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About
Medically under-served (i.e., low-income, uninsured, underinsured) cancer patients generally encounter significant disparities in accessing care for their mental health needs while undergoing toxic treatments that provide considerable physical and emotional stress. Thus, the investigators propose to adapt evidence-based strategies to a stepped-care intervention model to address the mental health needs of under-served lung cancer (LC) and head and neck cancer (HNC) patients and their caregivers across several levels of symptom severity (e.g., mild, moderate, or severe symptoms of depression and anxiety).
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Inclusion and exclusion criteria
LC and HNC patients:
Inclusion Criteria:
Newly diagnosed LC and/or HNC (within a month of recruitment date from the date of 1st visit oncology, Ear Nose and Throat (ENT), or radiation clinic visit/consultation upon pathologic tissue diagnosis;
LC and/or HNC patients at any stage of diagnosis (Stages 0-IV);
Over 18 years old;
English and/or Spanish speaking;
Medically underserved, as defined by at least one or several of the following:
Exclusion Criteria:
Note: Individuals who become pregnant or develop auditory impairments after they have been randomized to study condition may remain in the study until completion.
Caregivers of LC and/or HNC patients
Inclusion Criteria:
Primary caregiver of a newly diagnosed LC and/or HNC patient (per criteria for patients);
Over 18 years old;
English and/or Spanish speaking;
Medically underserved, as defined by at least one or several of the following:
(c.1) Public insurance (i.e., Medicaid, Medicare exclusive, VA);
(c.2) 10% of annual income spent on out-of-pocket medical expenses for individuals below 200% of the 2016 Federal poverty level.
Exclusion criteria:
Individuals who do not meet eligibility criteria, including individuals who do not speak English or Spanish [at the discretion of the Site Coordinators upon recruitment];
Caregivers of patients who refuse treatment at one of three hospital sites.
Decisionally challenged adults with:
Individuals from:
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535 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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