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Preferences of the public for sharing health data:Discrete choice experiment

Authors :
Johansson, Jennifer Viberg
Bentzen, Heidi Beate
Shah, Nisha
Haraldsdóttir, Eik
Jónsdóttir, Gu björg Andrea
Kaye, Jane
Mascalzoni, Deborah
Veldwijk, Jorien
Johansson, Jennifer Viberg
Bentzen, Heidi Beate
Shah, Nisha
Haraldsdóttir, Eik
Jónsdóttir, Gu björg Andrea
Kaye, Jane
Mascalzoni, Deborah
Veldwijk, Jorien
Source :
Johansson , J V , Bentzen , H B , Shah , N , Haraldsdóttir , E , Jónsdóttir , G B A , Kaye , J , Mascalzoni , D & Veldwijk , J 2021 , ' Preferences of the public for sharing health data : Discrete choice experiment ' , JMIR Medical Informatics , vol. 9 , no. 7 , e29614 .
Publication Year :
2021

Abstract

Background: Digital technological development in the last 20 years has led to significant growth in digital collection, use, and sharing of health data. To maintain public trust in the digital society and to enable acceptable policy-making in the future, it is important to investigate people's preferences for sharing digital health data. Objective: The aim of this study is to elicit the preferences of the public in different Northern European countries (the United Kingdom, Norway, Iceland, and Sweden) for sharing health information in different contexts. Methods: Respondents in this discrete choice experiment completed several choice tasks, in which they were asked if data sharing in the described hypothetical situation was acceptable to them. Latent class logistic regression models were used to determine attribute-level estimates and heterogeneity in preferences. We calculated the relative importance of the attributes and the predicted acceptability for different contexts in which the data were shared from the estimates. Results: In the final analysis, we used 37.83% (1967/5199) questionnaires. All attributes influenced the respondents' willingness to share health information (P<.001). The most important attribute was whether the respondents were informed about their data being shared. The possibility of opting out from sharing data was preferred over the opportunity to consent (opt-in). Four classes were identified in the latent class model, and the average probabilities of belonging were 27% for class 1, 32% for class 2, 23% for class 3, and 18% for class 4. The uptake probability varied between 14% and 85%, depending on the least to most preferred combination of levels. Conclusions: Respondents from different countries have different preferences for sharing their health data regarding the value of a review process and the reason for their new use. Offering respondents information about the use of their data and the possibility to opt out is the most prefer

Details

Database :
OAIster
Journal :
Johansson , J V , Bentzen , H B , Shah , N , Haraldsdóttir , E , Jónsdóttir , G B A , Kaye , J , Mascalzoni , D & Veldwijk , J 2021 , ' Preferences of the public for sharing health data : Discrete choice experiment ' , JMIR Medical Informatics , vol. 9 , no. 7 , e29614 .
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1313637822
Document Type :
Electronic Resource