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Thematische Bibliographien / Caregivers / Dissertationen

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Dissertationen zum Thema „Caregivers“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 25. Juli 2025

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1

Kaushik, Sanjana. "Social Networks of Technology Caregivers and Caregivees." University of Cincinnati / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1613749933487134.

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2

Nauser, Julie Ann. "Heart failure family caregivers psychometrics of a new quality of life scale and variables associated with caregiver outcomes /." Connect to resource online, 2007. http://hdl.handle.net/1805/1139.

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Thesis (Ph.D.)--Indiana University, 2007.<br>Title from screen (viewed on September 21, 2007). School of Nursing, Indiana University-Purdue University Indianapolis (IUPUI). Advisor(s): Tamilyn Bakas, Sharon Sims, Mary L. Fisher, Janet Welch. Includes vitae. Includes bibliographical references (leaves 228-244).

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3

Kum, Cleopatra Eghem. "Theoretically Based Factors Affecting Health in Stroke Family Caregivers." University of Cincinnati / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1627660913055465.

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4

Kimemia, Veronica. "CAREGIVER BURDEN AND COPING RESPONSES FOR FEMALES WHO ARE THE PRIMARY CAREGIVER FOR A FAMILY MEMBER LIVING WITH HIV/AIDS IN KENY." Doctoral diss., University of Central Florida, 2006. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/2682.

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Caring for a family member who is ill can be a draining experience (Cooper et al., 2006; Daire, 2002; Zarit et al, 1980). Providing care for a family member that is living with HIV/AIDS is potentially even more stressful because of social meanings associated with HIV/AIDS infection (Stajduhar, 1998) and the contagious nature of the HIV virus (Powell-Cope & Brown, 1992). Research indicates that most caregivers are female (Bunting, 2001; Songwathana, 2000). In Africa women bear the brunt of the burden of providing care for family members who are living with HIV/AIDS (Mushonga, 2001; Olenja, 1999

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5

Demirtepe, Dilek. "Testing The Caregiver Stress Model With The Caregivers Of Children With Leukemia." Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/12609327/index.pdf.

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The aim of the present study was to investigate the relationship between the stressors of the caregiving process and the health related outcomes (depression, anxiety, and general psychological health) in caregivers of children with leukemia. Caregiver Stress Model was used as the conceptual framework for the study. In order to measure the stressors of the caregivers, caregiver well-being scale was adapted to Turkish culture as the study 1 by using the caregivers of family members with various chronic illnesses. The analyses showed that Turkish version of the caregiver well-being scale had sati

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6

Konag, Ozlem. "Testing The Caregiver Stress Model With The Primary Caregivers Of Schizophrenic Patients." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613797/index.pdf.

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The aim of this study was to examine the relationship between the stressors of caregiving for a schizophrenic patient and related outcomes. The Caregiver Stress Model was used as the conceptual framework for the current study. The sample of the study was composed of 98 Turkish caregivers of schizophrenic patients who were treated at psychiatry clinics of hospitals in Ankara. Twelve mediation models were tested using marital satisfaction and social support as mediators. The models contained primary stressor (basic needs), secondary stressor (activities of living), and intrapsychic strain (paren

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7

Coolbear, Jennifer. "Caregiver-infant interactions and caregivers' representations of relationships in failure to thrive." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ56222.pdf.

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8

Salinas, Maureen R. "Caregiver Burden and Depressive Symptoms in Hispanic Caregivers of Alzheimer's Disease Patients." Scholarship @ Claremont, 2016. http://scholarship.claremont.edu/scripps_theses/795.

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Caregiving for a close family member with Alzheimer’s disease is a stressful situation to be in, that often leads to high levels of caregiver burden and subsequent stress and depressive symptoms, and while there are numerous community and government resources available to caregivers, there are aspects of Hispanic cultures that may lead Hispanic caregivers to have higher levels of caregiver burden and depressive symptoms than White caregivers. 80 Hispanic caregivers and 80 White caregivers, with 40 males and 40 females within each group, will be recruited to participate in this study. Scales wi

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9

King, Jennifer Kay. "Caregiving Style in Diverse Samples of Caregivers." Thesis, University of North Texas, 2006. https://digital.library.unt.edu/ark:/67531/metadc5363/.

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With three homogenous caregiver groups (i.e., Alzheimer's caregivers, grandparents raising grandchildren, parents), caregiving styles were explored to determine their reliability and validity, their unique role in predicting caregiver outcomes, and their differences between groups of caregivers. A conceptual framework was adapted to determine the impact of contextual variables, caregiving styles, caregiver appraisal, and mediating variables on caregiving outcomes. A more concise version of the Caregiving Style Scale (CSS) was developed with 49 items yielding an internal consistency coefficient

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Patel, Bina Ranjit. "A Mixed Methods Inquiry of Caregivers of Veterans with Sustained Serious "Invisible" Injuries in Iraq and/or Afghanistan." Scholar Commons, 2016. http://scholarcommons.usf.edu/etd/6562.

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Currently, there are approximately 1.1 million caregivers who are caring for veterans who have served in the military following September 11 (9/11), 2001 (Ramchand et al., 2014). In this study, a mixed methods analysis of post 9/11 caregivers enrolled in the North Florida South Georgia Caregiver Support Program was completed with a convenience sample of 172 participants for quantitative analysis which included 16 participants for the phenomenological query. Correlations, t-tests, and ANOVAs were used to determine the associations among race, gender, age, caregiver type, diagnosis, tier level,

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Clements, Linda. "CAREGIVERS’ INFLUENCE ON PATIENTS’ HEART FAILURE SELF-CARE, HOSPITAL READMISSION AND MORTALITY." UKnowledge, 2019. https://uknowledge.uky.edu/nursing_etds/48.

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Background: Heart failure (HF) is a leading cause of hospitalization, readmissions, and death in the United States. Patients hospitalized for HF are at risk for readmission, in- hospital mortality, and early post-discharge death. In the United States, inpatient care has been estimated to cost $83,980 over the lifetime of each patient with HF. The majority of patients with HF depend on caregiver support for successful HF self-care, which is essential for optimal patient outcomes. Support from caregivers is thought to be important for better self-care, and lower readmission and mortality rates.

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12

Weierbach, Florence M. "Health Caregivers Workshop." Digital Commons @ East Tennessee State University, 2012. https://dc.etsu.edu/etsu-works/7405.

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13

Amini, Pay Noura. "Patient handling activities by informal caregivers: Informal caregiver’s biomechanical loads during patient repositioning." The Ohio State University, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1563462946325851.

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14

Glaze, Joy Adella. "The Lived Experiences of Caregivers of Lung Transplant Recipients." FIU Digital Commons, 2018. https://digitalcommons.fiu.edu/etd/3683.

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Lung transplantation is a treatment for patients with end stage lung disease; they will not survive without such surgery. A caregiver is essential for a patient to become eligible for a lung transplant and the caregiver plays an essential role in the transplant recipient’s care both before and after transplant surgery. Most caregiver research has been conducted on caregivers of persons with Alzheimer’s disease, dementia or on elderly patients, however, it is important to examine caregivers’ experiences caring for other patient groups with disabling conditions. Caregivers of transplant recipien

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Plange-Kaye, Elizaebth. "Caregivers' Burden| A Phenomenological Study of the Lived Experiences of Informal Caregivers." Thesis, University of Phoenix, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10744463.

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<p>ABSTRACT The current increase in the population of older adults has created a high demand for more informal caregivers. Informal caregivers complain of many problems in providing care including psychological stresses and anxieties, as well as physical, emotional, financial, and other social burdens. The purpose of this phenomenological study was to understand and describe the essence of the lived experiences of informal caregivers. The study was also intended to make health professionals and policy makers aware of such problems. The study adopted a qualitative methodology and a hermeneutica

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Stacy, Kelly E. "Needs and Concerns of Family Caregivers of Persons with Lewy Body Disease (LBD)." University of Cincinnati / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1627663824224801.

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17

Sawyer, Mary Rachel. "Caregiver Training: Increasing Generalization of Parenting Skills Through Teaching Caregivers to Recognize Child Behavior." Scholar Commons, 2012. http://scholarcommons.usf.edu/etd/4220.

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Previous research has demonstrated the efficacy of a behavioral parent training program for increasing the accuracy of trained skills; however, few studies have examined the extent to which those skills generalize to the natural environment (i.e., the home) and are used with the target individual (i.e., the child). In addition, little is known about the direct effect that caregiver implementation of the skills has on child behavior. A multiple baseline across participants design was used to (a) assess caregiver accuracy with implementation of three parenting skills, and (b) assess subsequent e

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18

Kietzman, Kathryn Gail. "A reason to care motivation to assume a paid caregiver role and correlates of well-being among family members and friends /." Diss., Restricted to subscribing institutions, 2008. http://proquest.umi.com/pqdweb?did=1666115091&sid=3&Fmt=2&clientId=1564&RQT=309&VName=PQD.

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19

Lezotte, Edna Mae. "Use of religious and spiritual resources as a means of self care for coping with vicarious traumatization." Theological Research Exchange Network (TREN), 2000. http://www.tren.com.

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20

Clear, Mike. "Public discourse personal reality : disablement and a re-search for caring culture /." View thesis View thesis, 1996. http://library.uws.edu.au/adt-NUWS/public/adt-NUWS20030529.110649/index.html.

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Thesis (PhD. Philiosophy)--University of Western Sydney, Hawkesbury, 1996.<br>"This thesis is presented for the degree of Doctor of Philosophy, University of Western Sydney, 1996." Includes bibliographical references (p. 288-306).

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21

Hamdy, Ronald C., J. V. Lewis, Rebecca Copeland, et al. "Repetitive Questioning Exasperates Caregivers." Digital Commons @ East Tennessee State University, 2018. https://dc.etsu.edu/etsu-works/2739.

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Repetitive questioning is due to an impaired episodic memory and is a frequent, often presenting, problem in patients with Alzheimer’s disease (amnestic type). It is due to the patients’ difficulties learning new information, retaining it, and recalling it, and is often aggravated by a poor attention span and easy distractibility. A number of factors may trigger and maintain repetitive questioning. Caregivers should try to identify and address these triggers. In the case discussion presented, it is due to the patient’s concerns about her and her family’s safety triggered by watching a particul

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22

Anderson, Cristina L. (Cristina Lee). "Caregiver Personality as a Contributing Factor in Caregiver Burden." Thesis, University of North Texas, 1994. https://digital.library.unt.edu/ark:/67531/metadc500270/.

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Personality characteristics of spousal and adult children and active potential caregivers of persons with Alzheimer's Disease were studied in order to better predict caregiver burden and aspects of well-being. Contrary to prediction, no differences were found between spouse and adult children active caregivers on measures of well-being. Additionally, adult children potential caregivers indicated feeling less control over their lives than spouse potential caregivers. When social desirability was controlled, active caregivers reported greater fluctuations in affect than did potential caregivers.

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Slade, Rebecca. "Examination of dementia caregivers' experiences : the role of suffering and empathy in the caregiving relationship and a review of the evidence base for interventions targeting caregiver anxiety." Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/33301.

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Background: Dementia, which affects an estimated 35 million individuals worldwide, is now recognised as a growing health and economic problem. With insufficient levels of health and welfare services in many nations, there exists a reliance on family caregivers to provide care for individuals with dementia (IWDs). However, the potential negative psychological and physical consequences of the caregiving role cannot be ignored. A growing literature base has improved the theoretical understanding of mental health difficulties (e.g. depression, burden) in caregivers. However, significant gaps in th

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McBride, Sara. "Understanding the cognitive processes of problem detection and decision making among assisted living caregivers." Diss., Georgia Institute of Technology, 2014. http://hdl.handle.net/1853/51797.

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It is estimated that by 2050 the proportion of older adults in the U.S. will reach 20% (U.S. Census Bureau, 2008). This increase in the elderly population will likely be associated with a greater need for supportive services in various sectors, including healthcare and housing, such as assisted living communities. Many older adults choose to reside in assisted living communities due to increased difficulty managing health conditions or performing activities of daily living (e.g., bathing, toileting, walking). A primary goal of assisted living communities is to help residents maintain their hea

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25

Miller, Meagan. "Claiming a life of permanence: Filipina caregivers' migration experiences in Canada's live-in caregiver program." Thesis, McGill University, 2011. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=96836.

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Drawing on in-depth interviews with migrant caregivers, community workers and government employees, this thesis explores the dream among Filipina women working in Canada's Live-In Caregiver Program (LCP) to build a life in Canada. Uncovering the actions they take on the path to realizing this dream, I first examine the common challenges caregivers encounter while working as temporary workers in the LCP. The analysis deepens to reveal the struggles caregivers engage in to improve their lives, despite institutional obstacles to exercising their rights. Ultimately, the analysis addresses the wide

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McEwen, Marylyn. "Family adaptability, family cohesion, spirituality and caregiver strain in women as caregivers of elder kin." Thesis, The University of Arizona, 1987. http://hdl.handle.net/10150/558069.

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27

VanMeter, Adrianna J. "The Impact of Dementia Caregiving on Caregiver Cognitive Health." Ohio University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1508854228522232.

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28

Williams, Elizabeth A. "Caregiving Burden and Heart Rate Variability: Differences by Race and Gender." Case Western Reserve University School of Graduate Studies / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1586291354640556.

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29

Halpern, Michael T., Mallorie H. Fiero, and Melanie L. Bell. "Impact of caregiver activities and social supports on multidimensional caregiver burden: analyses from nationally-representative surveys of cancer patients and their caregivers." SPRINGER, 2017. http://hdl.handle.net/10150/626018.

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Informal caregivers of individuals with cancer may experience substantial burdens. To develop interventions to support these caregivers, it is crucial to quantify and understand the domains of burdens potentially experienced by caregivers and factors contributing to each domain. Using data from two national surveys, the National Survey of Caregiving (NSOC) linked to the National Health and Aging Trends Survey (NHATS), we identified all participants in the NHATS diagnosed with cancer who had a caregiver participating in the NSOC. Guided by a theoretical model, twenty-two items in the NSOC relat

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Zerth, Erin O. "Applying a manualized intervention for rural caregivers to caregivers of older medical rehabilitation patients /." Available to subscribers only, 2008. http://proquest.umi.com/pqdweb?did=1594477041&sid=10&Fmt=2&clientId=1509&RQT=309&VName=PQD.

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31

Holroyd, Eleanor Anne. "Chinese family caregivers : dilemmas at the extremity of public and private obligations /." Thesis, Hong Kong : University of Hong Kong, 1998. http://sunzi.lib.hku.hk/hkuto/record.jsp?B20715353.

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32

Dick, Suzanne. "The needs of informal caregivers." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/mq23276.pdf.

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33

Wolff, Megan, Kelly Daniel, Julia Najm, and Diana PhD Morelen. "Taking Care of the Caregivers." Digital Commons @ East Tennessee State University, 2021. https://dc.etsu.edu/asrf/2021/presentations/32.

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The present study examined the impact of COVID-related stress on the mental health and professional burnout in the infant and early childhood mental health (IECMH) workforce and to examine reflective supervision and consultation (RSC) as a possible protective factor that buffers against the detrimental impact of COVID-related stress. Participants included 123 adults (n = 121 female, modal age range 30-39 years) in the TN IECMH workforce (mean years of experience = 13.6 years) surveyed in June/July 2020. Sector representation was quite varied (home-visiting, childcare, child welfare, early int

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Spearman, Marilyn S. "The expressions of male caregivers /." The Ohio State University, 1999. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487952208105824.

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35

Nunez, Guero. "BELIEFS ABOUT RESPITE AMONG CAREGIVERS." CSUSB ScholarWorks, 2016. https://scholarworks.lib.csusb.edu/etd/298.

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The emphasis of this research was to evaluate the beliefs about respite among caregivers of the clients associated with Inland Caregiver Resource Center. The caregivers of the elderly and those who suffer from Alzheimer’s and dementia, or suffer from traumatic brain injury that was organic in nature were the population of interest. These caregivers were unpaid persons who help to keep those with such conditions at home as long as possible. This study used an exploratory pilot survey instrument to assess the perception of benefit of respite used as seen from the view of the caregiver. The prima

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Gideon, Clare A. "SOCIAL ENVIRONMENTS OF DEMENTIA CAREGIVERS: RELATIONSHIPS BETWEEN SOCIAL SUPPORT, NEGATIVE SOCIAL INTERACTIONS, AND CAREGIVER EMOTIONAL DISTRESS." online version, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=case1158541315.

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37

Zhao, Yuxin. "Exploring the Effect of Caregiver Burden among Alzheimer's Caregivers: A Test of The Stress Process Model." Thesis, Virginia Tech, 2019. http://hdl.handle.net/10919/86840.

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The diagnosis of Alzheimer's disease (AD) is stressful for both patients and their family caregivers (FCG). As the disease progresses, the patient's memory, functioning status, and behavioral problems get worse, and the needs of the patient that must be addressed by family caregivers increase dramatically. This research examines the impact of the subjective burden with the objective stressors on FCG's depression and to determines which psychosocial resources can be used to either mediate or moderate this relationship. I examine the baseline data that was collected from 670 family caregivers o

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Lee, Jaime. "Why Technology for Caregivers Fail| A Qualitative Study of GPS-Based Technology Supporting Alzheimer's Caregivers." Thesis, University of Baltimore, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10746907.

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<p> The purpose of this research is to understand the usability challenges of wearable Global Positioning System (GPS)-based technologies for at home caregivers managing wandering effects for loved ones with Dementia, specifically those with Alzheimer's disease. A total of four devices and 14 U.S. participants were studied using semi-structured, in-person qualitative usability methodology and an open coding system in the style of Grounded Theory. Though the study evaluated issues solely related to usability, the results expanded to a much larger design paradigm to be considered for improved an

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Cornu, Matthew. "CAREGIVERS OF PARENTS WITH AlZHEIMER’S DISEASE: QUALITY OF LIFE FOR CAREGIVERS: PERSPECTIVES & FAMILY DYNAMICS." UKnowledge, 2019. https://uknowledge.uky.edu/hes_etds/75.

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This study furthers Alzheimer’s family literature regarding the impact of caregiver attachment, readiness to provide care, and caregiver quality of life. A sample of 33 participants caring for a parent with Alzheimer’s disease in the state of Kentucky was recruited to complete a questionnaire for the study. The questionnaire consisted of an online survey about participants’ experiences and attachments growing up with their parents, their experiences becoming caregivers to their parents with Alzheimer’s disease, and participants’ current perspectives of their own quality of life. Positive persp

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Stebbins, Peter. "Predictors of psychological distress in caregivers of people with acquired brain injury : a cognitive behavioural analysis /." [St. Lucia, Qld.], 2005. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe19107.pdf.

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Simmons, Barbara. "Perceptions of Well-being and Coping Mechanisms from Caregivers of Individuals with Autism." ScholarWorks, 2019. https://scholarworks.waldenu.edu/dissertations/6671.

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Caregivers of individuals with autism often report increased levels of stress and a lack of social support to help them cope with various stressors as they provide care. Without coping mechanisms or social support, as individuals with autism present various behavioral and emotional challenges, caregivers can experience a decline in well-being. Thus, the purpose of this qualitative study was to explore the processes that caregivers of individuals between the ages of 9-18 diagnosed with autism use to cope with stress and social support in Southeast Georgia. Grounded theory was used to describe t

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Taylor, Karen Jackqueline. "Impacting the awareness of God's presence within the challenges of giving full time care to one diagnosed with Alzheimer's disease." Theological Research Exchange Network (TREN), 2007. http://www.tren.com/search.cfm?p028-0274.

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Ng, Ka-man Carmen. "An exploration of experiential learning with carers participating in a multi-skills training course on care of the elderly." Hong Kong : University of Hong Kong, 2000. http://sunzi.lib.hku.hk/hkuto/record.jsp?B22331463.

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Koumoutzis, Athena N. "Age Differences in Stressors and Outcomes Among Young Adult, Midlife, and Older Adult Caregivers." Kent State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=kent1553839757877709.

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Aguirre, Monique LaShone. "Social Support, Psychological Distress, and Behavioral Outcomes Among Palliative Care Caregivers." ScholarWorks, 2018. https://scholarworks.waldenu.edu/dissertations/6159.

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Social support and acute care facility providers need information about how to help improve the practices and knowledge of caregivers related to the stages of palliative care. The purpose of this study was to examine whether there was a significant association between social support and psychological distress and behavioral outcomes among palliative care caregivers, and to determine to what extent social support buffered psychological distress and behavioral outcomes. The quality-of-life model guided the study. The study used a quantitative cross-sectional research design with secondary data a

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Price, Katey A. "Aphasia and the identity of Alzheimer’s family caregivers: The effect of communication ability on caregiver identity gaps." The Ohio State University, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=osu1387538328.

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47

Alva, Jessica Isabel. "Family Caregiver Interdependence: A Dyadic Analysis of Primary and Secondary Caregivers of Relatives with Major Neurocognitive Disorder." Case Western Reserve University School of Graduate Studies / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=case1465660522.

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48

Bryant, Jonanna R. "Characteristics of the Informal Caregiver: An Integrative Literature Review." ScholarWorks, 2016. https://scholarworks.waldenu.edu/dissertations/2397.

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The needs of the informal caregiver can be difficult to determine apart from those related to caring for the terminally ill loved one. Often, informal caregivers' individual needs are lost because of their day-to-day responsibility and care of their terminally ill loved one. The purpose of this project was to discover the characteristics of informal caregivers of the terminally ill. An integrated literature review was conducted using the Fineout-Overhalt, Melnyk, Stillwell, and Williamson's (2010) analytical approach to reviewing the evidence. The approach consisted of 7 levels for evaluating

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Waterfall, A. Christine. "Needs of caregivers of stroke survivors." Virtual Press, 2002. http://liblink.bsu.edu/uhtbin/catkey/1246469.

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Stroke is a medical event that has serious consequences for the survivor, his family, and society. Stroke is the third leading cause of death in the United States, and two-thirds of stroke survivors are permanently disabled with one-half of these survivors considered severely impaired. The economic burden from stroke is estimated to be $30 billion annually in health care costs and lost productivity.This study described the needs of 35 caregivers of stroke survivors within 24 hours of discharge to home from an acute care "safety net" teaching hospital in Indiana and how well those needs were me

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Anyabolu, Oliver Ifeanyi. "Understanding Caregivers' Perceptions of Childhood Immunization." Thesis, Walden University, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10180866.

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<p> Low immunization in Nigeria is associated with high prevalence of childhood diseases. The purpose of this qualitative phenomenological study was to describe caregivers’ perceptions of routine immunization of their children ages 24 to 36 months. Caregivers’ attitudes, cultural beliefs, and knowledge regarding immunization were examined. The health belief model was used to guide study. Interviews were conducted with 5 caregivers of fully immunized and 5 caregivers of partially and nonimmunized children. Digital recordings were analyzed using NVivo 10 to identify themes and subthe

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