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. 2022 Sep 14;17(1):357.
doi: 10.1186/s13023-022-02514-3.

Identifying project topics and requirements in a citizen science project in rare diseases: a participative study

Affiliations

Identifying project topics and requirements in a citizen science project in rare diseases: a participative study

Michaela Neff et al. Orphanet J Rare Dis. .

Abstract

Background: Due to their low prevalence (< 5 in 10,000), rare diseases are an important area of research, with the active participation of those affected being a key factor. In the Citizen Science project "SelEe" (Researching rare diseases in a citizen science approach), citizens collaborate with researchers using a digital application, developed as part of the project together with those affected, to answer research questions on rare diseases. The aim of this study was to define the rare diseases to be considered, the project topics and the initial requirements for the implementation in a digital application.

Methods: To address our research questions, we took several steps to engage citizens, especially those affected by rare diseases. This approach included the following methods: pre- and post-survey (questionnaire), two workshops with focus group discussion and a requirements analysis workshop (with user stories).

Results: In the pre-survey, citizens suggested 45 different rare diseases and many different disease groups to be considered in the project. Two main project topics (A) "Patient-guided documentation and data collection" (20 votes) and (B) "Exchange of experience and networking" (13 votes) were identified as priorities in the workshops and ranked in the post-survey. The requirements workshop resulted in ten user stories and six initial requirements to be implemented in the digital application.

Conclusion: Qualitative, citizen science research can be used to collectively identify stakeholder needs, project topics and requirements for a digital application in specific areas, such as rare diseases.

Keywords: Citizen science; Patient science; Qualitative research; Rare diseases.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Steps of the study's multi-step approach
Fig. 2
Fig. 2
Interactive word cloud—which project topics would you like to propose?
Fig. 3
Fig. 3
Results from category formation
Fig. 4
Fig. 4
Voting on topics in post-survey
Fig. 5
Fig. 5
Story cards of RD-affected persons

References

    1. COM. Council Recommendation (EU) of 8 June 2009 on an action in the field of rare diseases. 2009. Available from: https://eur-lex.europa.eu/legal-content/EN/ALL/?uri=celex:32009H0703(02). Accessed 01 June 2022.
    1. Nguengang Wakap S, Lambert DM, Olry A, Rodwell C, Gueydan C, Lanneau V, et al. Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database. Eur J Hum Genet. 2020;28:165–173. doi: 10.1038/s41431-019-0508-0. - DOI - PMC - PubMed
    1. Institute of Medicine (US) Committee on Accelerating Rare Diseases Research and Orphan Product Development; Field MJ, Boat TF, editors. Profile of Rare Diseases. Rare Dis Orphan Prod Accel Res Dev . Washington (DC): National Academies Press (US); 2010. p. 41–72. Available from: https://www.ncbi.nlm.nih.gov/books/NBK56184/. Accessed 29 Mar 2022. - PubMed
    1. Dong D, Chung RY-N, Chan RHW, Gong S, Xu RH. Why is misdiagnosis more likely among some people with rare diseases than others? Insights from a population-based cross-sectional study in China. Orphanet J Rare Dis. 2020;15:307. doi: 10.1186/s13023-020-01587-2. - DOI - PMC - PubMed
    1. Aymé S, Schmidtke J. Networking for rare diseases: a necessity for Europe. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 2007;50:1477–1483. doi: 10.1007/s00103-007-0381-9. - DOI - PubMed

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