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1.
Patient Educ Couns ; 116: 107932, 2023 11.
Artigo em Inglês | MEDLINE | ID: mdl-37566948

RESUMO

OBJECTIVES: Patient education and health literacy aim to enhance understanding of health and self-care for optimal health outcomes. However, the attention towards populations with visual impairments requiring specialized accommodations for improved health literacy and healthcare access appears to be insufficient METHODS: In an effort to bridge this gap, we conducted a scoping review focusing on health literacy studies undertaken specifically for individuals with visual impairments. RESULTS: We encapsulate the main findings and constraints of preceding studies and deliberate on the influence of health literacy research for individuals with visual impairments on healthcare inequalities and health disparities. CONCLUSIONS: A health-literate approach, combined with an accessible healthcare environment, can serve as a catalyst to motivate individuals with visual impairments to actively engage in their self-care practices. PRACTICE IMPLICATIONS: It is of utmost urgency to develop and validate a health literacy assessment tool for visually impaired individuals, and to utilize it for providing healthcare interventions as well as health education.


Assuntos
Letramento em Saúde , Humanos , Acessibilidade aos Serviços de Saúde , Disparidades em Assistência à Saúde , Educação em Saúde , Transtornos da Visão/terapia
2.
J Med Internet Res ; 25: e43917, 2023 05 04.
Artigo em Inglês | MEDLINE | ID: mdl-37140967

RESUMO

BACKGROUND: Personal health technologies, including wearable tracking devices and mobile apps, have great potential to equip the general population with the ability to monitor and manage their health. However, being designed for sighted people, much of their functionality is largely inaccessible to the blind and low-vision (BLV) population, threatening the equitable access to personal health data (PHD) and health care services. OBJECTIVE: This study aims to understand why and how BLV people collect and use their PHD and the obstacles they face in doing so. Such knowledge can inform accessibility researchers and technology companies of the unique self-tracking needs and accessibility challenges that BLV people experience. METHODS: We conducted a web-based and phone survey with 156 BLV people. We reported on quantitative and qualitative findings regarding their PHD tracking practices, needs, accessibility barriers, and work-arounds. RESULTS: BLV respondents had strong desires and needs to track PHD, and many of them were already tracking their data despite many hurdles. Popular tracking items (ie, exercise, weight, sleep, and food) and the reasons for tracking were similar to those of sighted people. BLV people, however, face many accessibility challenges throughout all phases of self-tracking, from identifying tracking tools to reviewing data. The main barriers our respondents experienced included suboptimal tracking experiences and insufficient benefits against the extended burden for BLV people. CONCLUSIONS: We reported the findings that contribute to an in-depth understanding of BLV people's motivations for PHD tracking, tracking practices, challenges, and work-arounds. Our findings suggest that various accessibility challenges hinder BLV individuals from effectively gaining the benefits of self-tracking technologies. On the basis of the findings, we discussed design opportunities and research areas to focus on making PHD tracking technologies accessible for all, including BLV people.


Assuntos
Dispositivos Eletrônicos Vestíveis , Humanos , Inquéritos e Questionários , Serviços de Saúde , Tecnologia Biomédica
3.
Ophthalmic Epidemiol ; 28(4): 277-284, 2021 08.
Artigo em Inglês | MEDLINE | ID: mdl-33380253

RESUMO

Purpose: Individuals with visual impairments and blindness who are marginalized in healthcare systems are located at the intersection of low accessibility for healthcare services and health-related information. To uncover recent trends in vision healthcare research, this study employed a text mining approach to literature analysis.Methods: A total of 506 journal articles published between January 2000 and April 2020 were collected from the Web of Science database. To investigate the main research themes and evolving trends, bibliometric and hierarchical cluster analyses were performed using R software.Results: Although the number of articles per year fluctuated in the past two decades, the findings of this study indicate a growing interest in visual impairment healthcare research. The United States contributed 32.3% to the overall output followed by the United Kingdom (16.7%). The prolific journals were Ophthalmic Epidemiology (4.7%), British Journal of Ophthalmology (4.4%), and JAMA Ophthalmology (3.4%). By using a hierarchical clustering algorithm, the 10 main research topics were estimated.Conclusions: Given the increasing prevalence of visual impairment in an aging society, an understanding of the current knowledge structure in scientific literature is essential for innovating on the existing healthcare system. The results of this study can guide researchers to discover the unexplored research areas and provide new directions for future work.


Assuntos
Bibliometria , Pesquisa sobre Serviços de Saúde , Cegueira/epidemiologia , Análise por Conglomerados , Humanos , Estados Unidos , Transtornos da Visão
4.
J Korean Acad Nurs ; 50(1): 132-146, 2020 Feb.
Artigo em Coreano | MEDLINE | ID: mdl-32131078

RESUMO

PURPOSE: The purpose of this study was to develop a new version of Spirituality Assessment Scale (N-SAS) and verify its reliability and validity. METHODS: The total of 59 preliminary items for the N-SAS were selected through a literature review, two rounds of experts' content validation, cognitive interviews, and pre-tests. Verification of its reliability and validity was divided into two phases. In Phase I, questionnaires were collected from 219 adults. Reliability was tested using Cronbach's alpha, validity with item analysis, and exploratory factor analysis. In Phase II, questionnaires developed based on the results of Phase I were collected from 225 adults. Reliability was tested using Cronbach's alpha, validity with confirmatory factor analysis, and criterion validity. RESULTS: The final version of the N-SAS comprised two dimensions (vertical and horizontal), four domains (relationship with God; meaning of life and self-integration; self-transcendence; and relationship with others, neighborhoods, and nature), and 44 items were identified. Total Cronbach's α was .97; those of each subscale ranged from .79 to .98. N-SAS scores were positively correlated with the scores of Howden's Spiritual Assessment Scale (r=.81, p<.001). CONCLUSION: Findings suggest that the N-SAS can be used to measure spirituality in adults. The use of N-SAS is expected to facilitate perceiving patient's spiritual needs and providing spiritual care.


Assuntos
Desenvolvimento de Programas , Avaliação de Programas e Projetos de Saúde , Espiritualidade , Adulto , Análise Fatorial , Feminino , Humanos , Entrevistas como Assunto , Masculino , Pessoa de Meia-Idade , Psicometria/métodos , Inquéritos e Questionários , Adulto Jovem
5.
Nurs Forum ; 54(2): 280-290, 2019 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-30737798

RESUMO

The inclusion of caregivers in a holistic care approach represents a basic principle in palliative care. However, many palliative care professionals have a lack of understanding of difficulties or unmet needs among caregivers. To enhance the quality of life of caregivers and the quality of care for patients, healthcare professionals should be better informed about the constructs of caregiver burden. The aim of this study is to synthesize the concept of caregiver burden in palliative care, providing implications for the caregivers and their support systems. This concept analysis study adopts the integrative review approach and the basic text analysis method (ie, word frequency). The PubMed, CINAHL, Embase, and PsycINFO databases are explored for eligible studies. From this literature search, 66 articles from 1998 to 2018 are located. After data collection is completed, the two authors independently evaluate the quality of studies published before 1 September 2018. The caregiver burden is then redefined with its attributes, antecedents, consequences, empirical referents, and facilitators. It is recommended that the multidimensional concept of caregiver burden in palliative care be measured by considering caregiver characteristics and the caregiving context.


Assuntos
Cuidadores/psicologia , Cuidados Paliativos/métodos , Qualidade de Vida , Adaptação Psicológica , Idoso , Idoso de 80 Anos ou mais , Cuidadores/economia , Formação de Conceito , Mineração de Dados , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Cuidados Paliativos/economia , Cuidados Paliativos/psicologia
6.
J Prev Med Public Health ; 46(3): 118-26, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23766869

RESUMO

We investigated the major trends in health aid financing in the Democratic People's Republic of Korea (DPRK) by identifying the primary donor organizations and examining several data sources to track overall health aid trends. We collected gross disbursements from bilateral donor countries and international organizations toward the DPRK according to specific health sectors by using the Organization for Economic Cooperation and Development creditor reporting system database and the United Nations Office for the Coordination of Humanitarian Affairs financial tracking service database. We analyzed sources of health aid to the DPRK from the Republic of Korea (ROK) using the official records from the ROK's Ministry of Unification. We identified the ROK, United Nations Children's Fund (UNICEF), World Health Organization (WHO), United Nations Population Fund (UNFPA), and The Global Fund to Fight AIDS, Tuberculosis and Malaria (GFATM) as the major donor entities not only according to their level of health aid expenditures but also their growing roles within the health sector of the DPRK. We found that health aid from the ROK is comprised of funding from the Inter-Korean Cooperation Fund, private organizations, local governments, and South Korean branches of international organizations such as WHO and UNICEF. We also distinguished medical equipment aid from developmental aid to show that the majority of health aid from the ROK was developmental aid. This study highlights the valuable role of the ROK in the flow of health aid to the DPRK, especially in light of the DPRK's precarious international status. Although global health aid from many international organizations has decreased, organizations such as GFATM and UNFPA continue to maintain their focus on reproductive health and infectious diseases.


Assuntos
Administração Financeira/economia , Bases de Dados Factuais , República Democrática Popular da Coreia , Equipamentos e Provisões Elétricas/economia , Equipamentos e Provisões Elétricas/estatística & dados numéricos , Administração Financeira/tendências , Gastos em Saúde/estatística & dados numéricos , Humanos , Nações Unidas , Organização Mundial da Saúde
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