This paper is in the following e-collection/theme issue:

Design and Usability of Clinical Software and EHRs (268) Personal Health Records, Patient-Accessible Electronic Health Records, Patient Portals (573) Focus Groups and Qualitative Research for Human Factors Research (851) Consumer & Patient Education and Shared-Decision Making (679) Caregiving and Parenting for Chronic Pediatric Diseases (82) Chronic Conditions (270)

Published on in Vol 11 (2024)

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/48359, first published .
Toward Personalized Care and Patient Empowerment and Perspectives on a Personal Health Record in Hemophilia Care: Qualitative Interview Study

Toward Personalized Care and Patient Empowerment and Perspectives on a Personal Health Record in Hemophilia Care: Qualitative Interview Study

Toward Personalized Care and Patient Empowerment and Perspectives on a Personal Health Record in Hemophilia Care: Qualitative Interview Study

Authors of this article:

Martijn R Brands1, 2 Author Orcid Image ;   Lotte Haverman2, 3 Author Orcid Image ;   Jelmer J Muis2, 3 Author Orcid Image ;   Mariëtte H E Driessens4 Author Orcid Image ;   Stephan Meijer4 Author Orcid Image ;   Felix J M van der Meer5, 6 Author Orcid Image ;   Marianne de Jong7 Author Orcid Image ;   Johanna G van der Bom8 Author Orcid Image ;   Marjon H Cnossen9 Author Orcid Image ;   Karin Fijnvandraat1, 2, 10 Author Orcid Image ;   Samantha C Gouw1, 2, 8 Author Orcid Image
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