“…As estimated, 75% of the patients with dementia are cared for by family caregivers (Li et al, 2019; Stensletten et al, 2014), such as family members, relatives and friends (Wawrziczny et al, 2017). Lin et al (2019) found that caregivers had increased burden to take care of activities of daily living and neuropsychiatric symptoms of people with dementia and caregivers also suffered from moderate emotional distress (Caceres et al, 2016; Otero et al, 2019), depression and anxiety (Qiu et al, 2019), grief (Li et al, 2019; Sanders et al, 2007), stress (Correa et al, 2019; Podgorski, 2018), burden (Allen et al, 2017; Yu et al, 2018) and affiliate stigma (Chang et al, 2016; Saffari et al, 2019; Su & Chang, 2020). These negative emotional reactions ultimately result in negative effects on family caregivers' health, both physically and mentally (Meichsner et al, 2017).…”