| 168 20. Lim J, Goh J, Chionh HL, Yap P. Why do patients and their families not use services for dementia? Perspectives from a developed Asian country. International Psychogeriatrics. 2012;24(10):1571-80. 21. Langdon SA, Eagle A, Warner J. Making sense of dementia in the social world: A qualitative study. Social Science & Medicine. 2007;64(4):989-1000. 22. Bergmann S, Peper J, Bieber A. The use of formal care for dementia from a professional perspective: a scoping review. BMC Health Services Research. 2022;22(1):825. 23. Gibson AK, Anderson KA. Difficult Diagnoses: Family Caregivers’ Experiences During and Following the Diagnostic Process for Dementia. American Journal of Alzheimer’s Disease & Other Dementias. 2011;26(3):212-7. 24. Boots LM, Wolfs CA, Verhey FR, Kempen GI, de Vugt ME. Qualitative study on needs and wishes of early-stage dementia caregivers: the paradox between needing and accepting help. Int Psychogeriatr. 2015;27(6):927-36. 25. Vinay R, Biller-Andorno N. A critical analysis of national dementia care guidances. Health Policy. 2023;130:104736. 26. Fortinsky RH, Downs M. Optimizing Person-Centered Transitions In The Dementia Journey: A Comparison Of National Dementia Strategies. Health Affairs. 2014;33(4):566-73. 27. Australian Government Department of Health and Aged Care. National Dementia Action Plan Public Consultation Paper. 2022. 28. Huijsman R, Boomstra R, Veerbeek M, Döpp C. Zorgstandaard Dementie 20202020 2020. 67 p. 29. A Dementia Strategy for Canada: Together We Aspire. Publich Health agency of Canada; 2019 2019-06-17. Report No.: 978-0-660-31210-1. 30. Alzheimer Wielkopolska. Jak pomagamy [cited 2023 01/09/2023]. Available from: https:// alzheimerwielkopolska.pl/dzialalnosc/jak-pomagamy/. 31. Kerpershoek L, Wolfs C, Verhey F, Jelley H, Woods B, Bieber A, et al. Optimizing access to and use of formal dementia care: Qualitative findings from the European Actifcare study. Health & Social Care in the Community. 2019;27(5):e814-e23. 32. Brooke J, Cronin C, Stiell M, Ojo O. The intersection of culture in the provision of dementia care: A systematic review. Journal of Clinical Nursing. 2018;27(17-18):3241-53. 33. Szcześniak D, Rymaszewska J, Saibene FL, Lion KM, D’arma A, Brooker D, et al. Meeting centres support programme highly appreciated by people with dementia and carers: a European crosscountry evaluation. Aging & Mental Health. 2021;25(1):149-59. 34. James T, Mukadam N, Sommerlad A, Barrera-Caballero S, Livingston G. Equity in care and support provision for people affected by dementia: experiences of people from UK South Asian and White British backgrounds. International Psychogeriatrics. 2023:1-10. 35. Tong A, Sainsbury P, Craig J. Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups. International Journal for Quality in Health Care. 2007;19(6):349-57. 36. Hevink M, Wolfs C, Ponds R, Doucet S, McAiney C, Vedel I, et al. Experiences of people with dementia and informal caregivers with post-diagnostic support: Data from the international COGNISANCE study. International Journal of Geriatric Psychiatry. 2023;38(5):e5916. 37. World Medical Association. World Medical Association Declaration of Helsinki. Ethical principles for medical research involving human subjects. Bulletin of the World Health Organization. 2001;79(4):373-4. 38. Archibald MM, Ambagtsheer RC, Casey MG, Lawless M. Using Zoom Videoconferencing for Qualitative Data Collection: Perceptions and Experiences of Researchers and Participants. International Journal of Qualitative Methods. 2019;18:1609406919874596. 39. Jayasekara RS. Focus groups in nursing research: Methodological perspectives. Nursing Outlook. 2012;60(6):411-6.
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