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Dive into the research topics where Alison Rein is active.

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Featured researches published by Alison Rein.


Journal of Comparative Effectiveness Research | 2015

Evaluating patient and stakeholder engagement in research: moving from theory to practice

Laura Esmail; Emily Moore; Alison Rein

Despite the growing demand for research that engages stakeholders, there is limited evidence in the literature to demonstrate its value - or return on investment. This gap indicates a general lack of evaluation of engagement activities. To adequately inform engagement activities, we need to further investigate the dividends of engaged research, and how to evaluate these effects. This paper synthesizes the literature on hypothesized impacts of engagement, shares what has been evaluated and identifies steps needed to reduce the gap between engagements promises and the underlying evidence supporting its practice. This assessment provides explicit guidance for better alignment of engagements promised benefits with evaluation efforts and identifies specific areas for development of evaluative measures and better reporting processes.


Journal of Medical Internet Research | 2013

Considerations for community-based mHealth initiatives: insights from three Beacon Communities.

Nebeyou Abebe; Korey L Capozza; Terrisca R Des Jardins; David Kulick; Alison Rein; Abigail Schachter; Scott Turske

Mobile health (mHealth) is gaining widespread attention for its potential to engage patients in their health and health care in their daily lives. Emerging evidence suggests that mHealth interventions can be used effectively to support behavior change, but numerous challenges remain when implementing these programs at the community level. This paper provides an overview of considerations when implementing community-based mHealth initiatives, based on the experiences of three Beacon Communities across the United States that have launched text messaging (short message service, SMS) pilot programs aimed at diabetes risk reduction and disease management. The paper addresses lessons learned and suggests strategies to overcome challenges related to developing text message content, conducting marketing and outreach, enrolling participants, engaging providers, evaluating program effectiveness, and sustaining and scaling the programs.


eGEMs (Generating Evidence & Methods to improve patient outcomes) | 2014

Learning from Health Information Exchange Technical Architecture and Implementation in Seven Beacon Communities

Douglas McCarthy; Karen Propp; Alexander (Sandy) Cohen; Raj Sabharwal; Abigail Schachter; Alison Rein

As health care providers adopt and make “meaningful use” of health information technology (health IT), communities and delivery systems must set up the infrastructure to facilitate health information exchange (HIE) between providers and numerous other stakeholders who have a role in supporting health and care. By facilitating better communication and coordination between providers, HIE has the potential to improve clinical decision-making and continuity of care, while reducing unnecessary use of services. When implemented as part of a broader strategy for health care delivery system and payment reform, HIE capability also can enable the use of analytic tools needed for population health management, patient engagement in care, and continuous learning and improvement. The diverse experiences of seven communities that participated in the three-year federal Beacon Community Program offer practical insight into factors influencing the technical architecture of exchange infrastructure and its role in supporting improved care, reduced cost, and a healthier population. The case studies also document challenges faced by the communities, such as significant time and resources required to harmonize variations in the interpretation of data standards. Findings indicate that their progress developing community-based HIE strategies, while driven by local needs and objectives, is also influenced by broader legal, policy, and market conditions.


eGEMs (Generating Evidence & Methods to improve patient outcomes) | 2014

Data Governance and Data Sharing Agreements for Community-Wide Health Information Exchange: Lessons from the Beacon Communities

Claudia Allen; Terrisca R Des Jardins; Arvela R. Heider; Kristin A. Lyman; Lee McWilliams; Alison Rein; Abigail Schachter; Ranjit Singh; Barbara Sorondo; Joan Topper; Scott Turske

Purpose: Unprecedented efforts are underway across the United States to electronically capture and exchange health information to improve health care and population health, and reduce costs. This increased collection and sharing of electronic patient data raises several governance issues, including privacy, security, liability, and market competition. Those engaged in such efforts have had to develop data sharing agreements (DSAs) among entities involved in information exchange, many of whom are “nontraditional” health care entities and/or new partners. This paper shares lessons learned based on the experiences of six federally funded communities participating in the Beacon Community Cooperative Agreement Program, and offers guidance for navigating data governance issues and developing DSAs to facilitate community-wide health information exchange. Innovation: While all entities involved in electronic data sharing must address governance issues and create DSAs accordingly, until recently little formal guidance existed for doing so – particularly for community-based initiatives. Despite this lack of guidance, together the Beacon Communities’ experiences highlight promising strategies for navigating complex governance issues, which may be useful to other entities or communities initiating information exchange efforts to support delivery system transformation. Credibility: For the past three years, AcademyHealth has provided technical assistance to most of the 17 Beacon Communities, 6 of whom contributed to this collaborative writing effort. Though these communities varied widely in terms of their demographics, resources, and Beacon-driven priorities, common themes emerged as they described their approaches to data governance and DSA development. Conclusions: The 6 Beacon Communities confirmed that DSAs are necessary to satisfy legal and market-based concerns, and they identified several specific issues, many of which have been noted by others involved in network data sharing initiatives. More importantly, these communities identified several promising approaches to timely and effective DSA development, including: stakeholder engagement; identification and effective communication of value; adoption of a parsimonious approach; attention to market-based concerns; flexibility in adapting and expanding existing agreements and partnerships; and anticipation of required time and investment.


Journal of Health Care for the Poor and Underserved | 2015

Patient Engagement and Activation in Three Underserved Beacon Communities

Terrisca R Des Jardins; Shenetta A. Drone; Susan Hashisaka; Jobyna Hazzard; Susan B. Hunt; Kimberly Massey; Alison Rein; Abigail Schachter; Scott Turske

Whether the setting is urban, rural, or somewhere in between, engagement strategies for the underserved require a great deal of flexibility and sensitivity to the socioeconomic, cultural, and geographic conditions of the patient population. The following report details how three unique communities designed specific strategies to engage underserved populations in the management of their chronic conditions.


Journal of Health Care for the Poor and Underserved | 2016

Leveraging Health IT to Reduce Disparities in Three Underserved Beacon Communities.

Terrisca R Des Jardins; Shenetta A. Drone; Susan Hashisaka; Jobyna Hazzard; Susan B. Hunt; Kimberly Massey; Alison Rein; Abigail Schachter; Scott Turske

Using health information technology (IT) can potentially address health disparities by increasing access to care, delivering higher-quality care, improving patient-provider communication, and enhancing patient safety. It describes challenges encountered by three underserved Beacon Communities that implemented health IT interventions, including inadequate connectivity infrastructure, technical support, expertise, and financial resources; provider shortages and staff turnover; and equipment theft.


Journal of General Internal Medicine | 2016

Patient and Stakeholder Engagement in the PCORI Pilot Projects: Description and Lessons Learned

Laura P. Forsythe; Lauren E. Ellis; Lauren Edmundson; Raj Sabharwal; Alison Rein; Kristen Konopka; Lori Frank


Medical Care | 2012

The Electronic Data Methods (EDM) forum for comparative effectiveness research (CER).

Erin Holve; Courtney Segal; Marianne Hamilton Lopez; Alison Rein; Beth Johnson


Archive | 2012

Approaches to Using Protected Health Information (PHI) for Patient-Centered Outcomes Research (PCOR): Regulatory Requirements, De-identification Strategies, and Policy

Raj Sabharwal; Erin Holve; Alison Rein; Courtney Segal


Journal of Comparative Effectiveness Research | 2017

Attitudes toward comparative effectiveness research and patient engagement among reproductive health clinicians

Julia E. Kohn; Zoe Unger; Jennifer Dolatshahi; Hannah R. Simons; Alison Rein

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Joan Topper

Geisinger Health System

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Kristen Konopka

Patient-Centered Outcomes Research Institute

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