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Dissertations / Theses on the topic 'Caregivers Care of the sick'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 February 2022

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1

Graf, Theresa M. "Sense of coherence, relational functioning and concepts of health in adult daughter caregivers as compared with an age cohort of women /." Access Digital Full Text version, 1994. http://pocketknowledge.tc.columbia.edu/home.php/bybib/11625235.

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Thesis (Ed.D.)--Teachers College, Columbia University, 1994.<br>Includes tables and appendices. Typescript; issued also on microfilm. Sponsor: Marilyn Rawnsley. Dissertation Committee: Jane A. Monroe. Includes bibliographical references (leaves 117-131).

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2

Babbage, Roberta Louise. "Relieving strain in informal caregivers of the elderly." CSUSB ScholarWorks, 1989. https://scholarworks.lib.csusb.edu/etd-project/459.

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3

De, Boever Dave. "Being a caregiver to people living with AIDS stages on the journey /." Theological Research Exchange Network (TREN), 1991. http://www.tren.com.

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4

Downes, Edith A. "Spiritual companions for Alzheimers patients and those persons with other forms of dementia." Online full text .pdf document, available to Fuller patrons only, 2002. http://www.tren.com.

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5

Burt, John. "How to minister to individuals with family members in personal care homes." Online full text .pdf document, available to Fuller patrons only, 2002. http://www.tren.com.

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6

Mentzakis, Emmanouil. "Economic issues of informal care values and determinants /." Thesis, Available from the University of Aberdeen Library and Historic Collections Digital Resources, 2008. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=25213.

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7

Amonette, J. Fulton. "The establishment of a care team of trained volunteers from Northwest Baptist Church of Miami, Oklahoma, to serve homebound senior adults and their caregivers." Online full text .pdf document, available to Fuller patrons only, 2004. http://www.tren.com.

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Ministry research project (D. Min.)--Midwestern Baptist Theological Seminary, 2004.<br>Submitted in partial fulfillment of the requirements for the Doctor of Ministry Degree. Includes bibliographical references (leaves 220-225).

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8

Scannell, Alice Updike. "The Longterm Psychosocial Impacts of Caregiving on the Caregivers of Persons with Stroke." PDXScholar, 1989. https://pdxscholar.library.pdx.edu/open_access_etds/1312.

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This study is a Time 4 (T4) follow-up interview of ninety-three caregivers of persons who experienced a first stroke between 2 to 4 years (mean = 36 months) prior to the T4 interview. The first wave of data collection occurred within two months after the stroke. The second and third waves occurred six and twelve months, respectively, after the first interview. The caregivers were identified by the person with stroke as being the person closest to him/her who would be responsible for care after the stroke. Data were gathered at all four interviews using reliable and valid measures for depressiv

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9

Munro, Ian. "The lived experience of gay men caring for others with HIV/AIDS living, loving, and dying in the era of HIV/AIDS /." Connect to this title online, 2002. http://tux.lib.deakin.edu.au/adt-VDU/public/adt-VDU20020913.150027/.

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10

Risco, Vilarasau Ester. "La transició de l’atenció sociosanitària de les persones amb demència i dels seus cuidadors." Doctoral thesis, Universitat de Barcelona, 2015. http://hdl.handle.net/10803/399679.

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INTRODUCCIÓ: Per tal de dissenyar noves estratègies per estabilitzar la situació de les persones que tenen un diagnòstic de demència i que viuen en el domicili, s'ha desenvolupat un estudi que descriu l’entorn de la transició des del domicili fins a una institució de llarga en persones grans amb demència i dels seus cuidadors. METODOLOGIA: Aquesta investigació s'ha realitzat en dues etapes. En la primera etapa es compara, a nivell europeu, la reacció dels cuidadors informals en la demència, els nivells d’associació de la dependència i els símptomes neuropsiquiàtrics amb la institucion

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11

Irazábal, Giménez Marcia. "Carga e impacto familiar de las cuidadoras y los cuidadores de personas adultas con discapacidad intelectual con o sin trastorno mental asociado." Doctoral thesis, Universitat de Barcelona, 2017. http://hdl.handle.net/10803/461006.

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La relevancia e interés por el estudio sobre la carga familiar y el impacto familiar del cuidado de personas adultas con discapacidad intelectual (DI) y discapacidad intelectual con trastorno mental asociado (DI-TM) ha aumentado durante las últimas dos décadas en España. Sin embargo, dicha temática apenas ha sido investigada en nuestro país. La presente investigación pretende contribuir al conocimiento sobre estas áreas, y tiene por finalidad analizar los principales factores sociales y psicológicos, así como las variables clínicas y diagnósticas que explican mayores niveles de carga e impacto

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12

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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13

Rennie, Claire Marie. "The care of sick children in eighteenth-century England." Thesis, University of Leeds, 2016. http://etheses.whiterose.ac.uk/16508/.

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This thesis develops our understanding of childhood illness and care through an examination of the types of care which were provided to children who suffered from common diseases and conditions in the eighteenth century. My research establishes that domestic care remained the norm throughout the eighteenth century, even though institutional care grew both in terms of its scope and the numbers treated in this period. This study reveals that Newton’s concept of ‘children’s physic’ retained its importance in the domestic setting. The development of institutions did not radically change the manner

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14

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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15

Wolfe, Phillips Emily. "Promoting Self-Care Behaviours Among Cancer Caregivers." Thesis, Université d'Ottawa / University of Ottawa, 2021. http://hdl.handle.net/10393/41847.

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Caregivers play an integral role in the cancer care system in Canada as they provide unpaid care and support for millions of adults living with and beyond cancer. Although caregiving can be a positive experience for some, assuming a caregiving role can be detrimental to caregivers’ own physical and mental health. Research over the past decade has highlighted the negative impacts of caregiving and called for more efforts focused on improving caregivers’ wellbeing. Most interventions targeting caregivers are largely designed to support them in providing care, with little emphasis placed on speci

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16

Landon, Kelly S. (Kelly Suzanne) Carleton University Dissertation Sociology and Anthropology. "Caregivers take care! A literary anthology of journey toward shared care." Ottawa, 2000.

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17

Duncan, Marie Theresa. "Alzheimer's Disease Caregivers: The Transition from Home Care to Formal Care." PDXScholar, 1992. https://pdxscholar.library.pdx.edu/open_access_etds/3228.

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When family members no longer have the capacity to meet Alzheimer's Disease (AD) caregiving demands at home, a move to a nursing home or other formal care facility becomes the only solution. Recognizing this as a time of transition, three research questions were identified: (1) What do family caregivers to AD individuals experience as they shift their caregiving from home to formal care settings? (2) How does caregiving in formal care differ from caregiving at home? and (3) How do family caregivers perceive the relationships that develop between families and formal care staff? Specific attenti

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18

Yang, Yoo Sung. "Pastoral care for the dying." Theological Research Exchange Network (TREN), 1987. http://www.tren.com.

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19

Agapitos, Marie. "Assessing Caregivers' Hopes and Expectations for Respite Care." Thesis, Université d'Ottawa / University of Ottawa, 2016. http://hdl.handle.net/10393/34558.

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Background. While the provision of respite care is a well-known strategy for supporting caregivers of persons with dementia (PWD), it is still unclear what influences its use by caregivers. Objective. To explore respite care use through the lens of a hopes and expectations framework. Methods. Six caregivers of PWD took part in one semi-structured interview. A phenomenological approach to data collection and analysis was employed. Results. The data showed that caregivers still felt burdened despite utilizing respite care. Hopes and expectations for the PWD tended to converge for all caregivers

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20

Nasrullah, Ghany. "Caregivers’ experiences of unmet needs during palliative care." Thesis, Hälsohögskolan, Högskolan i Jönköping, HHJ, Avd. för omvårdnad, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-38616.

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Caregivers while, the biggest providers of palliative care for terminally sick patients, are often neglected in the process of providing care, which inadvertently affects their overall health and well-being. This study aims to explore the experiences of the unmet needs of the caregivers in palliative care. The literature review is based on seven quantitative, four qualitative and one mixed methodology approach studies. Results show a shortage of information given to caregivers regarding disease progression, symptomatology, support services and financial services. Furthermore the themes of unme

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21

Gunnarsson, Nina. "Discovery and management of child allergy from the parent perspective /." Stockholm : Karolinska institutet, 2007. http://diss.kib.ki.se/2007/978-91-7357-189-0/.

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22

Landon, Kelly S. "Caregivers take care!, a literary anthology of a journey toward shared care." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/MQ57669.pdf.

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23

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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24

Dixon, Brad J. "Training church members in hospital visitation skills." Theological Research Exchange Network (TREN), 1992. http://www.tren.com.

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25

Ladderbush, Joan Dolores. "Dementia caregivers: Educational intervention and coping styles." CSUSB ScholarWorks, 1994. https://scholarworks.lib.csusb.edu/etd-project/893.

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Caregivers of dementia patients who were referred to a community-based comprehensive assessment program for demented and/or chronically ill older adults by physicians or community agencies were studied for this thesis.

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26

Woodward, James Welford. "A study of the role of the acute health care chaplain in England." n.p, 1998. http://ethos.bl.uk/.

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27

Battle, Rachael Florita. "Family Caregivers' Perspectives on Establishing Hospice Care in Belize." ScholarWorks, 2019. https://scholarworks.waldenu.edu/dissertations/6970.

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End-of-life (EOL) care decisions present a challenge for family caregivers. Despite the increasing number of terminally ill patients in need of pain management and comfort care, there is limited qualitative data about how populations in the developing world can access culturally appropriate resources and EOL support. In this phenomenological study, 17 Garifuna family caregivers in southern Belize were interviewed about their experience caring for terminally family members. The conceptual frameworks were Kübler-Ross’s hospice approach and Watson’s theory of human caring. The two theories were s

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28

Rosenberg, Russell Paul. "The role of attributional style and family routine in mediating stress-illness relationships in children and their primary caregivers /." The Ohio State University, 1987. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487329662146255.

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29

Washington, Karla Thomasson Parker-Oliver Debra. "Psychosocial influences on total pain management by informal hospice caregivers." Diss., Columbia, Mo. : University of Missouri--Columbia, 2009. http://hdl.handle.net/10355/6764.

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Title from PDF of title page (University of Missouri--Columbia, viewed on March 30, 2010). The entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file. Dissertation advisor: Dr. Debra Parker Oliver. Vita. Includes bibliographical references.

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30

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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31

Snow-Spracklin, Elizabeth G. "Caregivers' perception of health, burden, social support, and care receiver problems." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape17/PQDD_0014/MQ36179.pdf.

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32

Stanley, Vicki J. "Decision-Making Processes of Primary Informal Caregivers Regarding Care Recipients' Moves to Memory Care." Digital Archive @ GSU, 2011. http://digitalarchive.gsu.edu/gerontology_theses/25.

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Most persons with a dementia are cared for in the home by family members who experience a broad and considerable amount of stress and whose caregiving careers may include planning for or initiating moves to memory care units (MCUs). This study examines the decision-making processes of primary informal caregivers regarding their care recipients' moves to MCUs. Grounded theory methods were used to collect and analyze data in two long-term care (LTC) facilities varying in characteristics including capacity, state licensure, fees, and resident profiles. Specific aims are two-fold: 1) advance an un

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33

Swann, Shanonn Pauline Pohatu. "The imagination of care : caregivers’ perspectives on end of life care in rest homes." Thesis, University of Canterbury. Sociology, 2015. http://hdl.handle.net/10092/10236.

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This study explores and examines the roles of caregivers within rest home facilities in New Zealand; and specifically, how they unpack and deal with managing the tensions associated with end of life (EOL) care. It adopted a qualitative perspective to enable an exploration of how the experiences of caregivers help guide their practice and understanding of their roles in relation to EOL care. A grounded theory framework was utilised in order to explore how caregivers make meaning and find value in the roles they perform within rest home facilities. This study offers insights into some of the ten

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34

Ponthier, Nathalie. "Les réseaux de santé : espaces de cooperation entre professionnels et patients : étude comparative de deux reseaux de sante diabète." Thesis, Lyon 2, 2012. http://www.theses.fr/2012LYO20013/document.

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La loi du 4 mars 2002 relative aux droits des malades et à la qualité du système de soins donne une définition unique des réseaux de santé. Ils représentent aujourd’hui une forme organisationnelle inscrite dans les politiques régionales de santé et sont soutenus financièrement par les agences régionales de santé (ARS). La recherche menée a pour objet la participation des personnes malades au fonctionnement et à l’activité d’un réseau de santé. En effet, si les textes législatifs consacrent la place de l’usager dans le système de soins et si la politique de santé proclame sa participation, qu’e

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35

Palacios, Josefa. "Elderly care in Chile : policies for and experiences of family caregivers." Thesis, Rennes 1, 2017. http://www.theses.fr/2017REN1G010/document.

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Dans le contexte de vieillissement de la population, un déclin potentiel du nombre des aidants familiaux et le déficit de care qui en résulte, la prise en charge des personnes âgées est restée un sujet presque invisible pour les politiques publiques et la recherche au Chili. Le gouvernement chilien a commencé à prêter attention au sujet, mais beaucoup reste à faire pour une bonne prise en charge. Cette thèse adopte le point de vue des aidant-e-s qui consacrent leur vie à aider un parent âgé en perte d’autonomie. Le care est abordée dans une perspective microsociologique en explorant la vie quo

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36

Stein, Donald M. "Pastoral care groups." Online full text .pdf document, available to Fuller patrons only, 2001. http://www.tren.com.

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37

Polasky, Samantha N. "Perceptions of Health Care for Children from Caregivers in Perceived Poverty." University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1459887381.

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38

Potter, Andrew Joseph. "Informal caregivers and the health of older adult care-recipients." Diss., University of Iowa, 2016. https://ir.uiowa.edu/etd/2260.

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Family and friends provide substantial daily assistance to older adults with disabilities, but little is known about how that caregiving impacts the health of older adults. Using survey data on a nationally-representative sample of older adults and their caregivers, matched with Medicare claims, I explored several aspects of the relationship between caregiving and the health of older adults receiving care. I relied largely on Andersen’s behavioral model, which describes health services use as a product of predisposing, enabling, and need characteristics. I found that 33%-37% of older adults wi

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39

Howard, Arianna. "ILLUMINATING PRACTICES OF EDUCATIONAL CARE AMONG FEMALE AFRICAN AMERICAN CAREGIVERS." The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1480516735305684.

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40

Hardin, Annelise Cecile. "Oral Health Knowledge of Caregivers in a Primary Care Setting." VCU Scholars Compass, 2006. http://scholarscompass.vcu.edu/etd_retro/71.

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Purpose: The purpose of this study is to assess the impact of preventive dental services (screening, oral health education, and fluoride varnish) given by pediatric medical providers with an assessment of caregivers interviewed at baseline and at 6-months follow-up.Methods: Using a prospective cohort study design, an oral health knowledge and socio-demographic questionnaire was delivered to a cross-section of caregivers of preschool-aged children seen at VCU Children's Pavilion. Baseline data was used to conduct a cross-sectional analysis of caregivers prior to their children receiving prevent

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41

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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42

Bigatti, Silvia Marcela. "Relationships between perceived burden, physical health, and health care use among spouses of people with fibromyalgia syndrome /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 2000. http://wwwlib.umi.com/cr/ucsd/fullcit?p9970686.

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43

Shlosberg, Emma. "Dementia : the burden of care on the carers." Thesis, Bangor University, 1998. https://research.bangor.ac.uk/portal/en/theses/dementia--the-burden-of-care-on-the-carers(3829ec44-fee0-4540-b783-6c78a327c567).html.

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44

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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45

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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46

O'Sullivan, Amy K. "Caregivers to the elderly with dementia informal care provided, employment choices, and formal care arranged /." Available to US Hopkins community, 2002. http://wwwlib.umi.com/dissertations/dlnow/3068193.

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47

Nilsson, Annika. "Musculoskeletal Pain among Health Care Staff : Riskfactors for Pain, Disability and Sick leave." Doctoral thesis, Uppsala University, Department of Public Health and Caring Sciences, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-8370.

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<p>The present thesis is based on four empirical studies concerning risk factors related to musculoskeletal pain (MSP), disability, and sick leave among three non-clinical samples of health care staff. Initially, in Study I, cognitive, behavioural and environmental factors related to MSP of nurses' aides<b> </b>were explored. An experimental design including baseline, intervention and follow-ups among 29 nurses' aides<b> </b>working in a home for the elderly was used to evaluate effects of a workplace intervention based on cognitive behaviour (CB)- and conventional, symptom reduction principle

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48

Carlsson, Lars. "Healthcare and patient factors affecting sick leave : From a primary health care perspective." Doctoral thesis, Uppsala universitet, Allmänmedicin och preventivmedicin, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-327290.

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Background: For indeterminate reasons, there have been major variations in sick leave in Sweden, and many physicians have perceived sick leave assignments as burdensome. Aim: To gain more knowledge and understanding, from a perspective of primary health care, about factors in health care and patients that affect sick leave. Thereby help patients in the best way, facilitate the work of physicians and other health professionals involved in the rehabilitation process, and use the health care resources optimally. Methods: This thesis is based on a randomised controlled trial (RCT) in a primary hea

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49

Jones, Phyllis L. (Phyllis Lee). "Caregivers' Appraisal of Alzheimer's Disease Symptoms and the Relationship to Decisions About Care." Thesis, University of North Texas, 1994. https://digital.library.unt.edu/ark:/67531/metadc278991/.

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The purpose of the present study was to compare 42 community-dwelling spouse and child Alzheimer's Disease caregivers with 38 community-dwelling potential caregivers on salience of illness symptoms, and accuracy of judging symptoms of illnesses.

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50

Jansson, Wallis. "Family-based dementia care : experiences from the perspective of spouses and adult children /." Stockholm, 2001. http://diss.kib.ki.se/2001/91-628-4740-6/.

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