C
Cindy Brach
Researcher at Agency for Healthcare Research and Quality
Publications - 60
Citations - 6157
Cindy Brach is an academic researcher from Agency for Healthcare Research and Quality. The author has contributed to research in topics: Health care & Health literacy. The author has an hindex of 28, co-authored 60 publications receiving 5240 citations. Previous affiliations of Cindy Brach include United States Department of Health and Human Services & Anschutz Medical Campus.
Papers
More filters
Journal ArticleDOI
Evidence On The Chronic Care Model In The New Millennium
TL;DR: Accumulated evidence appears to support the Chronic Care Model as an integrated framework to guide practice redesign, and studies suggest that redesigning care using the CCM leads to improved patient care and better health outcomes.
Journal ArticleDOI
Can Cultural Competency Reduce Racial and Ethnic Health Disparities? A Review and Conceptual Model:
Cindy Brach,Irene Fraser +1 more
TL;DR: A conceptual model of cultural competency’s potential to reduce racial and ethnic health disparities is developed, using the cultural Competency and disparities literature to lay the foundation for the model and inform assessments of its validity.
Journal ArticleDOI
Development of the Patient Education Materials Assessment Tool (PEMAT): A new measure of understandability and actionability for print and audiovisual patient information
TL;DR: The PEMAT demonstrated strong internal consistency, reliability, and evidence of construct validity with consumers and readability assessments and can help professionals judge the quality of materials.
Journal ArticleDOI
Ten Attributes of Health Literate Health Care Organizations
Journal ArticleDOI
A Proposed ‘Health Literate Care Model’ Would Constitute A Systems Approach To Improving Patients’ Engagement In Care
TL;DR: A Health Literate Care Model is proposed that would weave health literacy strategies into the widely adopted Care Model (formerly known as the Chronic Care Model) and calls for first approaching all patients with the assumption that they are at risk of not understanding their health conditions or how to deal with them, and subsequently confirming and ensuring patients' understanding.