Thematische Bibliographien / Palliative treatment / Dissertationen
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Dissertationen zum Thema „Palliative treatment“

Autor: Grafiati
Veröffentlicht am 4. Juni 2021
Zuletzt aktualisiert am 25. Juli 2025

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1

Greaves, Judith M. "Understanding palliative care: An ethnographic study of three Australian palliative care services." Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 2005. https://ro.ecu.edu.au/theses/1553.

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Palliative care commenced in Australia in the early 1980s. Although the value of palliative care has become more widely recognised by the public and other health care professionals, there is still a lack of understanding about what palliative care is and the depth and scope of this specialty area of health care. The research that I present in this thesis is based on examination of palliative care practice in a selection of Australian services, undertaken with the aim of enhancing understanding of Palliative Care. The significance of the research arises from the notion that members of the Austr
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2

Chandrasekhara, Seetha. "Palliative Treatment and Euthanasia for Psychiatric Illnesses." Master's thesis, Temple University Libraries, 2017. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/425660.

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Urban Bioethics<br>M.A.<br>When looking at the natural course of life, death is the natural conclusion. Majority of the time, people do not choose when and how they die. Death and dying are topics that are difficult to discuss for many individuals. However, when one decides to choose the context of their death, it raises many ethical considerations. Psychiatry, as a field, looks at the psychodynamics of death and dying for individuals. It is also poised to comment on the growing use of physician-assisted suicide and euthanasia for psychiatric disorders. Through a review of the literature, theo
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3

Bradley, Sarah Elizabeth. "Specialist palliative day care : patients' perspectives." Thesis, University of Hull, 2009. http://hydra.hull.ac.uk/resources/hull:3970.

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This portfolio has three parts. Part one is a systematic literature review entitled ‘Patients' Psychosocial Experiences of Attending Specialist Palliative Day Care: A Systematic Literature Review’. Recent reviews conclude that the benefits of attending Specialist Palliative Day Care are likely to be in the social, psychological and spiritual domains. However these areas are not easily identified, leaving researchers and practitioners unclear as to what aspects of these domains patients most need and desire. The objective of this review was to systematically evaluate literature on patient perce
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4

Fourie, Linda. "Pain control in palliative care : a South African nursing perspective." Thesis, [S.l. : s.n.], 2008. http://dk.cput.ac.za/cgi/viewcontent.cgi?article=1029&context=td_cput.

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5

Ramadge, Joanne, University of Western Sydney, College of Social and Health Sciences, and of Nursing Family and Community Health School. "Ways of knowing cancer pain in a palliative care setting." THESIS_CSHS_NFC_Ramadage_J.xml, 2001. http://handle.uws.edu.au:8081/1959.7/428.

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Very little work has been undertaken that explores pain as a part of human existence and the inherent knowledge that accompanies it. What pain means to people and how they know their own pain is the subject of this research study.The research sought to identify ways of knowing cancer pain of six participants, each receiving palliative care at the time of this study. The themes of, balancing conflict, living with threat, always there and making sense are identified and examined to provide understanding of the ways these people know their pain. A new model of pain assessment is offered that inco
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6

Mitchell, Geoffrey Keith. "The effect of case conferences between general practitioners and palliative care specialist teams on the quality of life of dying people /." [St. Lucia, Qld.], 2004. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe18557.pdf.

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7

Bergquist, Adam. "Evaluation of the pathways palliative care program at the Denver hospice." [Denver, Colo.] : Regis University, 2008. http://165.236.235.140/lib/ABergquist2008.pdf.

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8

Uwimana, Jeannine. "Met and unmet palliative care needs for people living with HIV/AIDS in selected areas in Rwanda." Thesis, University of the Western Cape, 2005. http://etd.uwc.ac.za/index.php?module=etd&amp.

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The aim of this study was to investigate met and unmet palliative care needs for people living with HIV/AIDS in selected areas in Rwanda. The achieve this aim, the study, firstly, identified the palliative care needs of people living with HIV/AIDS, secondly, it identified the health care services available to meet these needs, and thirdly, it determined the extent to which palliative care needs were met.
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9

Liu, Chang-Han. "Effectiveness of palliative measures in treatment of dysphagia of cancer of the oesophagus." Master's thesis, University of Cape Town, 2005. http://hdl.handle.net/11427/11191.

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Includes bibliographical references (leaves 34-35).<br>Cancer of the oesophagus,one of the most common cancers amongst the black population in South Africa with "cure" in this condition often considered as a "fortunate accident" by many experts in the field of oncology due to its late presentation and common occurrence of metastasis at presentation. The palliative care team focused their attention on measures to solve the cardinal symptom of this disease, which in most cases was dysphagia. This was also the main determinant of quality of life for these patients. Therefore, the primary objectiv
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10

Painter, Mark Llewellyn. "Outcome after palliative cardiac surgery in a developing country." Master's thesis, University of Cape Town, 1990. http://hdl.handle.net/11427/25963.

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The outcome of 121 children who underwent palliative cardiac surgery at the Red Cross War Memorial Children's Hospital over a 5 year period, 1980 1984, was retrospectively examined. 79 children had systemic artery to pulmonary artery shunt operations (SPS), 40 had pulmonary artery bands (PAB) and 2 had surgical septectomies. SPS was most often done for children with Tetralogy of Fallot (TOF, 26 cases) or complex univentricular hearts with right ventricular outflow tract obstruction (27 cases). PAB was done chiefly for ventricular septa! defects, alone (VSD, 8 cases) or with coarctation of the
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11

Davison, Graydon, University of Western Sydney, College of Law and Business, and School of Management. "Innovative practice in the process of patient management in palliative care." THESIS_CLAB_MAN_Davison_G.xml, 2005. http://handle.uws.edu.au:8081/1959.7/498.

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This thesis examines the management of multidisciplinary teams in a highly innovative environment through a study of multidisciplinary patient care teams in palliative care. It investigates management that enables spontaneous innovation where necessary, yet maintains discipline and compliance with legislation, regulation and policy. To assist the explanation a model of palliative care multidisciplinary team management and operation is developed, building on work described in the continuous innovation and organisational configuration literatures. This thesis describes innovative practices as fo
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12

Garanganga, Eunice. "Palliative care needs of children suffering from AIDS, Zimbabwe." Thesis, [S.l. : s.n.], 2009. http://dk.cput.ac.za/cgi/viewcontent.cgi?article=1030&context=td_cput.

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13

Dawson, Patricia Shelagh Jean. "An exploration of bereavement intervention in palliative/hospice care programming." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/28712.

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Bereavement intervention is subsumed within palliative programme philosophy which encompasses the family as the unit of care and provides a continuum of care that extends beyond the death of a family member. There is no available research on the effect of post-bereavement intervention within palliative programming, and very limited research exists that evaluates the effect of intervention on bereavement outcome. This exploratory study endeavors to differentiate bereavement outcome between two populations having palliative/hospice program support but only one choosing to participate in bereavem
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Law, Chi-ching. "Can integrated palliative care services enhance the quality of end-of-life cancer care?" Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B42994949.

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15

Davison, Graydon. "Innovative practice in the process of patient management in palliative care." Thesis, View Thesis, 2005. http://handle.uws.edu.au:8081/1959.7/498.

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This thesis examines the management of multidisciplinary teams in a highly innovative environment through a study of multidisciplinary patient care teams in palliative care. It investigates management that enables spontaneous innovation where necessary, yet maintains discipline and compliance with legislation, regulation and policy. To assist the explanation a model of palliative care multidisciplinary team management and operation is developed, building on work described in the continuous innovation and organisational configuration literatures. This thesis describes innovative practices as fo
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16

Ramadge, Joanne. "Ways of knowing cancer pain in a palliative care setting." Thesis, View thesis View thesis, 2001. http://handle.uws.edu.au:8081/1959.7/428.

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Very little work has been undertaken that explores pain as a part of human existence and the inherent knowledge that accompanies it. What pain means to people and how they know their own pain is the subject of this research study.The research sought to identify ways of knowing cancer pain of six participants, each receiving palliative care at the time of this study. The themes of, balancing conflict, living with threat, always there and making sense are identified and examined to provide understanding of the ways these people know their pain. A new model of pain assessment is offered that inco
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17

Watts, Tessa Elisabeth. "Educating undergraduate pre-registration nursing students for complexity in contemporary palliative nursing." Thesis, Swansea University, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.678375.

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18

Ali, Murtaza Najabat. "Development of auxetic polymeric stent-graft for the palliative treatment of oesophageal cancer." Thesis, University of Sheffield, 2012. http://etheses.whiterose.ac.uk/2862/.

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Oesophageal cancer is the ninth leading cause of malignant cancer death and its prognosis remains poor, ranking as the sixth frequent cause of death in the world. This research work is aimed to use Auxetic (rotating-squares) geometry, only theoretically predicted and analysed by (Grima and Evans 2000), for the production of a novel Auxetic oesophageal stents and stent-grafts relevant to the palliative treatment of oesophageal cancer and also for the prevention of dysphagia. This study also endeavoured to manufacture a significantly small diameter Auxetic oesophageal stent and stent-graft. In o
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19

Chauhan, Jyoti. "The experiences of primary caregivers providing palliative care to women living with advanced breast cancer." Thesis, University of the Western Cape, 2006. http://etd.uwc.ac.za/index.php?module=etd&action=viewtitle&id=gen8Srv25Nme4_3534_1194347235.

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<p>The aim of this explorative study was to understand the experiences and challenges of primary caregivers providing palliative care to women with advanced breast cancer. This study was conducted within a qualitative research design framework underpinned by phenomenology. The significance of this study was to contribute to the knowledge that would help care professionals understand the experiences and challenges that primary caregivers face whilst providing palliative care to women with advanced breast cancer.</p>
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20

Munene, Grace N. "An Assessment of a Hospice and Palliative Care Partnership Program." Thesis, University of North Texas, 2014. https://digital.library.unt.edu/ark:/67531/metadc699969/.

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This project attempts to describe how a hospice and palliative care partnership program works. Through the assessment of one such program, the researcher sought to find out the essential components of the partnership including how the two partner organizations interact and work together. Data was collected using various methods: document review of organization documents such as newsletters, annual or quarterly reports, brochures and other available literature e.g. materials on organizations’ website and on social media; in-depth interviews with stakeholders of both organizations that included
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21

Milone, Mary Anne. "The Level of Hope in Patients Receiving Treatment for the Diagnosis of Lung Cancer." Scholarly Repository, 2010. http://scholarlyrepository.miami.edu/oa_dissertations/409.

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Lung cancer is the most common cause of cancer deaths worldwide. Hope is considered essential to life and has been positively associated with coping. The purpose of this study was to describe the level of hope in patients receiving medical treatment for lung cancer. The study was guided by Dufault and Martocchio's multidimensional theoretical model of hope. A total of 167 patients were recruited for this cross sectional descriptive study from oncology clinics in the Southeast United States. Each participant completed a nine-item demographic self-survey questionnaire and a twelve-item, four poi
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22

何孝恩 and Hau-yan Andy Ho. "Living and dying with dignity : an interpretive-systemic framework in Hong Kong." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hdl.handle.net/10722/193427.

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Protecting and promoting patients’ and families’ sense of dignity at end-of-life is an indispensable goal, one that palliative care professionals have pursued unceasingly in the modern era. While researchers have made several attempts to uncover the intricate meaning and constitution of dignity and dignified end-of-life care in recent years, their works are solely based upon a Western individualistic paradigm that may not be applicable in Eastern collective societies. This limitation underscores that the existing body of knowledge is missing an important articulation on the Chinese experience.
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23

Dignan, Debra L. "Palliative care patients and their quality of life as perceived by the patient and their caregiver." [Denver, Colo.] : Regis University, 2008. http://165.236.235.140/lib/DDignan2008.pdf.

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24

Mondejar, Pont Meritxell. "An Integrated Palliative Care System in Osona." Doctoral thesis, Universitat de Vic - Universitat Central de Catalunya, 2020. http://hdl.handle.net/10803/670065.

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L’envellida població del segle XXI pateix malalties cròniques, malalties terminals i multimorbiditat. Les cures pal·liatives han estat tradicionalment la resposta a aquestes afeccions i han evolucionat al que anomenem cures pal·liatives integrades. L’objectiu d’aquest estudi és descriure el sistema de cures pal·liatives d’Osona i identificar els elements que inclou i els que li falten com a sistema integrat en relació als elements essencials descrits a la bibliografia. Aquesta investigació ha seguit una metodologia qualitativa amb una tècnica d’estudis de cas. En conclusió els principals el
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25

Miti, Elvis Joseph. "An evaluation of a psychosocial intervention for orphans on HIV treatment: A phase II RCT of memory work therapy at PASADA, Tanzania." Master's thesis, University of Cape Town, 2015. http://hdl.handle.net/11427/16603.

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Includes bibliographical references<br>Aim: Evidence shows high burden of psychosocial problems among orphaned children with HIV. Intervention studies have generally been conducted in developed countries. This mixed methods study aimed to determine whether Memory Work (MWT) Therapy 1 week group intervention improves outcomes for this complex population, in terms of their self-esteem, coping and psychological wellbeing compared to standard care, and to establish mechanisms of action. Method/Issue: An RCT Phase II of 48 Adolescents aged 14-18, full-orphaned AIDS on ART in Tanzania, with a waitli
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Chapman, Ysanne. "Dimensions of sadness - expanding awareness of community nurses' practice in palliative care /." Title page, contents and abstract only, 1999. http://web4.library.adelaide.edu.au/theses/09PH/09phc4663.pdf.

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27

Davison, Graydon. "Innovative practice in the process of patient management in palliative care." View Thesis, 2005. http://library.uws.edu.au/adt-NUWS/public/adt-NUWS20051025.104715/index.html.

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28

Dobies, Pamela A. Roffol Herman Robert D. "Organizational design issues of establishing palliative care services in an acute care hospital." Diss., UMK access, 2005.

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Thesis (Ph. D.)--Henry W. Bloch School of Business and Public Administration and Dept. of Sociology. University of Missouri--Kansas City, 2005.<br>"A dissertation in public affairs and administration and sociology." Advisor: Robert D. Herman. Typescript. Vita. Title from "catalog record" of the print edition Description based on contents viewed June 23, 2006. Includes bibliographical references (leaves 194-204 ). Online version of the print edition.
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Law, Chi-ching, and 羅志清. "Can integrated palliative care services enhance the quality of end-of-life cancer care?" Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2009. http://hub.hku.hk/bib/B42994949.

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30

Byström, Per. "Colorectal cancer treatment and early response evaluation how do we best evaluate treatment response? /." Stockholm, 2010. http://diss.kib.ki.se/2010/978-91-7409-766-5/.

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31

Held, Mareike [Verfasser], and Olivier [Akademischer Betreuer] Morin. "A new on-board imaging treatment technique for palliative and emergency treatments in radiation oncology / Mareike Held. Betreuer: Olivier Morin." Hamburg : Staats- und Universitätsbibliothek Hamburg, 2016. http://d-nb.info/1095766643/34.

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32

Held, Mareike Verfasser], and Olivier [Akademischer Betreuer] [Morin. "A new on-board imaging treatment technique for palliative and emergency treatments in radiation oncology / Mareike Held. Betreuer: Olivier Morin." Hamburg : Staats- und Universitätsbibliothek Hamburg, 2016. http://nbn-resolving.de/urn:nbn:de:gbv:18-78319.

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33

Akhiwu, Patrick. "Home Based Care (HBC) providers knowledge attitude and perception of identification treatment and referrals of common symptoms of Acquired Immune Deficiency Syndrome (AIDS) in Botswana." Master's thesis, University of Cape Town, 2016. http://hdl.handle.net/11427/20352.

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Home based care is a major intervention in the management of HIV/AIDS and other illnesses in need of palliative care, especially in situations where resources are limited. The challenges associated with HIV/AIDS infection in Botswana resulted in the training of home based care volunteers (HBCV) to assist in the fight against HIV/AIDS. The HBCV regularly visit and assist ill patients at home. They provided support with home activities and basic health care. They are to note changes in their clients' condition, and, if necessary, report to the home based team at the clinics f or further action.
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34

McConigley, Ruth. "Rural palliative care nursing: A modified grounded theory study." Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 1998. https://ro.ecu.edu.au/theses/986.

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This paper presents the findings of a study of rural palliative care nurses in Western Australia. The numbers of rural centres in Western Australia offering palliative care services are increasing; however at present there is little empirical data available about the roles of the nurses involved. This study was undertaken to begin to correct this deficit. The study examines basic social processes associated with the role of rural palliative care nurses and identities issues that affect the nurses’ professional practice. A modified grounded theory approach was used to form a conceptual framewor
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35

MacLeod, Roderick D. "Changing the way that doctors learn to care for people who are dying." Thesis, University of South Wales, 2001. https://pure.southwales.ac.uk/en/studentthesis/changing-the-way-that-doctors-learn-to-care-for-people-who-are-dying(a13ed38e-49a2-42de-a112-180e68e4339d).html.

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This collection of work represents an interest in education in palliative care over the last ten years. These papers are written either by myself or in collaboration with colleagues in Britain and New Zealand. During those years the way in which palliative care is taught and learned has changed and continues to change. The overview of the work submitted here describes the rationale behind the development of new approaches to the teaching and learning of care at the end of life. In many ways this collection represents a personal journey - one that involves investigation, growth, research and ev
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36

Hill, Hazel Catherine. "Psychosocial support within the everyday work of hospice ward nurses : an observational study." Thesis, University of Stirling, 2016. http://hdl.handle.net/1893/24356.

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Psychosocial support is said to be an inherent component of nursing care and a major focus of palliative care. Literature exists which outlines perceptions of the psychosocial needs of patients and how psychosocial support should be provided. However, there is a lack of empirical evidence on how psychosocial support is operationalised in practice. This study provides a valuable and substantial new contribution to the evidence on the psychosocial needs expressed by patients in a hospice ward and how nurses immediately respond to these needs within their everyday practice. A study gathering data
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Farrant, Lindsay Georgina. "A survey of the prevalence and burden of pain and symptoms amongst HIV positive patients attending HIV treatment clinics in the University of the Witwatersrand Academic Hospital clinics." Master's thesis, University of Cape Town, 2011. http://hdl.handle.net/11427/10472.

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This study was designed to measure the symptom prevalence and symptom burden amongst patients attending three HIV treatment clinics in greater Johannesburg, and to assess the relationship of these to CD4 count, viral load, WHO stage, functional status and HAART. Patients at the three clinics were invited, using convenience sampling, to participate in completing the interviewer administered Memorial Symptom Assessment Scale-Short Form (MSAS-SF) which assesses the 7 day prevalence and distress for 28 physical symptoms and prevalence and frequency of four psychological symptoms. Demographic and c
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38

Cohen, Lynne. "Attitudes of nurses to palliative care in nursing homes in the Perth metropolitan region." Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 1995. https://ro.ecu.edu.au/theses/1179.

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Zanna and Rempel (1988) have proposed that attitudes are a summary evaluation of an attitude object based on three classes of information, namely: cognitive information, affective information and behavioural information. This model has mainly been tested in the social groups and social policies area investigating two classes of information: cognitive and affective, and therefore there is a need for research to test the validity of this model in other areas. The present study applies the model to the area of palliative care in nursing homes. 76 directors of nursing, 76 clinical nurse specialist
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Reid, Noreen. "An action research study to investigate the strategies that can be used by health care professionals, during video consultations with palliative care patients, to enhance the therapeutic alliance." Thesis, University of Stirling, 2017. http://hdl.handle.net/1893/27690.

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Background: The use of telemedicine was gaining momentum. Although the strength of the therapeutic alliance (TA) correlated with treatment outcomes, there was no research exploring the skills, attitudes and behaviours that enhanced the TA during Skype consultations in palliative care. Aims: This study identified the skills, attitudes and behaviours that affected the TA between palliative care patients and health care professionals during Skype consultations and identified strategies that enhanced the TA. Study Design: Two cycles of action research engaged the participants in self-reflective in
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Tanner, Carolyn A. "Perception of palliative care practice of health care professionals in a mental institution : a descriptive study." Thesis, University of British Columbia, 1991. http://hdl.handle.net/2429/29703.

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The purpose of this descriptive study is to investigate the perception of practice of health care professionals at a mental institution, as it pertains to their work with dying patients, and also to identify areas of change. The conceptual framework is constructed of six factors important to palliative care that have been identified from the literature. These are personal death anxiety, organizational structure of the hospital system, role expectations of professionals, teamwork, education and training for care of the dying, and conveyance and exchange of diagnostic information. The sample sur
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Ferrel, Cynthia Lynn. "The experience of critical care nurses in initiating hospice care." abstract and full text PDF (free order & download UNR users only), 2008. http://0-gateway.proquest.com.innopac.library.unr.edu/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:1453534.

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42

Velupillai, Yoganathan. "A comparison of palliative care needs and palliative care services for community based patients with cancer and non-cancer illnesses in the Greater Glasgow NHS Board area." Thesis, Connect to e-thesis, 2004. http://theses.gla.ac.uk/1022/.

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Thesis (Ph.D.) - University of Glasgow, 2004.<br>Ph.D thesis submitted to the Departments of Public Health and Palliative Medicine, Faculty of Medicine, University of Glasgow, 2004. Includes bibliographical references (p. 272-293). Print version also available. Mode of access : World Wide Web. System requirements : Adobe Acrobat reader required to view PDF document.
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Phillips, Jane Louise. "Navigating a palliative approach in residential aged care using a population based focus." View thesis, 2008. http://handle.uws.edu.au:8081/1959.7/33324.

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Thesis (Ph.D.)--University of Western Sydney, 2008.<br>A thesis submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy to the College of Health and Science, School of Nursing, University of Western Sydney. Includes bibliography.
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44

Carolan, Clare. "The experience of emotional distress and help-seeking for distress in families living with advanced cancer and receiving palliative care : a multi-perspective case study approach." Thesis, University of Stirling, 2018. http://hdl.handle.net/1893/28047.

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The emotional impact of serious illness in families is recognised. To enhance well-being in families living we must understand how distress is experienced within families; from this, evidenced-based systemic distress interventions can be derived. However, the success of systemic intervention programmes is reliant on whether families will seek help (or not) for distress. This PhD by publication explores emotional distress and help-seeking in families living with advanced cancer. Papers one and two used systematic review techniques. Paper one evidenced distress as a systemic construct and propos
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Grove, Jan. "An evaluation of the current practices followed by oncologists in private practice in Cape Town, South Africa, in the management of patients with advanced cancer which no longer responds to anticancer treatment and the identification of the needs associated with such management." Master's thesis, University of Cape Town, 2014. http://hdl.handle.net/11427/12646.

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Includes abstract.~Includes bibliographical references.<br>Managing patients whose disease has become unresponsive to anticancer treatment confronts oncologists with major stressors which may range from the management of distressing physical symptoms to complex psychosocial issues. These sets of circumstances prompted the undertaking of this study: An evaluation of the current practices followed by oncologists in private practice in Cape Town, South Africa, in the management of patients with advanced cancer which no longer responds to anticancer treatment and the identification of the needs as
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Day, Michele Oliver Debra. "Team communication and collaboration in hospice pain management." Diss., Columbia, Mo. : University of Missouri--Columbia, 2008. http://hdl.handle.net/10355/6632.

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Title from PDF of title page (University of Missouri--Columbia, viewed on Feb 25, 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 Oliver. Vita. Includes bibliographical references.
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Magnusson, Carlsson Therése, and Elin Larsson. "Smärta och dess olika samband i livets slutskede." Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-270536.

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Bakgrund: Palliativ vård syftar bland annat till att lindra lidande och symtom som smärta och ångest. För att kunna bedöma, utvärdera samt lindra symtomen behövs smärtskattningsinstument användas. Att lindra dessa symtom främjar livskvaliteten hos patienter i en palliativ fas. Genom det Svenska palliativregistret finns möjlighet att sammanställa och utvärdera information som kan främja forskning och därmed bidra till ett minskat lidande. Syfte: Syftet är att undersöka förekomst av smärta och smärtlindring i livets slutskede samt se i vilken utsträckning validerade instrument används. Syftet är
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Jumah, Anne Mukeli. "The nature and extent of palliative care in the Nairobi Hospice." Diss., Pretoria : [s.n.], 2008. http://upetd.up.ac.za/thesis/available/etd-11202008-163831.

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Gentry, W. Michael. "A comparison of two palliative methods of intervention for the treatment of mathematics anxiety among female college students." Diss., Virginia Polytechnic Institute and State University, 1986. http://hdl.handle.net/10919/53620.

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Bandura’s (1978) self-efficacy theory provided the conceptual basis for two math-anxiety interventions: cognitive restructuring (CR) and modified progressive relaxation (MPR). These two palliative techniques were chosen since considerable evidence exists which indicates that both intrapsychic and symptom-directed methods are effective as therapeutic interventions for a wide range of stress-related problems. In addition to the treatment variable, there were two other independent variables: level of achievement in mathematics (SAT), and level of participation in mathematics (remedial, intermedia
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Fan, HaiYan (LingLing), and University of Lethbridge Faculty of Arts and Science. "Medical encounters in "closed religious communities" : palliative care for Low German-Speaking Mennonite people." Thesis, Lethbridge, Alta. : University of Lethbridge, Dept. of Anthropology and Health Sciences, 2011, 2011. http://hdl.handle.net/10133/3079.

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This multi-sited ethnography focuses on beliefs and practices associated with death, dying, and palliative care among the Low German-Speaking (LGS) Mennonites. The qualitative data, collected through participant-observation fieldwork and interviews conducted in three LGS Mennonite communities in Mexico and Canada, show a gap between official definitions of palliative care and its practice in real life. The LGS Mennonites’ care for their dying members, in reality, is integrated into their community lives that emphasize or reinforce discipleship by promoting the practices of mutual aid, social n
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