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a note will indicate the deletion.
UMI 3394179
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Dedication
I dedicate this dissertation to my partner, William D. Corbin and my parents, Henry R.
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Acknowledgments
I express my appreciation to the members of my dissertation committee. I thank
Dr. Susan C. McMillan, Committee Chair, for her encouragement, generosity,
unwavering support, advice, kindness and understanding throughout my academic
endeavors at the College of Nursing at the University of South Florida. I thank Dr. Lois
O. Gonzalez, Dr. Versie Mallard-Johnson and Dr. Brent Small for their advice, comments
and support during this process.
I thank Dr. Janine Overcash for the experience of working with her on studies and
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my growth as a new researcher. I thank Rod Hale of the Graduate School for his
Table of Contents
List of Tables ................................................................................................................ iv
List of Figures ................................................................................................................. v
Abstract ......... ................................................................................................................ vi
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Hypothesis 2 ........................................................................................ 23
Hypothesis 3 ........................................................................................ 23
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iii
List of Tables
Demographic Characteristics .................................................................. 32
Table 2
Table 3
Table 4
Table 5
Table 6
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Table 7
Table 1
iv
List of Figures
McMillans Modified Emanuel and Emanuel (1998)
Model for a Peaceful Death .................................................................... 20
Figure 2
Figure 3
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Figure 1
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cancer caregiver depression symptomatology. The purpose of the study was to examine
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vii
CHAPTER ONE
INTRODUCTION
Chronically ill and end of life patients are increasingly being cared for in the
home by family, friends, or neighbors. These individuals are referred to as informal or
voluntary caregivers. They are not professionally trained for the caregiving role and are
not financially compensated. More than 44 million individuals in the United States each
year are voluntary primary caregivers for a chronically ill, disabled or aged family
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member or friend, with the value of their services estimated at 306 billion dollars each
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While the duration of the cancer illness may be shorter than that of other serious
diseases, such as dementia, caregivers of cancer patients provide many more hours of
care during a week (Haley, Lamonde, Han, Narramore, & Schonwetter, 2001).
Caregivers for end of life patients are subjected to an intense caregiving experience for
which they may not have been adequately prepared or expected. Identifying caregivers at
risk for depression symptomatology is particularly important in this patient population.
This is necessary not only for the physical and emotional health of the caregiver, but also
that of the cancer patient whose quality of life and care may be adversely affected.
Quality of care and life is particularly critical for patients at the end of life.
While research has found a relationship between caregiving and depression, a
search of the literature revealed that studies of predictors of depression symptoms in
caregivers of cancer patients at the end of life are sparse. A small study of 51 caregivers
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of patients with advanced cancer, recruited from ambulatory clinics, focused on caregiver
sleep as a predictor of caregiver depression symptoms (Carter & Chang, 2000). There are
also limited studies of caregivers of cancer patients in the hospice setting. A study
comparing dementia and cancer caregivers of hospice patients had a small sample size
and was limited to only spousal caregivers (Haley et al., 2001). Further research directed
at the intensive experience of caregiving of hospice cancer patients and caregiver
depression symptomatology is needed, due to limited research on this particular
caregiving experience. There is a need to assess caregivers for depression symptoms and
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symptomatology can be used to improve the psychological and mental health of informal
caregivers, improve their quality of life and ensure quality care for those in need.
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Problem Statement
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financially compensated to render care and who provides at least four hours of care a day.
Depression Symptomatology
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(Vitaliano et al., 2002; Sherwood et al. 2004; Ferketich, Schwartzbaum, Frid, &
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mortality rate in caregivers (Schulz & Beach, 1999). Caregiving has significant negative
effect on cells of the immune system, including T cells and natural killer cells (Pariante et
al., 1997; Scanlan, Vitaliano, Zhang, Savage, & Ochs, 2001; Vitaliano et al., 1998). In
addition to effects at the cellular level, caregivers have increased levels of coronary heart
disease (CHD) and metabolic syndrome when compared to noncaregivers (Vitaliano et
al).