Patient and healthcare professional eHealth literacy and needs for systemic sclerosis support: a mixed methods study

Author:

Kocher AgnesORCID,Simon Michael,Dwyer Andrew A,Blatter Catherine,Bogdanovic Jasmina,Künzler-Heule Patrizia,Villiger Peter M,Dan Diana,Distler Oliver,Walker Ulrich AORCID,Nicca Dunja

Abstract

ObjectivesWe engaged patients with systemic sclerosis (SSc) and healthcare professionals to assess electronic health (eHealth) literacy and needs relating to web-based support using internet-based information and communication technologies (ICT).MethodsWe employed an explanatory sequential mixed methods design. First, we conducted a cross-sectional survey in patients (n=101) and professionals (n=47). Next, we conducted three focus groups with patients, family members and professionals (n=17).ResultsOf patients, 89.1% used ICT at least weekly for private communication. Patients reported relatively high comprehension of eHealth information (x¯ =6.7, 95% CI: 6.2 to 7.3, range 1–10), yet were less confident evaluating information reliability (x¯ =5.8, 95% CI: 5.1 to 6.4) and finding eHealth apps (x¯ =4.8, 95% CI: 4.2 to 5.4). Patients and professionals reported little experience with web-based self-management support. Focus groups revealed ‘considering non-ICT-accessible groups and ‘fitting patients’ and professionals’ technology as crucial for acceptability. In relation to understanding/appraising eHealth, participants highlighted that general SSc information is not tailored to individual’s disease course. Recommendations included ‘providing timely, understandable and safe information and ‘empowering end-users in ICT and health decision-making skills. Professionals expressed concerns about lacking resources. Patients were concerned about data security and person-centredness. Key eHealth drivers included ‘addressing end-user perceptions and ‘putting people at the centre of technology.ConclusionsPatients and professionals need education/training to support uptake of eHealth resources. Key elements include guiding patients to timely/reliable information and using eHealth to optimise patient–provider communication. Design that is responsive to end-users’ needs and considers individuals with limited eHealth literacy and/or ICT access appears to be critical for acceptability.

Funder

Swiss League Against Rheumatism

Swiss Nursing Science Foundation

Publisher

BMJ

Subject

Immunology,Immunology and Allergy,Rheumatology

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