Frances R. Nedjat-Haiem
University of Southern California
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Publication
Featured researches published by Frances R. Nedjat-Haiem.
Cancer | 2008
Kathleen Ell; Bin Xie; Anjanette Wells; Frances R. Nedjat-Haiem; Pey-Jiuan Lee; Betsy Vourlekis
Attention to the economic consequences of cancer has grown as the number of cancer survivors is increasing. Although prevalent among low‐income minority survivors, the impact of economic stress on quality of life (QOL) remains largely unexplored.
Cancer | 2009
Kathleen Ell; Betsy Vourlekis; Bin Xie; Frances R. Nedjat-Haiem; Pey-Jiuan Lee; Laila I. Muderspach; Christy A. Russell; Lawrence A. Palinkas
The authors implemented a controlled, randomized trial that compared 2 interventions: the provision of written resource navigation information (enhanced usual care [EUC]) versus written information plus patient navigation (TPN) aimed at improving adjuvant treatment adherence and follow‐up among 487 low‐income, predominantly Hispanic women with breast cancer or gynecologic cancer.
Supportive Care in Cancer | 2012
Frances R. Nedjat-Haiem; Iraida V. Carrion; Kathleen Ell; Lawrence A. Palinkas
ObjectivePrevious cancer research does not adequately inform us about the experiences of managing a more serious, life-threatening cancer condition, especially for underserved Latinas. This study was designed to explore the ways in which Latinas navigate through and deal with advanced cancers.MethodsA purposive sample of 24 underserved Latina women was selected from a randomized controlled trial. Data were analyzed using a phenomenological approach to explore navigation of the advanced cancer experience.ResultsThis study outlines a conceptual framework which denotes the interconnectedness of multiple factors that influence the cancer experience for Latina women. Experiences with advanced cancer were embedded within a social, cultural, and systemic framework described as 1) intrapersonal experiences; 2) interpersonal experiences; 3) provider interactions; and 4) medical system factors.ConclusionsThis study indicates that underserved Latinas face complex circumstances that interfere with the diagnosis and treatment of cancer. However, women expressed positive attitudes and held beliefs about survival which helped them through their experience with cancer. The implication of these findings is that Latinas have protective attitudes and beliefs that help them to overcome “tragic” circumstances. Providers need to become aware of the complexity of these issues in order to achieve competent, effective, and efficient practice in medical settings with Latinas.
American Journal of Hospice and Palliative Medicine | 2013
Iraida V. Carrion; Frances R. Nedjat-Haiem
This study examined the various settings in which caregiving occurred for terminally ill older Latinos. Qualitative data were collected in Central Florida through in-depth, semi-structured, open-ended interviews. 20 Latinos caring for terminally ill Latinos participated in the study. N = 9 Latino family (unpaid) caregivers provided care in the terminally ill persons home, while N = 4 provided care to a family member in the caregivers home. N = 4 paid caregivers provided care to terminally ill Latinos who reside in the caregivers private home and N = 3 in an assisted-living facility. The themes indicate that family (unpaid) caregivers experienced changes in their financial status; they both encountered English language barriers. Geographical distance made caregiving more challenging. Paid caregivers adapted to cultural expectations and their higher income enabled them to hire assistance.
American Journal of Hospice and Palliative Medicine | 2015
Frances R. Nedjat-Haiem; Iraida V. Carrion
Multiple factors influence end-of-life (EOL) care discussions that occur in health care systems, within organizations, among individuals working within these systems and in patients and family/friend support networks. This study examined barriers to EOL care discussions as experienced by health care providers working in a public safety-net health care system where the majority of their patients were low-income and immigrant Latinos seeking medical treatment. Qualitative data were collected in South Central Los Angeles through semistructured interviews with 46 health care providers from different disciplines in medicine, nursing, social work, and chaplaincy. The themes indicated communication barriers in the public sector health care setting and sociocultural patient- and family-level factors. All providers made valuable contributions to clarify the complexity of the problems. Universal strategies are needed to improve communication.
Journal of Cancer Education | 2013
Iraida V. Carrion; Frances R. Nedjat-Haiem; David X. Marquez
Journal of Pain and Symptom Management | 2012
Frances R. Nedjat-Haiem; Karl A. Lorenz; Kathleen Ell; Alison B. Hamilton; Lawrence A. Palinkas
Supportive Care in Cancer | 2013
Iraida V. Carrion; Frances R. Nedjat-Haiem; Dinorah Martinez-Tyson; Heide Castañeda
Social Work in Health Care | 2013
Frances R. Nedjat-Haiem; Iraida V. Carrion; Kristen Cribbs; Karl A. Lorenz
Omega-journal of Death and Dying | 2013
Frances R. Nedjat-Haiem; Iraida V. Carrion; Karl A. Lorenz; Kathleen Ell; Lawrence A. Palinkas