Literature DB >> 30362905

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

Karen M Barclay-Moss1, Natasha A Lannin2,3, Brenda Grabsch1, Monique Kilkenny1,4, Dominique A Cadilhac1,4.   

Abstract

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.

Entities:  

Keywords:  Follow-up; clinical registry; quality improvement; stroke; survey methods

Mesh:

Year:  2018        PMID: 30362905     DOI: 10.1177/1747493018806190

Source DB:  PubMed          Journal:  Int J Stroke        ISSN: 1747-4930            Impact factor:   5.266


  1 in total

1.  Patient-reported outcome measures (PROMs) use in post-stroke patient care and clinical practice: a realist synthesis protocol.

Authors:  A Smith; J Hewitt; T J Quinn; M Robling
Journal:  Syst Rev       Date:  2021-04-28
  1 in total

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