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dc.contributor.authorHeaslip, Vanessa
dc.contributor.authorGreen, Sue
dc.contributor.authorSimkhada, Bibha
dc.contributor.authorDogan, Huseyin
dc.contributor.authorRicher, Stephen
dc.date.accessioned2022-07-13T13:00:35Z
dc.date.available2022-07-13T13:00:35Z
dc.date.created2022-05-09T11:06:14Z
dc.date.issued2021-12
dc.identifier.citationHeaslip, V., Green, S., Simkhada, B., Dogan, H., & Richer, S. (2021). How Do People Who Are Homeless Find Out about Local Health and Social Care Services: A Mixed Method Study. International Journal of Environmental Research and Public Health, 19(1), 46.en_US
dc.identifier.issn1661-7827
dc.identifier.urihttps://hdl.handle.net/11250/3005081
dc.description.abstractBackground: There are significant numbers of people experiencing homelessness both in the UK and internationally. People who are homeless are much more likely to die prematurely and, therefore, need strong access to ongoing health and social care support if we hope to address the health disparity they face. Objectives: The aim of the research was to explore how people who are homeless identify and locate appropriate health and social care services. Design: A mixed methods research study was applied on people who are currently homeless or had previously experienced homelessness. Settings: The research study was based in an urban area in the southwest of England. The area was chosen as it was identified to be in the top 24 local authorities for the number of homeless individuals. Participants: A hundred individuals participated in the survey, of those 32% were living on the streets whilst 68% were living in temporary accommodation such as a charity home, shelter or a hotel paid for by the local authority. In addition, 16 participated in either a focus group or one-to-one interview Methods: The quantitative component consisted of a paper-based questionnaire whilst the qualitative aspect was focus groups/one-to-one interviews. The COREQ criteria were used in the report of the qualitative aspects of the study. Results: Quantitative data identified poor health in 90% of the sample. Access to both healthcare and wider wellbeing services (housing and food) was problematic and support for this was largely through third sector charity organisations. Qualitative data identified numerous systemic, individual and cultural obstacles, leaving difficulty for people in terms of knowing who to contact and how to access services, largely relying on word of mouth of other people who are homeless. Conclusions: In order to address health inequities experienced by people who are homeless, there is a need to review how information regarding local health and wider wellbeing services is provided in local communities.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjecthjemløsheten_US
dc.subjectsosial ekskluderingen_US
dc.subjectmental helseen_US
dc.subjectpsykisk helseen_US
dc.subjectteknologien_US
dc.titleHow do people who are homeless find out about local health and social care services: A mixed method studyen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2021 by the authorsen_US
dc.subject.nsiVDP::Samfunnsvitenskap: 200::Sosialt arbeid: 360en_US
dc.subject.nsiVDP::Medisinske Fag: 700::Helsefag: 800en_US
dc.source.volume19en_US
dc.source.journalInternational Journal of Environmental Research and Public Health (IJERPH)en_US
dc.source.issue1en_US
dc.identifier.doi10.3390/ijerph19010046
dc.identifier.cristin2022589
dc.source.articlenumber46en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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