“…Written and verbal consent was collected from people with dementia and partners and all data were kept confidential (World Medical Association, 2013). Despite the information of voluntary participation, underlying power structure within the relationship may influence choice (Braybrook, Mróz, Robertson, White, & Milnes, 2017). It is, therefore, important that the researcher is responsive and applies a “process consent” method (Hellström, Nolan, Nordenfeldt, & Lundh, 2007), whereby the researcher enables participants to make informed decision from the point of initial contact to completion of the study (Dewing, 2008).…”