez California
Kaiser Permanente-Modesto Modesto California
Kaiser Permanente-Oakland Oakland California
Kaiser Permanente- Marshall Medical Offices Redwood City California
Kaiser Permanente-Richmond Richmond California
Kaiser Permanente-Roseville Roseville California
Kaiser Permanente Downtown Commons Sacramento California
Kaiser Permanente-South Sacramento Sacramento California
Kaiser Permanente-San Francisco San Francisco California
Kaiser Permanente-Santa Teresa-San Jose San Jose California
Kaiser Permanente San Leandro San Leandro California
Kaiser San Rafael-Gallinas San Rafael California
Kaiser Permanente Medical Center - Santa Clara Santa Clara California
Kaiser Permanente-Santa Rosa Santa Rosa California
Kaiser Permanente-South San Francisco South San Francisco California
Kaiser Permanente-Stockton Stockton California
Kaiser Permanente Medical Center-Vacaville Vacaville California
Kaiser Permanente-Vallejo Vallejo California
Kaiser Permanente-Walnut Creek Walnut Creek California
Epic Care Cyberknife Center Walnut Creek California
Rocky Mountain Cancer Centers-Aurora Aurora Colorado
Rocky Mountain Cancer Centers-Boulder Boulder Colorado
Rocky Mountain Cancer Centers - Centennial Centennial Colorado
Kaiser Permanente-Franklin Denver Colorado
Rocky Mountain Cancer Centers-Midtown Denver Colorado
Rocky Mountain Cancer Centers-Rose Denver Colorado
Rocky Mountain Cancer Centers - Swedish Englewood Colorado
Kaiser Permanente-Rock Creek Lafayette Colorado
Rocky Mountain Cancer Centers-Lakewood Lakewood Colorado
Rocky Mountain Cancer Centers-Littleton Littleton Colorado
Kaiser Permanente-Lone Tree Lone Tree Colorado
Rocky Mountain Cancer Centers-Sky Ridge Lone Tree Colorado

+ 226 more sites — see the full list on the official registry below.

More SWOG Cancer Research Network trials in Mexico

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04960787 on ClinicalTrials.gov ↗ ← All trials in Mexico