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      Health literacy and its association with mental and spiritual well-being among women experiencing homelessness

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          Abstract

          Low health literacy (HL) has been linked to low self-rated health, reduced efficacy of behaviour change, and challenges in preventing, treating, or managing health conditions. People experiencing homelessness are at risk of poor HL; however, few studies have investigated HL in relation to mental and spiritual well-being among people experiencing homelessness in general, or women experiencing homelessness specifically. This cross-sectional study of 46 women experiencing homelessness in Stockholm, Sweden, recruited during the period October 2019–December 2020, aimed to examine how HL was associated with mental and spiritual well-being among women experiencing homelessness. Participants answered questions about socio-demographic characteristics (age, length of homelessness, education) and digital technology (mobile phone/the Internet) use, in addition to Swedish language versions of three questionnaires administered through structured, face-to-face interviews: the Communicative and Critical Health Literacy Scale, the General Health Questionnaire 12 and the Functional Assessment of Chronic Illness Therapy-Spiritual Well-Being. Data were analysed using linear regression, which revealed statistically significant associations between HL and mental well-being ( p = .009), and between HL and spiritual well-being ( p = .022). However, neither socio-demographic characteristics nor digital technology use were significantly associated with HL. In conclusion, promoting HL may improve mental and spiritual well-being in this vulnerable population. An advisory board of women with lived experiences of homelessness ( n = 5) supported the interpretation of the findings and emphasised the need to consider HL in relation to basic needs such as ‘housing first’. Moreover, health information and services should be accessible to people with different degrees of HL.

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          The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies.

          Much of biomedical research is observational. The reporting of such research is often inadequate, which hampers the assessment of its strengths and weaknesses and of a study's generalizability. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Initiative developed recommendations on what should be included in an accurate and complete report of an observational study. We defined the scope of the recommendations to cover three main study designs: cohort, case-control, and cross-sectional studies. We convened a 2-day workshop in September 2004, with methodologists, researchers, and journal editors to draft a checklist of items. This list was subsequently revised during several meetings of the coordinating group and in e-mail discussions with the larger group of STROBE contributors, taking into account empirical evidence and methodological considerations. The workshop and the subsequent iterative process of consultation and revision resulted in a checklist of 22 items (the STROBE Statement) that relate to the title, abstract, introduction, methods, results, and discussion sections of articles. Eighteen items are common to all three study designs and four are specific for cohort, case-control, or cross-sectional studies. A detailed Explanation and Elaboration document is published separately and is freely available on the web sites of PLoS Medicine, Annals of Internal Medicine, and Epidemiology. We hope that the STROBE Statement will contribute to improving the quality of reporting of observational studies.
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            World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects.

            (2014)
            Published research in English-language journals are increasingly required to carry a statement that the study has been approved and monitored by an Institutional Review Board in conformance with 45 CFR 46 standards if the study was conducted in the United States. Alternative language attesting conformity with the Helsinki Declaration is often included when the research was conducted in Europe or elsewhere. The Helsinki Declaration was created by the World Medical Association in 1964 (ten years before the Belmont Report) and has been amended several times. The Helsinki Declaration differs from its American version in several respects, the most significant of which is that it was developed by and for physicians. The term "patient" appears in many places where we would expect to see "subject." It is stated in several places that physicians must either conduct or have supervisory control of the research. The dual role of the physician-researcher is acknowledged, but it is made clear that the role of healer takes precedence over that of scientist. In the United States, the federal government developed and enforces regulations on researcher; in the rest of the world, the profession, or a significant part of it, took the initiative in defining and promoting good research practice, and governments in many countries have worked to harmonize their standards along these lines. The Helsinki Declaration is based less on key philosophical principles and more on prescriptive statements. Although there is significant overlap between the Belmont and the Helsinki guidelines, the latter extends much further into research design and publication. Elements in a research protocol, use of placebos, and obligation to enroll trials in public registries (to ensure that negative findings are not buried), and requirements to share findings with the research and professional communities are included in the Helsinki Declaration. As a practical matter, these are often part of the work of American IRBs, but not always as a formal requirement. Reflecting the socialist nature of many European counties, there is a requirement that provision be made for patients to be made whole regardless of the outcomes of the trial or if they happened to have been randomized to a control group that did not enjoy the benefits of a successful experimental intervention.
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              The health of homeless people in high-income countries: descriptive epidemiology, health consequences, and clinical and policy recommendations.

              In the European Union, more than 400,000 individuals are homeless on any one night and more than 600,000 are homeless in the USA. The causes of homelessness are an interaction between individual and structural factors. Individual factors include poverty, family problems, and mental health and substance misuse problems. The availability of low-cost housing is thought to be the most important structural determinant for homelessness. Homeless people have higher rates of premature mortality than the rest of the population, especially from suicide and unintentional injuries, and an increased prevalence of a range of infectious diseases, mental disorders, and substance misuse. High rates of non-communicable diseases have also been described with evidence of accelerated ageing. Although engagement with health services and adherence to treatments is often compromised, homeless people typically attend the emergency department more often than non-homeless people. We discuss several recommendations to improve the surveillance of morbidity and mortality in homeless people. Programmes focused on high-risk groups, such as individuals leaving prisons, psychiatric hospitals, and the child welfare system, and the introduction of national and state-wide plans that target homeless people are likely to improve outcomes.
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                Author and article information

                Contributors
                Journal
                Health Promot Int
                Health Promot Int
                heapro
                Health Promotion International
                Oxford University Press (US )
                0957-4824
                1460-2245
                April 2024
                02 March 2024
                02 March 2024
                : 39
                : 2
                : daae019
                Affiliations
                Department of Statistics, Uppsala University , Box 513, 751 20, Uppsala, Sweden
                Department of Medical Sciences, Division of Clinical Diabetology and Metabolism, Uppsala University , Akademiska sjukhuset, 751 85, Uppsala, Sweden
                Department of Neurobiology, Care Sciences and Society, Division of Family Medicine and Primary Care, Karolinska Institutet , 171 77, Stockholm, Sweden
                Department of Women’s and Children’s Health, Healthcare Services and e-Health, Uppsala University , Akademiska sjukhuset, 751 85, Uppsala, Sweden
                Department of Healthcare Sciences, Marie Cederschiöld University , Box 11189, 100 61, Stockholm, Sweden
                Division of Psychiatry, Faculty of Brain Sciences, University College London , Maple House, W1T 7BN, London, UK
                Department of Women’s and Children’s Health, Healthcare Services and e-Health, Uppsala University , Akademiska sjukhuset, 751 85, Uppsala, Sweden
                Department of Healthcare Sciences, Marie Cederschiöld University , Box 11189, 100 61, Stockholm, Sweden
                Department of Women’s and Children’s Health, Healthcare Services and e-Health, Uppsala University , Akademiska sjukhuset, 751 85, Uppsala, Sweden
                Department of Healthcare Sciences, Marie Cederschiöld University , Box 11189, 100 61, Stockholm, Sweden
                Department of Healthcare Sciences, Marie Cederschiöld University , Box 11189, 100 61, Stockholm, Sweden
                Author notes
                Author information
                https://orcid.org/0000-0003-3691-8326
                https://orcid.org/0000-0001-7935-3260
                https://orcid.org/0000-0003-0479-6950
                https://orcid.org/0000-0001-5104-1281
                https://orcid.org/0000-0001-5804-0433
                Article
                daae019
                10.1093/heapro/daae019
                10908353
                38430507
                95b5e42a-9115-455c-b60f-7bbc9a8f7e4a
                © The Author(s) 2024. Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                Page count
                Pages: 12
                Funding
                Funded by: Swedish Research Council (Vetenskapsrådet);
                Award ID: 2019-01095
                Funded by: Research Council on Health, Working Life and Welfare, FORTE (Forskningsrådet för hälsa, arbetsliv och välfärd);
                Award ID: 2020-00169
                Categories
                Article
                Health Literacy
                AcademicSubjects/MED00860

                Public health
                health literacy,homelessness,psychological distress,spirituality,psychological well-being,women’s health

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