Open AccessPatient engagement with research: European population register study
Author(s) -
McKevitt Christopher,
Fudge Nina,
Crichton Siobhan,
Bejot Yannick,
Daubail Benoît,
Di Carlo Antonio,
Fearon Patricia,
KolominskyRabas Peter,
Sheldenkar Anita,
Newbound Sophie,
Wolfe Charles DA
Publication year - 2015
Publication title -
health expectations
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.314
H-Index - 74
eISSN - 1369-7625
pISSN - 1369-6513
DOI - 10.1111/hex.12315
Subject(s) - register (sociolinguistics) , stroke (engine) , medicine , family medicine , population , health care , psychology , nursing , environmental health , mechanical engineering , philosophy , linguistics , engineering , economics , economic growth
Abstract Background Lay involvement in implementation of research evidence into practice may include using research findings to guide individual care, as well as involvement in research processes and policy development. Little is known about the conditions required for such involvement. Aim To assess stroke survivors’ research awareness, use of research evidence in their own care and readiness to be involved in research processes. Methods Cross sectional survey of stroke survivors participating in population‐based stroke registers in six European centres. Results The response rate was 74% (481/647). Reasons for participation in register research included responding to clinician request (56%) and to ‘give something back’ (19%); however, 20% were unaware that they were participating in a stroke register. Research awareness was generally low: 57% did not know the purpose of the register they had been recruited to; 73% reported not having received results from the register they took part in; 60% did not know about any research on stroke care. Few participants (7.6%) used research evidence during their consultations with a doctor. The 34% of participants who were interested in being involved in research were younger, more highly educated and already research aware. Conclusions Across Europe, stroke survivors already participating in research appear ill informed about stroke research. Researchers, healthcare professionals and patient associations need to improve how research results are communicated to patient populations and research participants, and to raise awareness of the relationship between research evidence and increased quality of care.