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Tesis sobre el tema "Chronically ill"

Autor: Grafiati

Publicado: 4 de junio de 2021

Última modificación: 25 de julio de 2025

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1

Coppa, Kay. "Self-help groups in the Hunter region : a qualitative study of their role in chronic illness management /." [St. Lucia, Qld. : s.n.], 2002. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe16644.pdf.

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2

Stanberry-Beall, Jenny Kay. "Building a case for lifespan respite the effects of formal respite care on caregivers of family members with chronic dependencies /." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 242 p, 2007. http://proquest.umi.com/pqdweb?did=1251902551&sid=1&Fmt=2&clientId=8331&RQT=309&VName=PQD.

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3

Fiala, Samuel E. "Camp counselors working with chronically ill children." Texas A&M University, 2005. http://hdl.handle.net/1969.1/3210.

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A growing body of empirical evidence suggests that attending specialized summer camps is beneficial for chronically ill youth (Briery & Rabian, 1999). However, there is some inconsistency across studies regarding these benefits (Hazzard & Angert, 1986). One potential explanation for these differences across camps is that they may differ in how well they recruit and train effective volunteer camp counselors. This possibility cannot be explored until more research is conducted identifying what type of person volunteers to work with chronically ill children and how they differ from others. In res

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4

Lindström, Caisa. "Burnout in parents of chronically ill children." Doctoral thesis, Örebro universitet, Institutionen för hälsovetenskaper, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-47391.

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Parents of children with a chronic disease are usually highly involved in their child’s treatment and may be affected by the heavy demands and constant stress. This can increase the risk of developing burnout, which is an individual reaction to long-term stress consisting of symptoms associated with emotional exhaustion, as well as physical and cognitive fatigue. The overall aim was to estimate the prevalence of burnout in parents of children with Type 1 Diabetes Mellitus (T1DM) and inflammatory bowel disease (IBD) (paper I), identify the risk factors associated with parenting a child with T1D

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5

Elzen, Henrike Anje. "Self-management for chronically ill older people." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 2006. http://irs.ub.rug.nl/ppn/297661620.

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6

Lees, Nancy Berman. "The self-esteem of chronically ill adolescents." CSUSB ScholarWorks, 1991. https://scholarworks.lib.csusb.edu/etd-project/852.

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7

Fung, Shuk-man Amy. "Psychosocial risk and protective factors in chronic childhood illnesses : the case of thalassaemia major /." Hong Kong : University of Hong Kong, 1996. http://sunzi.lib.hku.hk/hkuto/record.jsp?B17390084.

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8

Steuten, Lotte Maria Gertruda. "Evaluation of disease management programmes for chronically ill." Maastricht : Maastricht : UPM, Universitaire Pers Maastricht ; University Library, Maastricht University [Host], 2006. http://arno.unimaas.nl/show.cgi?fid=7668.

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9

Turner, Roxanne. "Depression in older persons who are chronically ill." DigitalCommons@Robert W. Woodruff Library, Atlanta University Center, 1990. http://digitalcommons.auctr.edu/dissertations/1471.

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This study explores the severity of depression in older persons who are chronically ill. The study was an attempt to determine if there is a significant relationship between four independent variables—family support, social support, marital status, and gender. The study was conducted while respondents were hospitalized at Clayton General Hospital. The research concluded that most older chronically ill persons were not depressed or were only mildly depressed. Significant factors were gender. Females reported more incidence of depression than males and single respondents reported higher incidenc

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10

Driskill, Gail. "Chronically Ill Children: Maternal Stress and Psychological Symptomatology." Thesis, University of North Texas, 1995. https://digital.library.unt.edu/ark:/67531/metadc279114/.

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This study used a parenting stress and coping model to identify predictors of symptomatology for 13 8 mothers of medically compromised children. This model proposed that: child characteristics (severity of the chronic illness and child related parenting stressors); parent characteristics (self-esteem, sense of competence, and parents' perceived stress/distress); and environmental characteristics (social support, general life stressor events, and demographic variables) contribute to psychological symptomatology for these mothers. Multiple regression analysis found a relationship between general

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11

Salmond, Susan Warner. "Perceptions of health care needs of the chronically ill population according to stage of illness /." Access Digital Full Text version, 1987. http://pocketknowledge.tc.columbia.edu/home.php/bybib/10692733.

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12

Routt, Katherine M. "The process of families creating meaning of chronic illness and the medical community." Online version, 2000. http://www.uwstout.edu/lib/thesis/2000/2000routtk.pdf.

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13

Lemons, Paul M. "Development of a pulmonary rehabilitation program : a biopsychosocial approach /." Master's thesis, This resource online, 1990. http://scholar.lib.vt.edu/theses/available/etd-01202010-020100/.

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14

Rodak, Rina S. "Chronically and terminally ill children and medical decision-making." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/MQ55708.pdf.

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15

Newman, Andrea Ardele. "The healing nature of dwelling." Thesis, Montana State University, 2008. http://etd.lib.montana.edu/etd/2008/newman/NewmanA0508.pdf.

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My thesis will discuss the historical pattern of mistreatment and misunderstanding of the chronically mentally ill and the continued struggle the population faces. I believe that architecture holds some of the answers for these issues concerning the "ill" and that environmental factors do play a large part in the effective treatment of this population. It is my intention to design a facility where the chronically mentally ill can live and communicate freely without the stigma that has plagued them for so long. I will use the tools that social theory, philosophers such as Heidegger and the conc

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16

Thompson, Jacquelyn J. "How chronic illness affects family relationships and the individual." Online version, 2009. http://www.uwstout.edu/lib/thesis/2009/2009thompsonj.pdf.

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17

Reich, Julie A. "Perceptions of Parental Differential Treatment: Correlates in Chronically Ill and Non-Ill Samples of Children." [Tampa, Fla.] : University of South Florida, 2003. http://purl.fcla.edu/fcla/etd/SFE0000063.

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18

Hagen, Brad Francis. "Evaluation of education and support initiatives for family caregivers." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape17/PQDD_0025/NQ34265.pdf.

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19

Tsui, Jin-ching Wilson. "Control, appraisals, and coping as predictors of health outcomes in chinese patients with chronic illness." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1994. http://hub.hku.hk/bib/B29695624.

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20

Alcock, Denise. "Information processing analysis of chronically ill children's problem solving abilities." Thesis, University of Ottawa (Canada), 1986. http://hdl.handle.net/10393/4709.

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21

Myers, Basil Joseph. "School, hospital information exchange, boundary spanning for chronically ill children." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq20759.pdf.

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22

Pellack, David. "The chronically homeless mentally ill characteristics that predict program compliance /." [Bloomington, Ind.] : Indiana University, 2007. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3297096.

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Thesis (Ph.D.)--Indiana University, Dept. of Counseling Psychology, 2007.<br>Title from dissertation home page (viewed Sept. 25, 2008). Source: Dissertation Abstracts International, Volume: 69-02, Section: A, page: 0519. Adviser: Michael L. Tracy.

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23

West, Tousha Terrell. "An evaluation study of the homeless chronically mentally ill program." DigitalCommons@Robert W. Woodruff Library, Atlanta University Center, 1997. http://digitalcommons.auctr.edu/dissertations/573.

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This is an summative evaluation of the Homeless Chronically Mentally Ill program which examined the impact of case management and the outcome of the program on participant's substance abuse usage. Twenty-six participants' participated in the study. Participants were evaluated by two scales, the Client Satisfaction Questionnaire and the Reid-Gundlach Social Service Satisfaction Scale. Participants were sampled from those who were admitted into the HCMI program. The result of the study revealed that the majority (73.1) of those surveyed were satisfied overall with the program and 73.1 percent fe

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24

Ioannou, Chrissi. "Acute pain in chronically ill children : psychological assessment and intervention." Thesis, University of Leicester, 1992. http://hdl.handle.net/2381/34660.

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Five separate studies are reported on two groups of chronically ill children: children with end-stage renal failure who had received renal transplants and children with insulin dependent diabetes mellitus (IDDM). Assessment studies of both these groups investigated psychosocial factors influencing children's anxiety, pain and distress during venipunctures. Behavioural, cognitive and physiological measures of pain were used as well as standardized and structured interview questionnaires. The assessment studies involved 21 renal transplant children and 62 chidren with IDDM. The results found a r

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25

Fritts, Sharon Louise. "The impact of chronic illness on the family, the educators, and the community : an ethnographic research study /." For electronic version search Digital dissertations database. Restricted to UC campuses. Access is free to UC campus dissertations, 2004. http://uclibs.org/PID/11984.

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Thesis (Ph. D.)--Joint Doctoral Program in Educational Leadership (California State University, Fresno and University of California, Davis).<br>Typescript. Includes bibliographical references. Also available via the World Wide Web. (Restricted to UC campuses)

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26

Hrabe, David Paul. "Relationship development among chronically ill women in a computer-mediated environment." Diss., The University of Arizona, 2001. http://hdl.handle.net/10150/280117.

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The purpose of this study was to determine the stages and processes of relationship development in a computer-mediated support group. Using grounded theory methodology, a secondary data analysis was conducted of 22 weeks of textual message exchanges among 15 chronically ill women. The study's outcome is a new middle range theory, Connecting in Cyberspace. This theoretical framework is the first attempt to describe the processes and phases of a computer-mediated support group and is intended as a beginning guide for nursing practice in an electronic environment. Orienting is defined as the star

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27

Kleynshteyn, Inna. "Social Connectedness and the Quality of Life in Chronically Ill Patients." UNF Digital Commons, 2013. http://digitalcommons.unf.edu/etd/451.

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Social connectedness, feelings of belonging and closeness with the social world, has been identified as an important aspect for the physical, emotional, and collective well-being. People faced with chronic illness may feel like they no longer belong, and this lack of connectedness may have a negative impact on health, well-being, and psychological functioning. The present study investigated social connectedness and quality of life in 151 patients with ongoing symptoms of chronic illness. It was hypothesized that lower levels of social connectedness would be associated with poorer health-relate

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28

Tew, Kristi L. (Kristi Lee). "The Efficacy of Filial Therapy with Families with Chronically Ill Children." Thesis, University of North Texas, 1997. https://digital.library.unt.edu/ark:/67531/metadc277594/.

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This study was designed to determine the effectiveness of Filial Therapy as a method of intervention with families with chronically ill children. Filial Therapy is an intervention that focuses on strengthening and enhancing the parent-child relationship. Parents are trained to become the agents of change for their children's behaviors by utilizing basic child-centered play therapy skills in weekly play sessions. The purpose of this study was to a) determine the effectiveness in decreasing parental stress, b) determine the effectiveness in increasing parental acceptance, and c) determine the ef

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29

Blauner, Michael Lee. "Self-help groups for the chronically ill: Different structures, varying processes." Case Western Reserve University School of Graduate Studies / OhioLINK, 1991. http://rave.ohiolink.edu/etdc/view?acc_num=case1055450373.

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30

Blubaugh, Victoria G. "Self-concept in siblings of chronically ill children : Duchenne muscular dystrophy /." The Ohio State University, 1986. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487265555440494.

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31

Chang, Pi-Chen 1964. "Social support, uncertainty, and ways of coping in chronically ill adolescents." Thesis, The University of Arizona, 1991. http://hdl.handle.net/10150/558162.

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32

Cheng, Ka-ki. "Is chronic illness associated with the occurrence of intimate partner violence? /." View the Table of Contents & Abstract, 2006. http://sunzi.lib.hku.hk/hkuto/record/B36396916.

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33

Greenbergs, Helen Lea. "Sexual adjustment in couples living with systemic sclerosis /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 1997. http://wwwlib.umi.com/cr/ucsd/fullcit?p9728768.

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34

Powers, Thomas V. "The relationship among protective factors, volition, and academic resilience in chronically-ill adolescents /." Thesis, Connect to this title online; UW restricted, 2003. http://hdl.handle.net/1773/7863.

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35

Jean, Raynice Eveline. "The perceptions among African American caregivers of children with chronic illnesses /." Digital version accessible at:, 1999. http://wwwlib.umi.com/cr/utexas/main.

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36

Shiu, Shiona. "Achieving equity in educational outcomes for students with chronic illness." View thesis, 2008. http://handle.uws.edu.au:8081/1959.7/19222.

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Thesis (Ed.D.)--University of Western Sydney, 2008.<br>A thesis submitted to the University of Western Sydney, College of Arts, School of Education, in fulfilment of the requirements for the degree of Doctor of Education. Includes bibliography.

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37

McIlroy, Charles R. "Aftercare for the chronically mentally ill utilizing church resources in the community /." Theological Research Exchange Network (TREN), 1985. http://www.tren.com.

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38

Torri, Dischinger Maria Inês. "Loss of Resources and Demoralization in the Chronically Ill: A Mediation Model." UNF Digital Commons, 2016. http://digitalcommons.unf.edu/etd/649.

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In order to obtain a closer look into the psychosocial impact of chronic conditions, symptom severity, loss of resources, and demoralization were investigated through a mediation analysis. The function and implication of social support was also explored within the circumstances of chronic conditions. Lastly, symptom chronicity was probed as an influential element in the understanding of the consequences of being chronically ill. Participants were 200 men and women, with a mean age of 46 years, and the dataset came from the VOICE (Verification of Illness and Coping Experience) survey. The conce

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39

Allgood-Scott, Jill R. "A study of health care utilization among chronically ill rural older adults." free to MU campus, to others for purchase, 1998. http://wwwlib.umi.com/cr/mo/fullcit?p9901213.

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40

English, Amber L. "Measuring parenting stress in those with chronically ill children: A psychometric evaluation." Thesis, English, Amber L. (2020) Measuring parenting stress in those with chronically ill children: A psychometric evaluation. Masters by Coursework thesis, Murdoch University, 2020. https://researchrepository.murdoch.edu.au/id/eprint/60896/.

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This study examined the measurement of parenting stress in caregivers of chronically ill children (N=203). The evaluation was focussed on the two most popular measures in the literature; the Parenting Stress Index-Short Form and the Paediatric Inventory for Parents. The Parenting Stress Index-Short Form (PSI-SF) it the most commonly used measure. However, while the PSI-SF has been well-supported in the healthy populations it was designed for, the evidence was poor for its utility with parents of chronically ill children. The Paediatric Inventory for Parents (PIP), developed with parents of chi

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41

Neimeyer, Jennifer. "The Impact of a Coordinated Care Program on Uninsured, Chronically Ill Patients." VCU Scholars Compass, 2010. https://scholarscompass.vcu.edu/etd/2038.

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This study explored how being enrolled in a program that both coordinates patient care and provides a medical home changes health care utilization for uninsured patients, more specifically those persons with chronic conditions, through the use of the Chronic Care Model and Andersen and Aday’s Behavioral Model for Access to Health Care. Uninsured patients typically seek out care in a fragmented manner, which may lead to ineffective and inefficient care, especially for conditions that may require ongoing treatment and monitoring such as chronic conditions. The methodology used to examine the rel

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42

Bracey, Kimberly Vaunterice. "Experiences of Parents With Chronically Ill Children Regarding the Affordable Care Act." ScholarWorks, 2019. https://scholarworks.waldenu.edu/dissertations/6975.

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Ways in which the implementation of the Patient Protection and Affordable Care Act (ACA) affect parents with chronically ill children are not well understood. The purpose of this phenomenographic study was to gain greater insight into the perceived experiences of parents of chronically ill children regarding implementation of the ACA in a southern state. Argyris's intervention theory provided the framework for the study. Face-to-face interviews were conducted with a purposeful sample of 12 female parents who are caregivers of chronically ill children. Data were analyzed and coded to identify c

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43

Cordingly, Kimberly Lynne. "The emerging geographies of work and identity exploring alternative employment strategies and work subjectivities of women with multiple sclerosis (MS) /." Morgantown, W. Va. : [West Virginia University Libraries], 2007. https://eidr.wvu.edu/etd/documentdata.eTD?documentid=5302.

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Thesis (Ph. D.)--West Virginia University, 2007.<br>Title from document title page. Document formatted into pages; contains x, 415 p. : col. ill. Includes abstract. Includes bibliographical references (p. 324-368).

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44

Loong, Lai-ching Eve, and 龍麗貞. "Effectiveness of chronic disease self management program (CDSMP) for non-English speaking population: a narrativeliterature review." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B46940728.

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45

Thames, Robert Milton 1955. "The chronically mentally-ill served by the public fiduciary of Pima County, Arizona." Thesis, The University of Arizona, 1987. http://hdl.handle.net/10150/276536.

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This study was a survey of the chronically mentally ill cases served by the Public Fiduciary of Pima County, Arizona made to determine differences between and among these cases in numbers, finances, living arrangements, and the nature of their involvement with the Public Fiduciary according to age, sex, ethnic group, and mental disorder. Information was collected on 89 chronically mentally ill cases. Summaries and statistical analyses were made of the collected information. Schizophrenia in its various forms was found to be the dominant illness. Over half of the cases lived in unsupervised set

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46

Larivière, Nadine. "Adjustment to community residential settings among severely and chronically mentally ill older adults." Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=31253.

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Little is known about the impact of deinstitutionalization on severely and chronically mentally ill older adults. The primary purpose of this study was to describe the adjustment process of 33 adults, aged 65 years and over, with severe and chronic psychiatric disorders, who were transferred from a psychiatric hospital to community housing facilities between 1995 and 1998. Data was collected at five periods in times, twice prior to discharge and three times following relocation. Global functioning, social behaviors, functioning in activities of daily living, cognitive status, perceived quality

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47

Milner, James Allen Sr. "The intervention and assistance to the chronically mentally ill who are experiencing homelessness." DigitalCommons@Robert W. Woodruff Library, Atlanta University Center, 2006. http://digitalcommons.auctr.edu/dissertations/560.

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The writing of this dissertation was an effort to address the issue of providing assistance to those persons who have been diagnosed with a chronic mental illness and were also experiencing homelessness. The author addresses several questions surrounding this issue. Ultimately, it was the desire of this writer to develop a Safe Haven program for this population that would create a residential service center. At this writing, there is not such a program in the State of Georgia. Among the many questions surrounding this issue that this writer addressed was: What is the history behind this proble

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48

Seidmann, Susana, Dorina Stefani, Carlos O. Pano, Luisa Acrich, and Vera Bail Pupko. "Feeling of burden and social support in family caregivers of chronically ill patients." Pontificia Universidad Católica del Perú, 2013. http://repositorio.pucp.edu.pe/index/handle/123456789/100203.

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We evaluate if the social network structure, the percei ved support and the personal satisfaction acts on the caregiver's feeling of burden, coming from the caring of a child oran older parent with chronic invalidating illness. We used Mannheim's Instrument for Social Support (1986) and the Feeling of Burden Questionnaire (Zarit & Zarit, 1999) with 143 caregivers -50,3% mothers and 49,7% daughters. Taking into account the multivariate statistical tests, we can conclude that mothers have a larger relatives network than daughters, even though they don't significantly differ in the perception of

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49

Hughes, Danielle Anna. "The Other Child: Health Narratives of Adults Raised with a Chronically Ill Sibling." Antioch University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=antioch1340378917.

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50

Wiencek, Clareen. "Symptom Burden and Its Relationship to Functional Status in the Chronically Critically Ill." Case Western Reserve University School of Graduate Studies / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=case1207241196.

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