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Recruiting
NCT05646589
A Person-centred Care Transition Support for People With Stroke/TIA
Conditions: Stroke, Transient Ischemic Attack
Sex: All
Ages: 18 Years – N/A
Phase: NA
Enrollment: 336
Sponsor: Karolinska Institutet
Location: Sweden
Summary
The goal of this clinical trial is to test a person-centred care transition support in people with stroke/TIA.
The main questions it aims to answer are:Does a multi-component care transition intervention have an effect on perceived quality of care transitions, health literacy, collected medications, medication adherence, perceived person-centeredness, functioning, recurrent stroke/TIA, healthcare utilization and caregiver burden?What are the experiences of the intervention components and the implementation process?How does the intervention get adapted and implemented in practice?What contextual moderators and mechanisms of the intervention can likely explain the potential effects of the intervention?Participants will receive a person-centred care transition support that includes a set of activities targeting how healthcare professionals can improve quality with care transition and support health literacy for self-management of secondary stroke prevention for persons who are to be discharged from hospitals after stroke or TIA.Researchers will compare participants who receive the person-centred care transition support with participants receiving regular care transitions to see if the person-centred care transition support has any effects on perceived quality of care transitions, health literacy, collected medications, medication adherence, perceived person-centeredness, functioning, recurrent stroke/TIA, healthcare utilization and caregiver burden.
Eligibility Criteria
Inclusion Criteria:patients who have had a first time ever or recurrent stroke or TIA; who are to be discharged from the participating hospitals to home and referred to a neurorehabilitation team for continued rehabilitation; and who are able to give informed consent by themselves.Exclusion Criteria:unable to give informed consent, due to e.g., severe aphasia or dementia.
Source: ClinicalTrials.gov (NCT05646589). StuddyBuddy aggregates publicly available trial information.