References 
World Health Organization, (2021). Global status report on the public health response to dementia. 
Al-Qusous, D., (2025). Enhancing Dementia Care through Interior Design: Cultural Adaptation and Modification of Environments in the Middle East-North African Region.
Chen, M.C. and Lin, H.R., (2022). The experiences of family caregivers in response to a dementia diagnosis disclosure. BMC psychiatry, 22(1), p.475.
Cleveland Clinic (2023). Caregiver burnout. [Online] Available at: https://my.clevelandclinic.org/health/diseases/9225-caregiver-burnout.  (Accessed on:  06.11.2025) 
Cruise, C.E. and Lashewicz, B.M., (2022). Dementia and dignity of identity: A qualitative evidence synthesis. Dementia, 21(4), pp.1233-1249.
Daly, R. and Drain, D. (2024). Psychosocial interventions in palliative and end-of-life care | Nursing Times. [Online] Available at: https://www.nursingtimes.net/end-of-life-and-palliative-care/psychosocial-interventions-in-palliative-and-end-of-life-care-18-11-2024/. (Accessed on:  06.11.2025) 
Festen, S., van Twisk, Y.Z., van Munster, B.C. and de Graeff, P., (2021). ‘What matters to you?’Health outcome prioritisation in treatment decision-making for older patients. Age and Ageing, 50(6), pp.2264-2269.
Guzzon, A., Rebba, V., Paccagnella, O., Rigon, M. and Boniolo, G., (2023). The value of supportive care: A systematic review of cost-effectiveness of non-pharmacological interventions for dementia. PLoS One, 18(5), p.e0285305.
Hoare, J., (2023). The power of connected clinical teams: from loneliness to belonging. Philosophy, Ethics, and Humanities in Medicine, 18(1), p.16.
Jahangir, S., Patil, D.S., Gangopadhyay, J. and Vogt, T.C., (2025). Understanding intergenerational dynamics and social support’s impact on health and well-being of older adults in South Asia: a scoping review. Systematic Reviews, 14(1), p.86.
‌Kelley, R., Godfrey, M. and Young, J., (2019). The impacts of family involvement on general hospital care experiences for people living with dementia: an ethnographic study. International journal of nursing studies, 96, pp.72-81.
Lee, J., Baik, S., Becker, T.D. and Cheon, J.H., (2022). Themes describing social isolation in family caregivers of people living with dementia: A scoping review. Dementia, 21(2), pp.701-721. 
Lillekroken, D., Halvorsrud, L., Bjørge, H., Gandhi, S., Sivakumar, P.T. and Goyal, A.R., (2024). Caregivers’ experiences, challenges, and needs in caring for people with dementia in India: a scoping review. BMC Health Services Research, 24(1), p.1661.
Nandi, A., Counts, N., Bröker, J., Malik, S., Chen, S., Han, R., Klusty, J., Seligman, B., Tortorice, D., Vigo, D. and Bloom, D.E., (2024). Cost of care for Alzheimer’s disease and related dementias in the United States: 2016 to 2060. npj Aging, 10(1), p.13. 
Sailian, S.D., Salifu, Y. and Preston, N., (2025). Family caregivers’ role in dignity: A qualitative study can we change the title to: Dignity in Serious Illness: A Qualitative Exploration of Family Caregivers’ Contributions in low middle-income country. Palliative & supportive care, 23, p.e61. 
Sunjaya, A.M., Schreiber, T., Kantilal, K., Davies, N. and Griffiths, S., (2025). Communication strategies for delivering personalised dementia care and support: a mixed-methods systematic review and narrative synthesis. Age and Ageing, 54(5), p.afaf120.