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      The experience of family caregivers of patients with cancer in an Asian country: A grounded theory approach

      1 , 2 , 2 , 3 , 1 , 4
      Palliative Medicine
      SAGE Publications

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          Abstract

          Background:

          Strong family bonds are part of the Indonesian culture. Family members of patients with cancer are intensively involved in caring, also in hospitals. This is considered “normal”: a societal and religious obligation. The values underpinning this might influence families’ perception of it.

          Aim:

          To explore and model experiences of family caregivers of patients with cancer in Indonesia in performing caregiving tasks.

          Design:

          A grounded theory approach was applied. The constant comparative method was used for data analysis and a paradigm scheme was employed for developing a theoretical model.

          Setting/participants:

          The study was conducted in three hospitals in Indonesia. The participants were family caregivers of patients with cancer.

          Results:

          A total of 24 family caregivers participated. “Belief in caregiving” appeared to be the core phenomenon. This reflects the caregivers’ conviction that providing care is an important value, which becomes the will power and source of their strength. It is a combination of spiritual and religious, value and motivation to care, and is influenced by contextual factors. It influences actions: coping mechanisms, sharing tasks, and making sacrifices. Social support influences the process of the core phenomenon and the actions of the caregivers. Both positive and negative experiences were identified.

          Conclusion:

          We developed a model of family caregivers’ experiences from a country where caregiving is deeply rooted in religion and culture. The model might also be useful in other cultural contexts. Our model shows that the spiritual domain, not only for the patient but also for the family caregivers, should be structurally addressed by professional caregivers.

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          Most cited references35

          • Record: found
          • Abstract: found
          • Article: not found

          The cancer family caregiving experience: an updated and expanded conceptual model.

          The decade from 2000 to 2010 was an era of tremendous growth in family caregiving research specific to the cancer population. This research has implications for how cancer family caregiving is conceptualized, yet the most recent comprehensive model of cancer family caregiving was published ten years ago. Our objective was to develop an updated and expanded comprehensive model of the cancer family caregiving experience, derived from concepts and variables used in research during the past ten years. A conceptual model was developed based on cancer family caregiving research published from 2000 to 2010. Our updated and expanded model has three main elements: 1) the stress process, 2) contextual factors, and 3) the cancer trajectory. Emerging ways of conceptualizing the relationships between and within model elements are addressed, as well as an emerging focus on caregiver-patient dyads as the unit of analysis. Cancer family caregiving research has grown dramatically since 2000 resulting in a greatly expanded conceptual landscape. This updated and expanded model of the cancer family caregiving experience synthesizes the conceptual implications of an international body of work and demonstrates tremendous progress in how cancer family caregiving research is conceptualized. Copyright © 2011 Elsevier Ltd. All rights reserved.
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            Exploring the spiritual needs of people dying of lung cancer or heart failure: a prospective qualitative interview study of patients and their carers

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              • Record: found
              • Abstract: found
              • Article: not found

              Cancer and caregiving: the impact on the caregiver's health.

              A diagnosis of cancer affects not only the patient but also their significant others, especially when a lot of care tasks are involved. Some caregivers perceive the care as a burden, while others consider it a challenge. In this article, findings concerning the impact of cancer caregiving on informal caregivers will be described. No consistent results are reported, and little is known about patterns of caregiving changes in relation to the course of the patient's illness. Attention will be given to factors which have been identified as influencing the course and consequences of caregiving. These factors form the basis of a conceptual research model for caregivers of cancer patients. As cancer progresses, care tasks are generated, which can be perceived by the caregiver as either negative (i.e. burden) or positive. Furthermore, these caregiver experiences may lead to negative as well as positive effects on the caregiver's health and these relationships can be assumed to be bidirectional.
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                Author and article information

                Journal
                Palliative Medicine
                Palliat Med
                SAGE Publications
                0269-2163
                1477-030X
                April 10 2019
                June 2019
                March 27 2019
                June 2019
                : 33
                : 6
                : 676-684
                Affiliations
                [1 ]Radboud University Medical Center, IQ Healthcare, Nijmegen, The Netherlands
                [2 ]School of Nursing, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia
                [3 ]Department of Health Policy and Management, Universitas Gadjah Mada, Yogyakarta, Indonesia
                [4 ]Department of Anesthesiology, Pain and Palliative Medicine, Radboud University Medical Center, Nijmegen, The Netherlands
                Article
                10.1177/0269216319833260
                30916614
                6b5fd8f5-0522-4025-a98f-14a79758a59e
                © 2019

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