National Repository of Grey Literature 6 records found  Search took 0.00 seconds. 
Communication disorders of people with Alzheimer's disease
Bláhová, Natálie ; Korandová, Zuzana (advisor) ; Horynová, Jana (referee)
The topic of the thesis Communication disorders of people with Alzhiemer's disease is focused on the analysis of the manifestations of impaired communication ability of people with Alzheimer's disease. The bachelor thesis is divided into theoretical and practical part. The theoretical part consists of two chapters. In the firts chapter, entitled Theoretical Background, the term communication is discussed, as well as the concept of dementia. Other subsections discuss cognitive-communication disorders and manifestiations of impaired communication ability of people with dementia. Speech and language process deficits in individual language levels are also listed here. The second chapter deals with neurodegenerative disease. It is followed by a subchapter related to Alzheimer's disease and subsequently clarifies the topic of the burden placed on family caregivers. The practical part presents an analysis of a research investigation that was carried out in the Clementas home for the elderly in Janovice nad Úhlavou. A presentation of the Clementas Center is also included in the bachelor's thesis. The research sample consisted of tree clients of this home. The practical part was based on observing the participants, using indicative diagnostic tools and the clients' health documentation. Furthermore, the...
The Support of family carers ( experience from Diaconia ECCB courses - Take care at home)
Lengálová, Michaela ; Janečková, Hana (advisor) ; Čížková, Hana (referee)
Caring for a loved one is nothing new in our contemporary society. We deal with the topics of caring in the family, the motivation of such a decision, the positives or negatives of this choice. Why do more and more people choose to care for a loved one "at home"? What is the state support provided to family carers and which social policy instruments does the state use? The aim of the Diakonie ČCE-Care at Home project is to comprehensively support lay family caregivers who take care of their loved ones, not only the elderly, people with disabilities, children with disabilities, but also cancer patients. Through information, counseling and educational activities, we provide family caregivers with the psycho-social and spiritual support they need when caring for their loved ones. Not only do the people receiving care in the home environment have their own needs, but so do family caregivers, whose way of saturating their needs changes the moment they begin caregiving. In general, we are concerned with the needs and their fulfilment of the patients themselves, i.e. those who are dependent on care. But we must not neglect family caregivers, since their physical and mental well-being is a prerequisite for being able to care for their loved ones because they have a very difficult task ahead of them, which...
Family Needs of Patients after Cerebral Impairment
BÁRTOVÁ, Marie
The thesis is a part of the project called Coordinated rehabilitation of the patients with the brain injury (reg. n. GAJU 138/20146/S). The objective of this work is to find out what needs the families of patients with the brain injury have. This thesis has a theoretical and a practical part. According to research set consisting of 14 caregivers of patients after cerebrovascular accident and only one that cares about a patient after cranial trauma, the theoretical part describes a CMP characteristic, coordinated rehabilitation, the basic terms about family and the chosen concepts of needs. Based on the objective of the thesis, the research question was stated: What are the needs of family members who care about the patients with the brain injury in the home environment? The research was made by the qualitative strategy and the semi-structured interviews with the family members in South Bohemia region who cares about the people with the brain injury in the home environment. It was important that people with the brain injury have already been joined to the project. The interviews were done in the application called Atlas.ti. According to the analysis of the collected data, there are 9 main needs that are connected to each other. Concretely, it is a need of a care about the patient, about the house, the need of a family help, the need of professional and social services, economic security and quicker help by the social service, furthermore the need of free time, psychological well-being and being in touch with the society. The results of this thesis are a part of the complex results of the project GAJU called Coordinated rehabilitation of patients with the brain injury (ref. n. GAJU 138/20146/S). The analysis of the needs of family members was used to propose the solutions/saturation of the needs in order to influence the real life of interviewers.
Alzheimer's Disease and Family Caregiver Burden. Impact of Alzheimer's Disease on Family Caregiver Psychosocial Health.
Zvěřová, Martina ; Jirák, Roman (advisor) ; Holmerová, Iva (referee) ; Zvolský, Petr (referee)
Alzheimer's Disease is a progressive, irreversible neurodegenerative illness and the most common of the dementing disorders. Only few diseases disrupt patients and their relatives so completely or for so long a period of time as Alzheimer 's. Caring is held to be very demanding and emotionally involving. Caregiver burden has been defined as a multidimensional response to emotional, social, physical, psychological, and financial stressors associated with the caregiving experience. The objective of the 1st study was to assess the degree of burden and its possible change in family caregivers of the long-term sick family member with progressive Alzheimer's disease during eight-month monitoring. In addition to the common psychiatric examination the Mini- Mental State Examination (MMSE) was administered in patients to indicate the severity of the dementia and the Zarit Burden Interview was administered in caregivers to assessed degree of burden. The total of 60 people have been examined - 30 patients with AD and 30 their caregivers (24 females, 6 males) were recruited from the Department of Psychiatry, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague. At the beginning of the study there were 18 patients with mild stage of AD (60%), 11 patients suffered...
Family Needs In the Context of Care for Seriously Ill Elderly
OKTÁBCOVÁ, Denisa
This bachelor publication is consists of theoretical and empirical part. The theoretical part is about home care, which is focuse for seniors who needs a long time care. In the publication is a mentioned chapter, which is dedicating the problematic of ballast the family caregivers. And in this chapter is a part with theirs needs. After introduction the chosen illness which are directly related with the issue of old age is pointed out on sick seniors too. Including general family caregivers. And then is seen into the present situation of intergenerational live between seniors and one or more ranks of younger generation. In connection with family caregivers needs is necessarily in this project say something about the organizations, which have in the case of interes tor necessity help to caregiver. In the empirical part is qualitative research, which is made of semi structured interview with ten informants, who currently care for a sick old human in a common household in south Bohemia region. The research sample was created by "snowball sampling." After a theoretical description selected strategy, technics, method and selective sample, follows the research indeed. A primary objective is an evaluation the changing roles of family caregiver when they began care about him. A secondary objectives are a finding an availability of formal and informal help firstly and the finding a interest of family about using many forms of help secondly. Research questions are focuses on changes, which have occurred on a carer, type of help, which is the most beneficial and finally for a human, who asking for help. Research results showed the role change of family caregiver in the free time activities and jobs due better joint about care and work responsibilities. A job can serve like a reason to mean for family, who decided between an institutional and home care for seniors, if considering a negatives and positives of it. At the same time can provide a moral support to the pupil, who already do a home caregiver for a sick senior.

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