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Health Care Provision to Transgender Individuals; Understanding Clinician Attitudes and Knowledge AcquisitionKline, Leo Isaac 01 January 2015 (has links)
The Institute of Medicine report of 2011 defined Transgender Specific Health Needs as one of four priority research areas. While there is research asserting that health care providers (HCPs) do not have adequate training in providing competent care to transgender patients, there are no studies to date assessing HCPs' gender identity attitudes and their willingness to learn the Standards of Care (SOC) developed for this patient population. According to the Agency for Health Care Research and Quality, as of 2010, 52% of Nurse Practitioners (NPs) were practicing in primary care settings. As more than half of NPs practice in primary care and transgender patients often initially present their gender concerns to their primary care provider, this study focuses on the NP population.
This study describes a sample of NPs' attitudes towards gender variance, as well as their perceived need and interest in learning the SOC as published by the World Professional Association for Transgender Health. Multi-state purposive sampling of NP professional organizations was conducted. Two conservative and two progressive states' professional organizations were included in the sample. The states were randomly assigned within both geopolitical groups to intervention or control with the use of a random numbers table.
Comparisons between geopolitical groups and between control and intervention groups cannot be made due to low response rates of all states. The majority of this small sample of NPs agreed that they needed and wanted additional training in transgender health care. Future research with representative sample sizes is needed to better understand provider-sided barriers to caring for this marginalized patient population.
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Quality of Life and Barriers to Health Care of Prostate Cancer Survivors Residing in Gaza StripAbu-El-Noor, Nasser I. 06 August 2010 (has links)
No description available.
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Barriers to Native American Women Veterans’ Health Care Access on TwoReservations: Northern Cheyenne and FlatheadAl Masarweh, Luma Issa 01 July 2014 (has links) (PDF)
Little research has addressed the needs of Native American veterans. This study aims to provide a better understanding of Native American women veterans’ experiences using data from the Veteran Administration and Indian Health Services. Fifteen interviews were conducted with special attention to quality and quantity of health and mental health care services available to veterans, the barriers and local contextual factors in accessing and utilizing services, and potential solutions to service gaps for women veterans from two Montana reservations, the Northern Cheyenne and Flathead Confederated Salish and Kootenai Tribes. American Indians and Alaska Natives serve at a higher rate in the U.S military than any other population. Native American women veterans identified many barriers to accessing care, some of which include lack of information regarding eligibility and the type of services available. Many found the application process to be confusing and difficult. Other barriers included distance, cost of travel, and conflict with their work schedule. This research provides important data about Native American veterans who are often underrepresented in survey research and are a rapidly growing segment of the United States military and veteran population.
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Dostupnost zdravotní péče pro migranty ze třetích zemí v České republice / Access to healthcare for third countries migrants in the Czech RepublicDobiášová, Karolína January 2016 (has links)
This Ph.D. thesis discusses the evolution and current situation regarding availability of healthcare for third countries migrants in the Czech Republic. In terms of methodology, the author has chosen a qualitative approach. The research design is a historical case study. The thesis uses a combination of "desk research" and empirical survey based on 56 in-depth interviews with migrants, healthcare providers and experts who come into contact with migrants during the course of their work. Based on the approach of historical institutionalism, the author is explaining policy of migrants' health insurance evolution in Czech Republic since 1993 till today. The author identifies the key events and the roles of particular actors within the observed "sub- system" of public policy. From the viewpoint of migrants and healthcare providers, the thesis also presents how the current institutionalised set-up of migrants' health policy transfers into the real access to healthcare for migrants. It also identifies the main barriers to health care accessibility and the consequences of possible health care unavailability. Key words: migrants, health care availability, health insurance, historical institutionalism, barriers to health care access
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