Rozprawy doktorskie na temat „Adolescent cancer experiences”
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Till, Tracy, i res cand@acu edu au. "Coping with Cancer: the Adolescent experience". Australian Catholic University. School of Nursing, 2004. http://dlibrary.acu.edu.au/digitaltheses/public/adt-acuvp70.25092005.
Pełny tekst źródłaLopez, Alana Delores. "Transition Experiences of Adolescent Survivors of Childhood Cancer: A Qualitative Investigation". Scholar Commons, 2011. http://scholarcommons.usf.edu/etd/3213.
Pełny tekst źródłaBehar, Lynn C. "Getting through it alone : a descriptive study of the experiences of single mothers with breast cancer and adolescent children /". Thesis, Connect to this title online; UW restricted, 1999. http://hdl.handle.net/1773/11156.
Pełny tekst źródłaMelander, Anna, i Susanne Roséus. "Barnets upplevelse av förälders cancersjukdom". Thesis, Malmö högskola, Fakulteten för hälsa och samhälle (HS), 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:mau:diva-25022.
Pełny tekst źródłaIn 1999 more than 45.000 adult Swedes were diagnosed with cancer. Many of those had school age children and adolescents. Children and adolescents are those who live longest with the trauma and potential loss of a parent.The purpose of this study was to achive knowledge about childrens perceptions having a parent with cancer; their thoughts about the illness, how they are affected by their parents illness and to gain insight in what healthcare professionals can do to help the children deal with the situation. Ten articles were analysed in this literature study. The result shows that children having a parent with cancer had lots of thoughts about the disease, some became introvert and wished to escape while others were acting out with anger, aggressions or crying. Children and adolescents had anxiety problems, sleeping disorders, trouble concentrating and some even had social functioning disorders. The study showed that health care units need to provide parents with advice, support and knowledge how they can support their children cope with the situation. The health care also need to provide support groups and individual counselling for children and adolescents.
Phillips-Salimi, Celeste. "Young adult cancer survivors' experiences of connectedness with their healthcare providers". Thesis, Connect to resource online, 2009. http://hdl.handle.net/1805/2067.
Pełny tekst źródłaTitle from screen (viewed on February 2, 2010). School of Nursing, Indiana University-Purdue University Indianapolis (IUPUI). Advisor(s): Joan E. Haase, Marion E. Broome, Janet S. Carpenter, Richard M. Frankel. Includes vitae. Includes bibliographical references (leaves 227-258).
Hedström, Mariann. "Distress among Adolescents with Cancer". Doctoral thesis, Uppsala universitet, Vårdvetenskap, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4832.
Pełny tekst źródłaErickson, Jeanne. "The education experiences of eight American adolescents in cancer survivorship". Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:e366e072-075d-4f9f-8a02-308c09d8728e.
Pełny tekst źródłaMcTaggart, Deborah L. "Breast cancer experience : mothers, adolescent daughters and the mother-daughter relationship". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0018/NQ56587.pdf.
Pełny tekst źródłaKavanaugh, Brian. "Examining the Experience of Peer Relationships in Adolescents with Cancer". Antioch University / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=antioch1373627069.
Pełny tekst źródłaRechner, Mona Gale. "Adolescents with cancer : their experience living with a chronic illness". Thesis, University of British Columbia, 1989. http://hdl.handle.net/2429/27341.
Pełny tekst źródłaApplied Science, Faculty of
Nursing, School of
Graduate
Höier, Sofie, i Per Rickström. "Erfarenheter av stöd hos unga som genomgår cancerbehandling". Thesis, Högskolan i Halmstad, Sektionen för hälsa och samhälle (HOS), 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-17078.
Pełny tekst źródłaTo be struck with cancer is a very profound experience in life, particularly to the young individuals who are undergoing major transitions in the development of their identity. This development works in harmony with their surroundings concurrently while they are undergoing a process of emancipation from their parents. A cancer diagnosis can mean that the maturation process is hampered by the risk of isolation in daily life from both relatives as well as close friends. The need for support can be substantial for young people since they are young but also on their way into adulthood. The purpose of this study was to illuminate the experience of support that adolescents and young adults have while undergoing treatment for cancer. Eleven research articles were analyzed according to the purpose and the result showed that young people see family, friends, group support and the nurse as important sources of support. The most important experiences that the young people pointed out were that family and friends should treat them like before they got their cancer diagnose. They also had a wish that their care should be carried out with particular regard to the specific situation they are in and also that their contact with everyday life is facilitated. The young people also pointed out the importance of a youthful atmosphere in the adult care with an environment that is adjusted for young people, which will facilitate contact with family and friends, and also comprehensive and age-appropriate information. Young people's specific situation and needs for support when receiving treatment for cancer should be made visible in education and research.
Grimaldi, Gary. "Adolescents' lived experiences during treatment of cancer and impact on social participation". Thesis, NSUWorks, 2011. https://nsuworks.nova.edu/hpd_ot_student_dissertations/9.
Pełny tekst źródłaFochtman, Dianne. "Understanding the Meaning of the Lived Experience of Adolescents in Treatment for Cancer". Diss., University of Hawaii at Manoa, 2010. http://hdl.handle.net/10125/22052.
Pełny tekst źródłaAndersson, Johanna, i Anna-Lisa Parlapiano. "Ungdomar och unga vuxnas upplevelser av att genomgå en cancerbehandling : En litteraturstudie". Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-347840.
Pełny tekst źródłaAim: The aim of this literature study was to describe adolescents and young adults experiences of going through cancer treatment and what kind of support they would have needed during treatment. Method: A literature study has been done where eleven original articles with qualitative studies from the databases Pubmed and Cinahl were used. Results: The result were divided into four main themes; experiences of physical changes, the effects on psychological health, the effects on social life and the need for support from healthcare providers and close relations. Bodily changes were something that created insecurities and lack of control over the own body. That created anger and frustration. The result from the studies also showed that social networks, emotional support and competent healthcare providers is essential for the patients. Conclusion: Adolescents and young adults lives are very affected when going through cancer treatment. Their physical and psychological health are affected by how they get received by healthcare providers. There for, it would be of advantage if healthcare providers have knowledge about the patients experiences going through cancer treatment. To be able to give the right support and information. A confidential communication and a trustworthy relation between healthcare provider and patient is crucial for a good care. Key words: Cancer, adolescents, young adults, experiences.
Brimeyer, Chasity. "The adolescent with cancer's school re-entry experience : exploration of predictors and successful outcomes". Diss., University of Iowa, 2012. https://ir.uiowa.edu/etd/3267.
Pełny tekst źródłaMarklund, Emelie, i Frida Sundbom. "Barns och tonåringars upplevelser av att leva med en förälder som drabbats av avancerad cancersjukdom : En litteraturstudie". Thesis, Umeå universitet, Institutionen för omvårdnad, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-131597.
Pełny tekst źródłaBackground: Cancer is, globally, one of the most common diseases. Half a million Swedes recive a cancer diagnosis during their lifetime. In one day, approximately 3 Swedish children experience the loss of their parent due to cancer. To help these vulnerable children the community needs to increase knowledge of the subject in order to create better conditions for the childrens future. Aim: The aim of this litterature study was to illuinate the experiences of children and adolescents living with a parent diagnosed with advanced cancer. Metodhs: A literature study with qualitative articles was selected. The articles were found in Cinahl, PubMed and PsycINfO. Eight scientific articles conformed to the aim. The result in the studies were analyzed with help of a 5-stepmodel as described by Friberg. Results: The analysis resulted in 5 categories and 13 subcategories. The categories are: emotional reactions, how children cope with the situation, the main support, changes in family- and social life and growing with the experience. Conclusion: An open communication and to be involved in the parent´s desease is important for the children. The nurse should work in a family-centred approach to provide good care for the children.
Spies, Leana. "A study to understand the experiences of adolescents and young adults living with cancer in a northern cape public health setting". Master's thesis, Faculty of Health Sciences, 2020. http://hdl.handle.net/11427/34001.
Pełny tekst źródłaPemer, Lisa A. M., i Fredrik Willehadson. "Ungdomar och unga vuxnas upplevelser av sin psykosociala situation under cancerbehandling". Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-425599.
Pełny tekst źródłaABSTRACT Background: Adolescents and young adults undergoing cancer treatment are in need of specially adapted and age appropriate care since their age group undergoes unique life-developing milestones in the transition period between childhood and adulthood that may be affected by cancer. A disrupted life development may result in long-term negative consequences that may affect adolescents and young adults even after the end of cancer treatment. Aim: This study aimed to examine adolescents and young adults’ experiences of their psychosocial situation during cancer treatment. Method: Literature review with descriptive design. The literature search used MEDLINE, CINAHL, and PsycINFO. The result was based on eleven qualitative studies and a quantitative study with qualitative processing of a free text answer published between 2014-2020. Result: Adolescents and young adults valued the maintenance of a normal life and strived to achieve this with different strategies. Independence and the feeling for one's own identity could be disturbed. Support from family, friends, cancer-stricken peers, and healthcare staff was of importance, but not always enough. Exaltation was experienced over ending the cancer treatment but also a concern for the future afterwards. Conclusion: Reported experiences of psychosocial stress during cancer treatment lead to the conclusion that knowledge of how these challenges can be met in a specially adapted and age-appropriate way is deficient. A further in-depth understanding of adolescents and young adults' psychosocial experiences during cancer treatment from further research may potentially improve healthcare's ability to offer adequate care. Keywords: Adolescents and Young Adults (AYA), Cancer Treatment, Psychosocial, Experiences.
Cheng, Mei Ling, i 鄭美玲. "The Lived Experiences of Adolescent Cancer Patients during Hospitalization". Thesis, 1997. http://ndltd.ncl.edu.tw/handle/39387046268521596163.
Pełny tekst źródła高雄醫學院
護理學研究所
85
The purpose of this study was to explore the hospitalized exeriencesof adolescent cancer patients, and, through the understanding of this, to properly help them adapt hospitalized stress caused by cancer treatment. The method of phenomenology was implemented to understand the essential lived experiences of six adolescnet cancer patients during hospitalization.In-depth interview and tape recording were carried out in all participantsand then transcribed. The transcription of participants'' descriptions wereanalyzed by using Colaizzi''s method of phenomenology. The results of data analysis revealed that, two major groups of experience, namely ''living situation'' and ''growth energy'', were induced in the in-hospital experience structure of adolescent cancer patients. Livingsituation, a central theme in terms of ''grieving loss'', was constructed byfour categories, including ''confinement of body, time, and space''; ''threatof self-concept''; ''anxiety of uncertainty''; and ''locking of emotion''. Growth energy cultivated by the in- hospital living situation was penetratedby a central theme, ''maintaining control'', including three categories, suchas ''keeping balance of life''; ''completion of developmental task''; and ''holding of life esteem''. The results of this study indicated that, though these adolescent cancerpatients were "captive" in the limited space of hospital and endured the sufferings of physical distress, they still retained the persistence and aspirations for life and still managed to sustain fragmentary living. Thus,they were able to settle on the point between desperation and hope. Besides,they not only seized the opportunity of growth and made efforts to find livingfoothold from their illness, but also learned how to devote themselves andextended the energy of life. In this process of regaining sense of controlfrom illness, they reached the goal of growth. The study results may helphealth care professionals understand this special experience and face up tothe crisis which hospitalization might cause to the adolescent cancer pat-ients, so that the crisis of loss can be reverted to the turning point of growth by adolescent cancer patients.
Yang, Hui-Chuan, i 楊惠娟. "The illness experiences of adolescent with cancer: body and self-extension". Thesis, 2017. http://ndltd.ncl.edu.tw/handle/05929088113260922148.
Pełny tekst źródłaCheng, Kai-Yun, i 鄭凱芸. "When a parent got cancer-The experiences of adolescent girls with parental responsibilities". Thesis, 2010. http://ndltd.ncl.edu.tw/handle/01478629995367007755.
Pełny tekst źródła東海大學
社會工作學系
98
The thesis is of a primary incentive to look into the subjective perceptional behavior of adolescent girls engaging in the parenting practice in the situation as their parents suffer cancer, so as to help develop practical methods for social workers as an assistance in such condition, on top of which a general conception of ‘parentification’ here in Taiwan is to be well delved. Objects of this research are 15 teenage girls from 13 to 18. Based on intensive interviews and grounded theory, the experiential patterns of adolescent girls with family responsibilities are established. As a result in the case of the patterns, some magnificent renditions are as followed: 1. Individual episodes: a. Emotional repression as coping skill, developmental tasks as daily life: It is apparent to observe the objects withhold their emotions while taking care of their parents or siblings, who take such responsibilities also as to keeping pace up to schoolwork as well as their own personal social images in accordance with relationship among peers. b. Willingness to take the family responsibilities may be due to 4 main factors: 1. reciprocation of breeding, 2. obligatory calling, 3. pre-formed sense of responsibility, 4. unevasive circumstances. c. Benign feedbacks: In general, the objects take on affirmative verdicts to be burdened as family responsibilities regardless that more or less inevitable ‘grumbling period’ may occur. 2. Domestic association: With views to dual dimensions of emotion and financial intensity respectively, adolescent girls’ involvement in family responsibilities can be categorized into the following four types: a. diverse burden, b. whole-hearted protection, c. attached fusion, d. cogent sympathy. These four groups are also evaluated by means of objects’ handling related cancer information, schoolwork and calling to bearing the family responsibilities. 3. Environmental sustain: resource and support Objects gain various supports and aids especially in terms of extended families in either of the four types. In addition, the governmental authorities offer long-term and short-term subsidies to most of the needy cases. However, the expecting feedback of bailing out their household financial problems seems yet to be reached. Summing up the research, traditional merit ‘filial piety’ is the indigenous inducement which blends within the objects’ family responsibilities and ego development, in which the researcher provides practicing procedures and principles according to distinguishing types of each case, consulting in the mean time for setting up adolescent girls’ groups for the similar problems, which hopefully facilitate the solution of the same situation in the future.
"Experiences of adolescent bone sarcoma survivors : the journey from diagnosis through remission and beyond". Thesis, 2015. http://hdl.handle.net/10210/14749.
Pełny tekst źródłaA literature survey has confirmed that the growing number of cancer survivors in general are experiencing both physical as well as psychological and social adaptation difficulties following their cancer treatment. This is no different for patients diagnosed with Osteosarcoma and Ewing sarcoma (bone sarcomas) during adolescence. At present there is no formal psychosocial intervention program available to the patients presenting with Ewing and Osteosarcomas. Because of the multicultural nature of the patients as well as the fact that many childhood and adolescent cancers do not include major surgery, as is the case with bone sarcomas, the direct applicability of generalized psychosocial intervention programs for adolescents with cancer other than bone sarcoma is doubtful ...
Poole, Adele. "The lived experiences of adolescents with cancer". Thesis, 2010. http://hdl.handle.net/11394/3481.
Pełny tekst źródłaPeople often do not want to hear, talk or read about cancer. Cancer is arguably one of the most feared illnesses and maybe rightly so for it is usually associated with pain, fear,uncertainty, anxiety, long uncomfortable treatments and death. To receive a diagnosis of cancer must be absolutely devastating especially when you are in a developmental stage where you are already battling with issues such as self-esteem, body image, independence and career choices. The current study explored the lived experiences of adolescents who have or had cancer and how this experience impacted on their lives. Six adolescent cancer patients from the cancer unit in a public hospital were interviewed. The sample was purposively drawn and the majority of the interviews were conducted at the homes of the participants. Phenomenology was used both as a theoretical framework as well as a means of analysing data. Using the descriptive phenomenological method employed by Giorgi,four essential themes emerged from the data. The themes included (1) Unexpected change of everyday life means experiencing the unfamiliar (2) Experiencing a changed body, (3) Experiencing the support of significant others and (4) Anticipating a future. The themes were explained in terms of the four existentials of Van Manen which is lived space, lived body, lived other and lived time. The study revealed that although the initial diagnosis of cancer came as a shock to the participants and their families, they were able to deal with the inevitable changes that accompanied the diagnosis mainly as a result of the support they received from family and friends. Their initial fear of death were replaced with an ardent pursue of their dreams for the future.
Chung, Wei-Ting, i 鍾維庭. "A Study of Life Experience of Adults Who Had Cancer in Adolescent Period". Thesis, 2014. http://ndltd.ncl.edu.tw/handle/64359519644853304544.
Pełny tekst źródła國立屏東教育大學
教育心理與輔導學系碩士班
102
This study aims to investigate how adolescents’ life pattern interact with their cancer experience. There are three adults participate in this study, they all had cancer when they were 12-20 years old, and off treatment now. Data collection is based on interview, and analysis by narrative analysis method. The results are as follows: 1. Adolescents’ feeling and coping strategies to the diagnosis of cancer In this study, the three adults felt confused and shocked when they heard about the diagnosis of cancer. The coping strategies they used to adapting the suffering were do something they like, keep a feeling of hopefulness, seeking for social support, turning attention to something else, and searching information about the disease. 2. How adolescents’ life experience and support network influence their cancer experience The adults’ positive characteristics and good family support、relationship with doctors can help reducing the impact of negative feelings, and keeping faith to the treatment, being more cooperative. 3. How the experience of cancer influence the values and life after treatment Three adults in this study had positive changes in values and better relationship with families. Two adults made some limits to their life pattern, career and romances, because worrying about relapse.
Lin, Miao-Ling, i 林妙怜. "Hope Experience in Drawings by Adolescents with Bone Cancer during the Treatment". Thesis, 2016. http://ndltd.ncl.edu.tw/handle/39227436674943456612.
Pełny tekst źródła國立陽明大學
臨床護理研究所
104
Background: Hope is the universal phenomenon of human life. It can enhance life experiences as well as provide meanings to everyday life. One can share their hope searching experience to encourage others in having a better outlook of their illnesses. Objective: This study utilized a phenomenological approach to explore the hopeful experiences of post-operative adolescents bone cancer patients through figure drawings. The patient's overall descriptive hopeful experience was explored using the Snyder's theoretical concept of hope. Method: Phenomenology research method was applied in this study. Data was collected by participants drawings and tape-recorded interviews. The data was analyzed by the procedure of Colaizzi phenomenological methodology. The rigor of this study was further examined using Lincoln and Guba (1985) principles. Results: The participants of this study consisted of 10 adolescent with bone cancer who having been received orthopedic surgery. Four major themes were found which including the inspiration of meaningful goals, the development of disease coping strategies; the power of caring and encouragement; and faith and positive momentum. Conclusion: The study findings may provide evidence-based information for nurses in caring for adolescent bone cancer patients during their disease treatment. Key Words: Bone Cancer, Adolescents, Hope, Drawings