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1.
J Cancer Educ ; 28(2): 282-9, 2013 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-23440665

RESUMO

Racial disparities have been found in the use of chemotherapy as cancer treatment. These disparities may be, in part, due to well-documented differences in the quality of communication during clinical interactions with oncologists and Black versus White patients. In this study using a community-based participatory research approach, academic researchers, community members, and oncologists formed a partnership to develop a communication intervention to address racial disparities in cancer care. Partners developed a question prompt list (QPL), a simple tool that can be used to improve communication, and thus treatment, during clinical interactions in which oncologists and Black patients discuss chemotherapy. Partners endorsed the use of a QPL, provided specific suggestions for content and format, conducted and analyzed qualitative interviews with Black patients receiving chemotherapy, and approved the final version. The feasibility and effectiveness of the QPL that resulted from this research process are currently under evaluation in a separate study.


Assuntos
Negro ou Afro-Americano/psicologia , Comunicação , Disparidades em Assistência à Saúde/etnologia , Neoplasias/tratamento farmacológico , Neoplasias/etnologia , Educação de Pacientes como Assunto , Relações Médico-Paciente , Inquéritos e Questionários , Adulto , Idoso , Neoplasias da Mama/tratamento farmacológico , Neoplasias da Mama/etnologia , Neoplasias da Mama/psicologia , Quimioterapia Adjuvante , Neoplasias do Colo/tratamento farmacológico , Neoplasias do Colo/etnologia , Neoplasias do Colo/psicologia , Pesquisa Participativa Baseada na Comunidade , Feminino , Humanos , Entrevista Psicológica , Masculino , Pessoa de Meia-Idade , Terapia Neoadjuvante , Neoplasias/psicologia , Participação do Paciente , Satisfação do Paciente , Neoplasias Retais/tratamento farmacológico , Neoplasias Retais/etnologia , Neoplasias Retais/psicologia
2.
Trials ; 22(1): 636, 2021 Sep 17.
Artigo em Inglês | MEDLINE | ID: mdl-34535162

RESUMO

BACKGROUND: Financial toxicity, the material and psychological burden of the cost of treatment, affects 30-50% of people with cancer, even those with health insurance. The burden of treatment cost can affect treatment adherence and, ultimately, mortality. Financial toxicity is a health equity issue, disproportionately affecting patients who are racial/ethnic minorities, have lower incomes, and are < 65 years old. Patient education about treatment cost and patient-oncologist cost discussions are recommended as ways to address financial toxicity; however, research shows cost discussions occur infrequently (Altice et al. J Natl Cancer Inst 109:djw205, 2017; Schnipper et al. J Clin Oncol 34:2925-34, 2016; Zafar et al. Oncologist 18:381-90, 2013; American Cancer Society Cancer Action Network 2010). Our overall goal is to address the burden of financial toxicity and work toward health equity through a tailorable education and communication intervention, the DISCO App. The aim of this longitudinal randomized controlled trial is to test the effectiveness of the DISCO App on the outcomes in a population of economically and racially/ethnically diverse cancer patients from all age groups. METHODS: Patients diagnosed with breast, lung, colorectal, or prostate cancer at a NCI-designated comprehensive cancer center in Detroit, MI, will be randomized to one of three study arms: one usual care arm (arm 1) and two intervention arms (arms 2 and 3). All intervention patients (arms 2 and 3) will receive the DISCO App before the second interaction with their oncologist, and patients in arm 3 will receive an intervention booster. The DISCO App, presented on an iPad, includes an educational video about treatment costs, ways to manage them, and the importance of discussing them with oncologists. Patients enter socio-demographic information (e.g., employment, insurance status) and indicate their financial concerns. They then receive a tailored list of questions to consider asking their oncologist. All patients will have up to two interactions with their oncologist video recorded and complete measures at baseline, after the recorded interactions and at 1, 3, 6, and 12 months after the second interaction. Outcome measures will assess discussions of cost, communication quality, knowledge of treatment costs, self-efficacy for treatment cost management, referrals for support, short- and longer-term financial toxicity, and treatment adherence. DISCUSSION: If effective, this intervention will improve awareness of and discussions of treatment cost and alleviate the burden of financial toxicity. It may be especially helpful to groups disproportionately affected by financial toxicity, helping to achieve health equity. TRIAL REGISTRATION: ClinicalTrials.gov NCT04766190. Registered on February 23, 2021.


Assuntos
Aplicativos Móveis , Oncologistas , Neoplasias da Próstata , Idoso , Comunicação , Custos de Cuidados de Saúde , Humanos , Masculino , Ensaios Clínicos Controlados Aleatórios como Assunto , Estados Unidos
3.
Patient Educ Couns ; 103(2): 392-397, 2020 02.
Artigo em Inglês | MEDLINE | ID: mdl-31466880

RESUMO

OBJECTIVE: This study examines the preferences of patients with metastatic cancer regarding notification of imaging results, as well as distress surrounding the process. METHODS: On imaging day, preferences for notification, expectations of results, health literacy, and social support were measured. After receiving results, patients reported on actual delivery methods. At both times, patients were screened for overall distress, anxiety, and depression. RESULTS: The majority of patients preferred notification within 2 days and during a face-to-face visit with their oncologist. Although levels of distress, anxiety, and depression were low, patients with higher anxiety, depression, and social isolation had higher distress. There was no correlation between absolute distress levels and agreement between notification preferences and actual delivery methods. Receiving results from a preferred provider was associated with a decrease in distress from imaging day to follow-up. Face-to-face delivery of results was more important to people with lower health literacy. CONCLUSIONS: While distress regarding the receipt of results was low, it was higher for some groups of patients. Attending to the preferences of these subgroups may help to minimize distress. PRACTICE IMPLICATIONS: Receiving results from preferred personnel and diminishing patients' sense of social isolation might provide psychological benefit during the period surrounding imaging.


Assuntos
Diagnóstico por Imagem , Revelação/estatística & dados numéricos , Neoplasias Gastrointestinais/diagnóstico por imagem , Neoplasias Pulmonares/diagnóstico por imagem , Metástase Neoplásica/diagnóstico por imagem , Preferência do Paciente , Angústia Psicológica , Adulto , Idoso , Ansiedade , Depressão , Feminino , Neoplasias Gastrointestinais/patologia , Humanos , Neoplasias Pulmonares/patologia , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Pacientes/psicologia , Apoio Social , Tomografia Computadorizada por Raios X
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