“…Although several studies have been conducted on stroke caregivers’ QOL, anxiety, depression and burden, only a few of them have been longitudinal, examining these variables during the first year from when the survivor is discharged home after the stroke and the caregiver starts to experience caregiving (Chuluunbaatar, Chou, & Pu, ; Godwin et al., ; Jonsson, Lindgren, Hallstrom, Norrving, & Lindgren, ; Kruithof et al., ; Nir, Greenberger, & Bachner, ). Also, only few studies (Han et al., ; Kruithof et al., ; Malhotra et al., ; Pucciarelli et al., ) have identified with a longitudinal design predictors of stroke caregivers’ QOL, anxiety, depression and burden. The first year after a stroke has been shown to be the most challenging for both stroke survivors and their caregivers (Chuluunbaatar et al., ; Jonsson et al., ) because, during this year, stroke survivors struggle with their disabilities (de Weerd, Rutgers, Groenier, & van der Meer, ) and caregivers must assume a new role in their lives (Simeone et al., ).…”