Stroke survivors and their caregivers often experience substantial challenges across the journey from symptom onset to discharge preparation. Understanding their evolving needs and care experiences may help improve patient-centered support and care across different stages of the stroke journey. This study aimed to explore the experiences and needs of patients with stroke and their caregivers across this in-hospital care journey. A longitudinal qualitative descriptive study was conducted using semi-structured interviews with hospitalized stroke patients and their primary family caregivers. Each patient-caregiver dyad was interviewed jointly at two time points during hospitalization: the acute phase (within 48 h of admission) and the discharge preparation phase (within 24 h before discharge). All interviews were audio-recorded, transcribed verbatim, and analyzed using conventional content analysis; the categories were subsequently organized within a patient journey framework. Fourteen patient–caregiver dyads were included. Conventional content analysis identified 28 subcategories, which were organized into a patient journey map from symptom onset to discharge preparation. The map captured stage-specific needs, pain points, and emotional experiences, showing a shift from urgent diagnosis and treatment concerns to recovery, rehabilitation, and discharge-related support needs. The needs, pain points, and emotional experiences of patients with stroke and their caregivers evolved across different stages of the stroke care journey. Continuous, stage-specific, and patient-centered support may help address unmet needs and improve care experiences during transitions from acute treatment to recovery and discharge.
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Rong et al. (2026) studied this question.
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