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Stroke survivor follow-up in a national registry: Lessons learnt from respondents who completed telephone interviews.

Karen M Barclay-MossNatasha A LanninBrenda GrabschMonique F KilkennyDominique Ann-Michele Cadilhac
Published in: International journal of stroke : official journal of the International Stroke Society (2018)
The Australian Stroke Clinical Registry (AuSCR) collects patient-reported outcomes at 90-180 days post-stroke. During telephone interviews, stroke survivors or their carers/family members often explain why they did not respond to a previously mailed survey. This feedback is useful to explore respondents' experiences of the follow-up process. Three main reasons for not returning surveys included: health-related time constraints, confusion about survey questions, and stroke denial. Such information is helpful in improving procedures for clinical quality disease registries and researchers using postal questionnaires.
Keyphrases
  • atrial fibrillation
  • patient reported outcomes
  • cross sectional
  • mental health
  • young adults
  • quality improvement
  • cerebral ischemia
  • healthcare
  • social media