<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Charalambous, Marina</dc:creator>
  <dc:creator>Kambanaros, Maria</dc:creator>
  <dc:creator>Annoni, Jean-Marie</dc:creator>
  <dc:date>2020-09-29</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Background: Quality of Life (QoL) questionnaires are used to describe the impact of  aphasia on stroke survivors’ life. People with aphasia (PWA) are traditionally excluded  from research, potentially leading to a mismatch between the factors chosen in the  tools and the realistic needs of PWA. The purpose of this review was to determine the  direct involvement of PWA in the creation of QoL and aphasia impact-related  questionnaires (AIR-Qs). Methods: A scoping review methodology was conducted by  an expert librarian and two independent reviewers on health sciences based on the  Preferred Reporting Items for Systematic Reviews and Metanalyses extension for  Scoping Reviews (PRISMA-ScR) protocol, through a literature search in five  databases: Medline Complete, PubMed, PsychINFO, Scopus, and Google Scholar.  Search terms included ‘stroke’, ‘people with aphasia’, ‘communication’, ‘well-being’,  and ‘quality of life’. Results: Of 952 results, 20 studies met the eligibility criteria. Of  these, only four AIR-Qs studies (20%) were found reporting the direct involvement of  PWA, while no QoL tools did so. Evidence showed involvement in the creation phase  of AIR-Q, mainly in a consultation role. Conclusions: There is an absence of a  framework for conducting and reporting the involvement of PWA in qualitative  participatory research studies, which limits effectiveness to promote equitable best  practice in aphasia rehabilitation.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/309006</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/309006/files/ann_apa.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/brainsci10100688</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Brain Sciences. - 2020, vol. 10, no. 10, p. 688</dc:source>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Are people with aphasia (pwa) involved in the creation of quality of life and aphasia impact-related questionnaires? A scoping review</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
