Using Health Information Technology to Engage Communities in Health, Education, and Research

Marriott, Lisa K.; Nelson, David A.; Allen, Shauntice; Calhoun, Karen; Eldredge, Christina; Kimminau, Kim S.; Lucero, Robert; Pineda-Reyes, Fernando; Rumala, Bernice B.; Varanasi, Arti; Wasser, June S.; Shannon, Jackilen

doi:10.1126/scitranslmed.3003363

Cited by 8 publications

(10 citation statements)

References 14 publications

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“…Reay (2013) recommends technological solutions to improve the application of data that include evidence-based practices, an electronic clinical record system, and a MFS for continuous quality improvement. The U.S. government is driving funding efforts for the mental health care community to integrate electronic health records and 'meaningful use' metrics into their administrative systems as part of the Affordable Care Act (Marriott et al 2012). MFSs are a vital part of the current national emphasis on transforming health care by increasing the use of information technology to support clinical decision-making (DeLeon and Pachter 2010; Institute of Medicine 2001).…”

Section: The 'Golden Thread' Of Data-informed Decisionmakingmentioning

confidence: 99%

Implementing for Sustainability: Promoting Use of a Measurement Feedback System for Innovation and Quality Improvement

Douglas

Button

Casey

2014

Adm Policy Ment Health

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Measurement feedback systems (MFSs) are increasingly recognized as evidence-based treatments for improving mental health outcomes, in addition to being a useful administrative tool for service planning and reporting. Promising research findings have driven practice administrators and policymakers to emphasize the incorporation of outcomes monitoring into electronic health systems. To promote MFS integrity and protect against potentially negative outcomes, it is vital that adoption and implementation be guided by scientifically rigorous yet practical principles. In this point of view, the authors discuss and provide examples of three user-centered and theory-based principles: emphasizing integration with clinical values and workflow, promoting administrative leadership with the 'golden thread' of data-informed decision-making, and facilitating sustainability by encouraging innovation. In our experience, enacting these principles serves to promote sustainable implementation of MFSs in the community while also allowing innovation to occur, which can inform improvements to guide future MFS research.

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Section: The 'Golden Thread' Of Data-informed Decisionmakingmentioning

confidence: 99%

Implementing for Sustainability: Promoting Use of a Measurement Feedback System for Innovation and Quality Improvement

Douglas

Button

Casey

2014

Adm Policy Ment Health

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“…Literature about the application of social media in healthcare highlights the significance of these technologies in creating new opportunities for interactions and conversations between people who are involved in healthcare activities [56]. In particular, the literature points to the promising potential of social media in chronic care management, as well as the ways these technologies may challenges the process [52].…”

Section: Literature Reviewmentioning

confidence: 99%

“…Features such as making decisions about different aspects of treatments [15], negotiating work place related issue [45], educating friends and families [56], and taking part in social activities [33], are just a few to name.…”

Section: Viewing Our Findings Through the Lens Of Sociomaterialitymentioning

confidence: 99%

Exploring the Role of Social Media in Chronic Care Management

Pousti

Urquhart

Linger

2014

IFIP Advances in Information and Communication Technology

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Abstract. This paper examines how social media can support communities of patients with chronic illness and their care givers. This study is a qualitative case study and is informed by grounded theory. Sociomateriality is adopted as a theoretical lens to understand and explain the key findings. Our findings suggest that there is a dynamic relation between the contrary roles that social media in chronic care management and this is not only attributed to the functionalities of these technologies but to the attributes of patients and their states of health. We were also able to observe how these technologies are bounded up with human activities in the ways that separating them is not possible. What we learnt from our findings is that the ways patients and carers use of social media can change their perceptions about their conditions, and influence how they understand and approach the management process.

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“…In pursuing these agendas, the relationship between web technologies and CBPR should not be thought of as a one-way street. To ensure maximal community involvement, CBPR should be used as a means of supporting iterative user-centered design (Marriott et al, 2012) of new internet-based tools for the BD community (Henderson et al, 2013).…”

Section: Opportunitiesmentioning

confidence: 99%

Towards a Better Future for Canadians with Bipolar Disorder: Principles and Implementation of a Community-Based Participatory Research Model

Michalak¹,

Lane²,

Hole³

et al. 2015

ESJ

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The Collaborative RESearch Team to study psychosocial factors in bipolar disorder (CREST.BD) is a multidisciplinary network dedicated to advancing science and practice around psychosocial issues associated with bipolar disorder (BD), improving the care and wellness of people living with bipolar disorder, and strengthening services and supports for these individuals. CREST.BD specializes in community-based participatory research, in which research is conducted as a partnership between researchers and community members. This article describes the evolution of the CREST.BD network and CREST.BD's commitment to community-based participatory research in bipolar disorder research. Examples of CREST.BD projects using community-based participatory research to study stigma, quality of life, psychosocial interventions, and creativity in bipolar disorder are highlighted, and opportunities and challenges of engaging in communitybased participatory research in bipolar disorder specifically and the mental health field more broadly are discussed. This article demonstrates how CBPR can be used to enhance the relevance of research practices and products through community engagement, and how community-based participatory research can enrich knowledge exchange and mobilization.

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Using Health Information Technology to Engage Communities in Health, Education, and Research

Cited by 8 publications

References 14 publications

Implementing for Sustainability: Promoting Use of a Measurement Feedback System for Innovation and Quality Improvement

Implementing for Sustainability: Promoting Use of a Measurement Feedback System for Innovation and Quality Improvement

Exploring the Role of Social Media in Chronic Care Management

Towards a Better Future for Canadians with Bipolar Disorder: Principles and Implementation of a Community-Based Participatory Research Model

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