Research Involvement and Engagement (Jun 2021)

How to foster successful implementation of a patient reported experience measurement in the disability sector: an example of developing strategies in co-creation

  • Marjolein van Rooijen,
  • Anneke van Dijk-de Vries,
  • Stephanie Lenzen,
  • Ruth Dalemans,
  • Albine Moser,
  • Anna Beurskens

DOI
https://doi.org/10.1186/s40900-021-00287-w
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 12

Abstract

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Plain English summary Exploring care-users experiences is important for decisions to improve quality of care. This applies to care-users in the disability care in particular, as these care-users are highly dependent on their care professional. Instruments that facilitate a dialogue between care-users and care professionals about experiences with care are not always used correctly. Furthermore, it is difficult to translate outcomes into decisions about improving quality of care for the individual care-user and the organisation. In our study, care-users, care professionals, management and researchers developed strategies together to improve the use of care-user experience measures. This study aims to show the impact of all participants, including care-users, professionals, management and researchers, on developing implementation strategies. Additionally, the study aims to show how care-users can participate in developing strategies whilst having problems with communication due to intellectual, developmental and acquired disabilities. We found that care-users gave crucial input to the look and feel, and understandability and relevance of the strategies. The contribution of the professionals had impact on how to use strategies and terminology used in instructions and visuals. Management shared lessons learned and represented the needs on the policy level. Researchers used their analytical skills and facilitated the group process. Care-users were able to collaborate by taking into account their needs and because information was presented to them clearly and attractively.

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