“…Most data sources (n = 73/89, 82%) conducted co-design with multiple participant types (e.g., individuals with stroke, stroke family members/caregivers, stroke clinicians). Of the included data sources, nearly all (n = 87/89, 98%) involved people with stroke, and some specifically targeted individuals with aphasia (e.g., [ 43 , 46 , 57 , 65 , 67 , 92 , 94 ]), with a loss of visual field (e.g., [ 70 ]), current or former hospital inpatients (e.g., [ 32 , 45 , 49 , 50 , 66 , 79 , 86 , 87 ]), with cognitive and/or physical impairments (e.g., [ 85 ]), with certain levels of physical or functional impairments (e.g., “severe upper-limb deficits” [ 91 ] and “mild to moderate level of disability” [ 55 ]), First Nations community members with stroke [ 64 ] and Aboriginal and/or Torres Strait Islander Peoples with stroke [ 43 ]. A few researchers specified that cognitive ability was determined through clinical judgement and/or based on whether an individual could provide informed consent and participate in the study activities [ 74 , 104 ].…”