September 13th, 2016
Researchers face challenges in retaining underserved populations for web-based research, a recent study finds.
The findings were published online July 28 in Genetics in Medicine.
A study that provided online genetic ancestry results to participants found that low-income Americans and people who did not finish high school were less likely to log in, said Sarah Hartz, MD, PhD, lead study author and assistant professor of psychiatry at the Washington University School of Medicine in St. Louisâ€™ Department of Psychiatry.
Hartz said the results are troubling to her in light of the Precision Medicine Initiative, a national program launched under President Barack Obama in 2015 that is dedicated to recruiting a diverse group of Americans for genetic research, she said.
â€śWe have to recruit these people,â€ť Hartz told The Nationâ€™s Health. â€śIf we donâ€™t itâ€™s going to be worseâ€¦it will be very difficult to reduce disparities in the future.â€ť Learn more
August 31st, 2016
— Bill Barberg (@billbarberg) July 21, 2016
August 24th, 2016
How to Read Beyond the Headline: 9 Essential Questions to Evaluate Medical News Ben Goldacre writing in Bad Science classified science reporting as falling into three categories â€“ wacky stories, scare stories and breakthrough stories; the last of which he views as â€ťa more subtly destructive category of science storyâ€ť. Whether you get your news through digital or traditional means, you canâ€™t fail to notice the regularity with which journalists report on the latest medical breakthroughs. Some of these reports are sensationalist (â€ścoffee causes cancerâ€ť) and fairly easy to dismiss; but do you know how to separate fact from fiction when it comes to less sensationalist headlines?
July 7th, 2016
Despite striking ethnic disparities in the incidence and mortality of diseases like cancer and respiratory disease, minorities are not well represented in clinical trials. A paper out in the journal PLOS Medicine says two main barriers to achieving diverse clinical trials are the expense of recruiting minority subjects, and fears of exploitation in medical research.
June 10th, 2016
The Mayo Clinic Center for Clinical and Translational Science (CCaTS) is pleased to announce that Aaron Mangold, M.D., is the recipient of the 2016 Community Health: Assessment and Improvement Measures Program (CHAMP) award.
Dr. Mangoldâ€™s project, Improving Access to Care Through the Establishment of a Local, Tele-Dermatology Network, addresses an identified community health need, and will engage stake-holders in all phases of his research. Dr. Mangold is assistant professor of Dermatology, and senior associate consultant in Dermatology at Mayo Clinic in Scottsdale.
Through its CHAMP program, CCaTS supports research projects that address community health needs as identified by local community health needs reports such as the Olmsted County, Minnesota, Community Health Needs Assessment 2013 report or the local Mayo Clinic Hospital Community Health Needs Assessment reports.
June 9th, 2016
An estimated 43.6 million American adultsâ€”nearly one in fiveâ€”have mental illness. Anxiety and mood disorders, including depression, are the most common forms. While these conditions are usually treatable, clinicians often donâ€™t have a good way to predict who will respond to which therapies, so patients may have to try different types of treatments.
June 8th, 2016
As issues around diversity, equity, inclusion and cultural competency have risen to the forefront, many grantmakers are trying to make their processes more equitable, both in terms of dollars awarded and in who receives the money. But, from the perspective of grassroots organizations led by and serving communities of color, common foundation and nonprofit practices can feel disingenuous and even counterproductive to this goal. If grantmakers want marginalized communities to be engaged, they need to fund, trust and support them directly, believes Vu Le. This means resisting the tendency to practice â€śtrickle-down community engagement.â€ť Le will speak candidly about this and other well-intentioned but harmful behaviors in the sector. Heâ€™ll suggest ways to make funding more accessible, lift up individuals and communities of color, and demonstrate trust that communities have solutions
March 23rd, 2016
The Collective Impact Forum & Results for America present a panel discussion to celebrate the release of "Community Engagement Matters (Now More Than Ever)," an article co-authored by Melody Barnes and Paul Schmitz, published in the Spring issue of the Stanford Social Innovation Review. The article features original research that highlights the importance of engaging community when implementing data-driven, evidence-based approaches and provides a framework for how to do so effectively.
John Kania, Managing Director, FSG
learn more http://collectiveimpactforum.org/
January 21st, 2016
Introduction: Large-scale distributed data networks consisting of diverse stakeholders including providers, patients, and payers are changing health research in terms of methods, speed and efficiency. The Vaccine Safety Datalink (VSD) set the stage for expanded involvement of health plans in collaborative research Learn more
January 7th, 2016
Engaging community members in problem-solving solutions to issues that affect them is one of the fundamental principles of public health. The most effective way to achieve public health goals, especially the elimination of disparities in health status, is to actively engage those experiencing the problems in every aspect of addressing them. Community engagement means involving community members in all activities--from identifying the relevant issues and making decisions about how to address them, to evaluating and sharing the results with the community. The information on this Web site provides background, tips and tools for effective community engagement.
November 6th, 2015
A Comparison of Six Survey Methods to Capture Racial Identity
Consider, for example, a man whose mother is Asian and whose father is white. This may seem like someone who could easily be categorized as multiracial. But if this man was raised with little or no interaction with his white relatives or had experiences that were more closely aligned with those of the Asian community, he may well select â€śAsianâ€ť and nothing else when describing his race. Furthermore, some adults may have relatives of different races farther back in their family tree. While some people may think to include a more distant relative of a different race when asked about their racial background, others may not, even if they are aware of their family history.
With this in mind, we set out to test six different ways of defining a population of mixed-race adults to survey, using as our primary vehicle Pew Research Centerâ€™s American Trends Panel (ATP), a probability-based, nationally representative online panel of adults in the United States. We tested these different approaches with impaneled individuals who participated in more than one Pew Research Center survey, allowing us to examine how the same individual might have changed his or her responses depending on the question asked.
September 30th, 2015
Discuss a National Topic: Marijuana use Among youth https://t.co/UkjRmRyGQe
— Community Engagement (@mayoclinic_cenr) September 30, 2015
September 22nd, 2015
Join us on September 24
OCOH is a town hall meeting series that shares innovative research findings to foster conversation and mutual understanding with the community.
our participate on twitter using the the #OCOH hashtag
August 28th, 2015
Victor Montori has a very special light fixture in his office.
Co-workers say Montoriâ€™s Get-the-Party-Started accessory first appeared sometime after Christmas. The Mayo endocrinologist and world-traveling proponent of kinder and more careful medicine had just relocated his team of scientists to a new workspace. The Plummer Building! An open floor plan! White boards for brainstorming sessions, a Keurig machine, couch, and Nerf basket! But it was a little small. â€śYou know what would make this place great?â€ť he declared. â€śA disco ball!â€ť read more
August 13th, 2015
ACHLA-The Alliance of Chicanos Hispanics and Latin Americans, will host a free LATINO FEST and celebration on Saturday, September 26,on the Cooke park (seventh St and seventh Ave NW Rochester MN).
From 1:00 pm to 6:00 pm. rain or shine
August 5th, 2015
Liver cancer is the leading cause of cancer-related death among African men and the third leading cause among African women, according to the American Cancer Society. Two Mayo researchers with roots on the continent are working to make sure those numbers go down, and they're starting with the Somali community in Rochester.
After growing up and attending medical school in his native Ghana, Lewis Roberts, M.B., Ch.B., Ph.D., pursued his Ph.D. at the University of Iowa, reports the Rochester Post-Bulletin. Dr. Roberts then was accepted into Mayo Clinic's "highly selective" Clinical and Translational Science program, where he "received training to both practice as a clinician and do robust research work." After graduating, Dr. Roberts set his sights on treating and researching liver cancer "because of its prevalence in Africa."