TY - JOUR
T1 - Development of an mHealth platform for HIV care
T2 - Gathering user perspectives through co-design workshops and interviews
AU - EmERGE Consortium
AU - Marent, Benjamin
AU - Henwood, Flis
AU - Darking, Mary
AU - Leon, Agathe
AU - West, Brian
AU - Lockhart, Daniel
AU - Garcia, David
AU - Fatz, Duncan
AU - Wallitt, Ed
AU - Beck, Eduard
AU - Gomez, Enrique
AU - Teofilo, Eugenio
AU - Gonzalez, Eva
AU - Garcia, Felipe
AU - Rodrigues, Goncalo
AU - Whetham, Jennifer
AU - Begovac, Josip
AU - Block, Koen
AU - Pereira, Letitia
AU - Apers, Ludwig
AU - Borges, Margarida
AU - Chausa, Paloma
AU - Zekan, Sime
AU - Bremner, Steven
AU - Hoornaert, Steven
AU - Mandalia, Sundhiya
N1 - Funding Information: The co-design process presented in this paper is part of the Evaluating mHealth Technology in HIV to Improve Empowerment and Health Care Utilization: Research and Innovation to Generate Evidence for Personalized Care (EmERGE) project (please refer to [20]), which is funded under the EU’s Horizon 2020 Programme (project period: 2015-2020). The project aims to develop, implement, and evaluate an mHealth platform to support self-management among HIV patients in 5 clinical sites (Brighton, Antwerp, Zagreb, Barcelona, and Lisbon). The platform is currently being integrated into clinical HIV pathways and provides users (PLWH and clinicians) with smartphone and Web apps to facilitate access to personal health data and improve patient-provider communication. Through these functionalities, the EmERGE mHealth platform aims to reduce some routine clinic visits of HIV patients and support patients to better self-manage their own care. According to international guidelines, PLWH are currently seen every 3 to 6 months [21]. However, the EmERGE mHeaIth care pathway requires HIV patients to see their consultant face-to-face only every 12 months, while they can continuously monitor their blood results and maintain contact with their clinic through the smartphone app. Previous studies that have investigated the potential of mHealth in HIV care have suggested that such reductions in hospital visits are desirable for increasing the quality of life of PLWH [18]. The EmERGE project, as a whole, aims to validate the acceptability, usability, and effectiveness of the mHealth platform; assess its impact on patient self‐management and empowerment; analyze its cost-effectiveness; and disseminate the mHealth platform across various European health care settings as a sustainable, effective, safe, and economic modality for HIV care. The co-design process, outlined in this paper, constitutes an essential part of the sociotechnical evaluation work package, which seeks to identify and support factors that can help facilitate the successful introduction of the new care pathway. In the first year of the project (June 2015 to June 2016), in the platform’s initial design phase, we undertook a co-design process among potential users of the EmERGE platform—PLWH and clinicians. The results from this process are presented in this paper and have informed the technology development. Further research is currently being carried out, as the platform is implemented, to investigate how it reconfigures practices of HIV care [22]. Study approval was obtained from the ethics committee of the University of Brighton, the National Health Service (NHS) Health Research Authority, and governance boards at each clinical site. Funding Information: EmERGE is a project funded by the EU’s Horizon 2020 Research and Innovation Programme under grant agreement no. 643736. The dissemination activities within the EmERGE project do not represent the opinion of the European community and only reflect the opinion of the authors. The scientific members of the EmERGE Consortium are Agathe Leon, BM, Brian West, Daniel Lockhart, David Garcia, Duncan Fatz, Ed Wallitt, Eduard Beck, Enrique Gomez, Eugenio Teofilo, Eva Gonzalez, Felipe Garcia, FH, Goncalo Rodrigues, Jennifer Whetham, Josip Begovac, Koen Block, Letitia Pereira, Ludwig Apers, Margarida Borges, MD, Paloma Chausa, Sime Zekan, Steven Bremner, Steven Hoornaert, and Sundhiya Mandalia. The scientific advisors are Alec Miners, Cesar Caceres, and Richard Harding. The authors would like to thank Brian West and Koen Block from EATG for providing them with valuable insights to design this study and their local partners (Terrence Higgins Trust, United Kingdom; Sensoa, Belgium; Lux Vitae, Croatia; Projecte dels NOMS, Spain; and GAT, Portugal) for supporting them in the recruitment of study participants and in facilitating co-design workshops with PLWH. The authors would like to thank the lead clinicians at each study site Dr Jennifer Whetham, Dr Ludwig Apers, Dr Josip Begovac, Dr Agathe Leon, Dr Eugénio Teófilo, and Dr Margarida Borges for supporting the recruitment of clinicians. Finally, the authors thank the PLWH and clinicians for their commitment and willingness to participate in this co-design research. Publisher Copyright: © Benjamin Marent, Flis Henwood, Mary Darking, EmERGE Consortium.
PY - 2018/10
Y1 - 2018/10
N2 - Background: Despite advances in testing and treatment, HIV incidence rates within European countries are at best stable or else increasing. mHealth technology has been advocated to increase quality and cost-effectiveness of health services while dealing with growing patient numbers. However, studies suggested that mHealth apps are rarely adopted and often considered to be of low quality by users. Only a few studies (conducted in the United States) have involved people living with HIV (PLWH) in the design of mHealth.Objective: The goal of this study was to facilitate a co-design process among PLWH and clinicians across 5 clinical sites in the European Union to inform the development of an mHealth platform to be integrated into clinical care pathways. We aimed to (1) elicit experiences of living with HIV and of working in HIV care, (2) identify mHealth functionalities that are considered useful for HIV care, and (3) identify potential benefits as well as concerns about mHealth.Methods: Between January and June 2016, 14 co-design workshops and 22 semistructured interviews were conducted, involving 97 PLWH and 63 clinicians. Data were analyzed thematically and iteratively, drawing on grounded theory techniques.Results: Findings were established into 3 thematic clusters: (1) approaching the mHealth platform, (2) imagining the mHealth platform, and (3) anticipating the mHealth platform’s implications. Co-design participants approached the mHealth platform with pre-existing concerns arising from their experiences of receiving or providing care. PLWH particularly addressed issues of stigma and questioned how mHealth could enable them to manage their HIV. Clinicians problematized the compatibility of mHealth with existing information technology systems and questioned which patients should be targeted by mHealth. Imagining the potential of mHealth for HIV care, co-design participants suggested medical functionalities (accessing test results, managing medicines and appointments, and digital communication channels), social functionalities (peer support network, international travel, etc), and general features (security and privacy, credibility, language, etc). Co-design participants also anticipated potential implications of mHealth for self-management and the provision of care.Conclusions: Our approach to co-design enabled us to facilitate early engagement in the mHealth platform, enabling patient and clinician feedback to become embedded in the development process at a preprototype phase. Although the technologies in question were not yet present, understanding how users approach, imagine, and anticipate technology formed an important source of knowledge and proved highly significant within the technology design and development process.
AB - Background: Despite advances in testing and treatment, HIV incidence rates within European countries are at best stable or else increasing. mHealth technology has been advocated to increase quality and cost-effectiveness of health services while dealing with growing patient numbers. However, studies suggested that mHealth apps are rarely adopted and often considered to be of low quality by users. Only a few studies (conducted in the United States) have involved people living with HIV (PLWH) in the design of mHealth.Objective: The goal of this study was to facilitate a co-design process among PLWH and clinicians across 5 clinical sites in the European Union to inform the development of an mHealth platform to be integrated into clinical care pathways. We aimed to (1) elicit experiences of living with HIV and of working in HIV care, (2) identify mHealth functionalities that are considered useful for HIV care, and (3) identify potential benefits as well as concerns about mHealth.Methods: Between January and June 2016, 14 co-design workshops and 22 semistructured interviews were conducted, involving 97 PLWH and 63 clinicians. Data were analyzed thematically and iteratively, drawing on grounded theory techniques.Results: Findings were established into 3 thematic clusters: (1) approaching the mHealth platform, (2) imagining the mHealth platform, and (3) anticipating the mHealth platform’s implications. Co-design participants approached the mHealth platform with pre-existing concerns arising from their experiences of receiving or providing care. PLWH particularly addressed issues of stigma and questioned how mHealth could enable them to manage their HIV. Clinicians problematized the compatibility of mHealth with existing information technology systems and questioned which patients should be targeted by mHealth. Imagining the potential of mHealth for HIV care, co-design participants suggested medical functionalities (accessing test results, managing medicines and appointments, and digital communication channels), social functionalities (peer support network, international travel, etc), and general features (security and privacy, credibility, language, etc). Co-design participants also anticipated potential implications of mHealth for self-management and the provision of care.Conclusions: Our approach to co-design enabled us to facilitate early engagement in the mHealth platform, enabling patient and clinician feedback to become embedded in the development process at a preprototype phase. Although the technologies in question were not yet present, understanding how users approach, imagine, and anticipate technology formed an important source of knowledge and proved highly significant within the technology design and development process.
KW - Community-based participatory research
KW - HIV
KW - Health services
KW - Information technology
KW - Medical
KW - Mobile applications
KW - Patient participation
KW - Self-management
KW - Sexual health
KW - Sociology
KW - Telemedicine
KW - mHealth
UR - http://www.scopus.com/inward/record.url?scp=85053306697&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85053306697&partnerID=8YFLogxK
U2 - 10.2196/mhealth.9856
DO - 10.2196/mhealth.9856
M3 - Article
SN - 2291-5222
VL - 6
JO - JMIR mHealth and uHealth
JF - JMIR mHealth and uHealth
IS - 10
M1 - e184
ER -