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The purpose of this research is to determine if it is advantageous to employ electronic home monitoring (EHM) for heart failure patients. Advantageous is determined by whether or not additional costs and hospital visits could be reduced with this technology, and if it could increase the length of time between hospital visits.
The research questions in this study were implicit and stated in the form of three hypotheses. The first questioned whether or not lower costs, emergency room and hospital visits could be achieved with EHM, the second was whether or not quality of life and caregiver mastery could improve while lowering rates of depressive symptoms, and the final one wondered whether or not, the combination of EHM, caregiver mastery and informal social support could decrease the risk of readmission to hospitals.
The authors provided a lengthy description of the design of this study which involved a randomized clinical trial in which there was a control group and an intervention group, the latter of which utilized EHM. The researchers attempted to make all other factors equal between these groups, including facets related to their sample pool.
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Caregiver Burnout and Compassion Fatigue Caregiver Compassion Fatigue Those who care for others as part of their professional duties must understand the nature of caregiver fatigue and the basics of caring for oneself. Generally, the focus of a caregiver remains on the care recipient to such a degree that personal limitations are ignored and self-care principles are shunted to the background. Caregivers rarely have realistic expectations about the long-term impact of caregiving,
Caregiver Interview as Related to Physical Therapy The objective of this study is to determine what types of psychosocial issues arise for individuals who render primary care to a PWD on a routine basis, and to determine how these caregivers cope with the stress of their responsibilities. This will involve an interview. The interview in this study is conducted with a woman who will be known in this study as Karen Hill,
Caregivers of individuals with AD Caregivers of Individuals with Alzheimer's Disease Alzheimer's disease is a terribly debilitating disease that strikes older adults and for which there is no known cure. According to the Institute on Aging, Alzheimer's disease is "an irreversible, progressive brain disease that slowly destroys memory and thinking skills, and eventually even the ability to carry out the simplest tasks." (2012, p.1) Alzheimer's disease is named after Dr. Alois Alzheimer.
There are certainly different approaches to the theory of anticipatory mourning. Clearly, one of the major issues within the literature surrounds the communication between the dying person and the caregiver, and both caregiver and patient and those who will be most affected or will mourn their loss. Conventional theory finds that preparing for loss involves experiencing most of the features of grief prior to the demise of the patient; numbness,
caregivers of those with dementia through a structure process of information giving. The goal is to determine specifically what information those that care for people with dementia want at the time of diagnosis. It is also necessary to examine the discrepancies between the information that these individuals receive and the information that they actually need to care for the individual in the best way possible. The primary question dealt
caregivers face when it comes to differentiating between dementia, delirium, and depression due to overlap of depression and delirium in older people. Some symptoms that accompany depression are also pronounced in dementia (Peacock, Hopton, Featherstone & Jill, 2012). These include withdrawal and sleepiness. This overlap creates some problem when it comes to differentiating the two. Problem in this study and the purpose for which it was commissioned is clearly stated.
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