A crowd-sourced collection of resources for population health scientists, practitioners and policy-makers. Click each topic below to see the resources currently available.
Resources for researchers interested in knowledge exchange. This includes a knowledge exchange toolkit; profiles of ten knowledge exchange projects, and websites and articles with more information. These materials are provided by the Population Health Institute at the University of Wisconsin for anyone interested in knowledge exchange with partners such as community groups, policymakers, and government organizations who are seeking strategies to improve population health.
Training in Interdisciplinary Health Science: Current Successes and Future Needs. This report, commissioned by the IOM Roundtable on Population Health Improvement, offers a vision and specific recommendations for future training in interdisciplinary population health science based on a June 1-2, 2015 meeting of population health leaders at the Institute of Medicine in Washington DC.
RWJF Health & Society Scholars video, highlighting various aspects of population health research, communication, and application. Individual clips may also be downloaded free of charge and include:
- What is Population Health?(3 Minutes)
- Searching for Solutions(HSS Scholar Research) (5 Minutes)
- Race & Inequality(Courtney Cogburn & Patrick Sharkey) (25 Minutes)
- Asthma & Big Data(David Van Sickle) (25 Minutes)
- Using Media to Influence Policy(Mehret Mandefro) (5 Minutes)
- Community Development(Doug Jutte) (4 Minutes)
Building the Science of Population Health: The Robert Wood Johnson Foundation Health & Society Scholars Program 2001–2016 and Beyond. This report summarizes how the Health & Society Scholars (HSS) program was carried out and highlights lessons learned based on 13 years of experience in producing interdisciplinary population health scientists. The report, written by Kristin Harper on the basis of interviews with HSS participants, faculty, advisors, and funders as well as extensive documentation about the program’s operations over its lifetime, is also available in Executive Summary form.
Podcast: Having Friends, Socializing as Important to Good Health as Diet, Exercise The Population Reference Bureau interviews researcher Kathleen Mullan Harris about how social connections affect specific health measures.
Webinar: What’s Next for Integrated Population, Health, and Environment (PHE) and Family Planning? On Dec. 13 the PACE Project hosted an Africa PHE quarterly webinar with guest speaker, Teresa Casale, senior advocacy associate at PAI, to discuss how President Trump’s administration may impact U.S. government global funding for family planning and reproductive health.
Health Disparities Tool: The Office of Disease Prevention and Health Promotion (ODPHP) partnered with the National Center for Health Statistics (NCHS) and the Office of Minority Health (OMH) to expand DATA2020, the HealthyPeople.gov data search function, to include a tool that shows health disparities information for measurable, population–based objectives where data are available. Use the health disparities tool on DATA2020. For more information, click here.
Global Health Data Exchange (GHDx). The GHDx is comprehensive catalog of health and demographic datasets from around the world, including surveys, censuses, vital statistics, and other health-related data. The goal of the GHDx is to help people locate data by cataloging information about data including the topics covered, by providing links to data providers or explaining how to acquire the data, and in cases where we have permission, providing the data directly for download. Use the GHDx to research population census data, surveys, registries, indicators and estimates, administrative health data, and financial data related to health. Data made available for download by IHME can be used, shared, modified, or built upon via the Open Data Commons Attribution License.
2014 Native Hawaiian and Pacific Islander National Health Interview Survey (NHPI NHIS) Data. This is the first federal survey designed exclusively to measure the health of the civilian noninstitutionalized Native Hawaiian and Pacific Islander population of the United States. It was conducted by the National Center for Health Statistics using the standard 2014 NHIS survey instrument.
County Health Rankings. A collaboration between the Robert Wood Johnson Foundation and University of Wisconsin Population Health Institute, the annual County Health Rankings rank the health of nearly every county in the US and also provide measures of vital health factors, including high school graduation rates, obesity, smoking, unemployment, access to healthy foods, the quality of air and water, income inequality, and teen births in nearly every county in America. The program also provides Roadmaps that provide guidance and tools to understand the data, and strategies that communities can use to move into action.
The Mexican Health and Aging Study (MHAS) Announces Release of New Data: Wave 4 (2015). MHAS was designed to prospectively evaluate the impact of disease on the health, function and mortality of adults over the age of 50 in both urban and rural areas of Mexico. Data available in English and Spanish.
Performance, Monitoring and Accountability 2020 (PMA2020): PMA2020 uses mobile devices to routinely gather nationally and sub-nationally representative data on family planning and water and sanitation.
INDEPTH Network is a network of health and demographic surveillance systems in low-income and middle-income countries. The network maintains a freely accessible repository which includes health and demographic data from 20 sites covering 11 countries, 1.3 million individuals and over 5.3·million person-years of observations.
500 Cities Project. Data on 27 chronic disease measures, health outcomes, and clinical preventive service use for the 500 largest U.S. cities is available on-line thanks to a collaboration among the CDC, the CDC Foundation and the Robert Wood Johnson Foundation. An interactive website provides the ability to retrieve, visualize, and explore uniformly-defined city and census tract-level data. The data are derived from small area estimates.
HealthLandscape is an interactive web atlas that brings together various sources of health, socio-economic and environmental information in a convenient, central location. Part of the American Academy of Family Physicians, the site makes data and mapping tools freely available to the public, with applications related to health workforce & medical education, population indicators, and community data portals . A few examples of the many tools it offers:
- The Children’s Health and Education Mapping Tool supports data-driven decision-making by allowing users to search, map, download, and compare county-level data.
- The Social Determinants of Health (SDOH) Mapper is a cold-spotting tool that can assist in identifying areas of need.
- The Accountable Care Organization (ACO) Quality Explorer is an interactive mapping tool that presents data for 211 ACOs taking part in the Medicare Shared Savings Program (MSSP). The ACO Explorer allows users to visualize 33 quality metrics across five domains.
- View all the available resources at http://www.healthlandscape.org/live-Applications.cfm. HealthLandscape also offer free webinars http://www.healthlandscape.org/webinar-training.cfm for many of these tools and has a HealthLandscape Project 500 Cities Mapping Tool, http://www.healthlandscape.org/500Cities.
Guide for the establishment of health observatories. This publication from the World Health Organization’s Regional Office for Africa provides guidance for the creation of health observatories which gather, analyze, synthesize and share reliable and quality health information on population health and health services. Released April 2016.
Malawi Journals Project: Data now available for public use. These ethnographic journals written by local participant observers between 1999 and the present provide a unique perspective on the responses of rural Malawians to the AIDS epidemic.
- New PHS Human Subject and Clinical Trial Information form. Required for application due dates of January 25, 2018, and beyond.
- Current NIH definition of a clinical trial. Clarified and broadened in 2014, the definition encompasses a wide range of trial types: mechanistic, exploratory/developmental,pilot/feasibility, behavioral, and more.
- NIH policy changes related to enhancing stewardship of clinical trials, including requirement to apply to an FOA that specifically allows for the submission of clinical trial applications, training expectations, and peer review criteria.
Methodspace – From SAGE Publishing, this is a site called that offers a blog, videos, opportunities and more related to a variety of topics in social science methods. Recent offerings address use of social media, data visualization, mixed methods, “the methodology of inequality,” and more.
HHS Announces Final Changes to Human Subjects Research Regulations: see the final text for changes to the Common Rule.
New NIH Clinical Trials Policies: what are the implications for behavioral and social sciences research? Read the blog post from the Director of the NIH Office of Behavioral and Social Sciences research.
eLearning Course: Good Clinical Practice for Social and Behavioral Research. Aimed at NIH grantees.
Symbioses is an interdisciplinary research network that connects life scientists, social scientists, and humanities scholars working at the nexus of biology and social life. The group hosts periodic meetings, shares resources, and maintains a mailing list. Check out their website and click on the membership page to add your name to the mailing list.
The Science of Team Science (SciTS) is a program established by the National Cancer Institute to build the knowledge base for effective team science. The program developed a toolkit for team science and holds annual conferences.
HealthEquityGuide.org: This website from Human Impact Partners provides 25+ case studies of how health departments across the country have concretely advanced health equity. The site is structured around a set of strategic practices that can guide health departments (and their partners) down their unique path. The practices are organized by the following themes:
- Working across government
- Building internal infrastructure
- Fostering community partnerships
- Championing transformative change
Policy Communication Toolkit. This toolkit consolidates tools, materials, and approaches that the Population Reference Bureau has developed and refined over 30 years of training researchers to communicate to policy audiences. A product of the USAID-funded Policy, Advocacy, and Communications Enhanced for Population and Family Planning (PACE) Project. Watch a webinar about how to use the toolkit.