Community Engagement

The Community Engagement (CE) Program is located in the OSU College of Public Health, and is part of the OSU Center for Clinical and Translational Science (CCTS).

The infrastructure we are building through the CCTS for community engagement in research includes two primary components: 1) practice-based research network; and 2) community-based research network. OSU has an established Primary Care Practice-based Research Network (PC PBRN). The CE Program promotes the PC PBRN as a resource for research ideas, participant recruitment, and dissemination. We are also developing a Community-based Research Network (CBRN) that will make it easier for researchers to engage with diverse community partners in the research process.

The CE Program at OSU started in summer, 2008. Specific activities planned for the first year include:

  • Competitive pilot grants for community-engagement in research.
  • Community research capacity building with existing community-based networks affiliated with OSU.
  • Experiential opportunities for secondary students to learn about clinical and translational research.
  • Education for researchers about “community engagement in research” through seminars and website.

The leadership for the CE Program includes:

  • Director: Mary Ellen Wewers, PhD, MPH, Professor and Associate Dean for Research, College of Public Health
  • Co-director: Kelly Kelleher, MD, MPH, Director, Center for Innovation in Pediatric Practice and Vice President for Health Services Research, Nationwide Children’s Hospital.
  • Associate directors: Larry Gabel, PhD, Vice Chair, Family Medicine & Electra Paskett, PhD, Professor, College of Public Health

For more information, contact Nancy Hood, MPH, the CE Program Manager, nhood@cph.osu.edu, 614-688-3478.

Federal health agencies (e.g., CDC, NIH, AHRQ) are increasingly recognizing, supporting, and in many cases requiring “community engagement” in health-related research. Evidence shows that community involvement can increase the relevance and quality of health research, even in clinical studies.

Challenges exist, however, in defining what “community engagement” actually means for research practice. It is often easier to give examples of community engagement in research than to define it. Here are a few examples:

  • A cancer survivor participates in a university’s Institutional Review Board (IRB) to provide a community perspective when research applications are reviewed.
  • A university-based researcher partners with clinicians in community-based behavioral health clinics to implement a mental health intervention shown to be effective in more controlled settings.
  • A university-based researcher partners with the medical director of a health system in Appalachia Ohio to determine whether a brief intervention to help patients stop smoking is possible in that setting.
  • A community-based education program asks health researchers to help them evaluate the impact of a diabetes self-management program.

There are different “levels” of community participation in research. Community-based participatory research (CBPR) is on one end of the “engagement” spectrum (Israel et al., 2005). This end of the spectrum is described as equal participation by community partners and researchers throughout the research process.

On the other end of the spectrum, communities are simply informed about what research is occurring, and what the results were. In the middle of the spectrum, communities are engaged in important but limited aspect of research studies, such as recruiting and retaining research participants. It is important to recognize that more participation is not always better; some community partners may not have the time, interest, or expertise to participate as equal partners in every stage of the research process (Green, 2003).

The CE Program defines “community” broadly to include community residents, community-based organizations, public health agencies, social service providers, healthcare providers, healthcare payers, or elected officials. Communities can further be defined based on age, geography, race, ethnicity, disease, gender, sexual orientation, or other defining characteristics. Community partners or representatives may be involved in any or all steps in the research process, including but not limited to:

  • identifying health concerns
  • prioritizing research questions
  • designing a study
  • recruiting and retaining study participants
  • designing data collection instruments and protocols
  • collecting data
  • designing and implementing interventions
  • analyzing data
  • interpreting findings
  • disseminating findings
  • translating findings into practice

For more information, contact Nancy Hood, MPH, the CE Program Manager, nhood@cph.osu.edu, 614-688-3478.

Existing outreach and engagement resources at OSU

The Ohio State University (OSU) has numerous existing resources for community engagement and outreach – in fact, OSU received a new classification in 2008 called “Curricular Engagement and Outreach & Partnerships” from the Carnegie Foundation for the Advancement of Teaching. Many of these resources are well-kept secrets for investigators doing health-related research. For more information about these resources, please click on the links below or e-mail ccts-community@osumc.edu.

OSU Primary Care Practice-based Research Network (OSU-PCPBRN)


OSU Extension


OSU College of Pharmacy


OSU Outreach and Engagement Office


P12 Project


OSU researchers conducting community engaged research

Many OSU investigators already conduct research in and with communities. Investigators doing community-engaged research will be profiled here to facilitate networking and collaboration.

Assessment of community engagement in research

The CE Program is conducting an assessment to identify ways that communities are currently engaged in health-related clinical and translational research at OSU. The assessment includes two components:

  • A brief, on-line survey that will be e-mailed to principal investigators with NIH-funded studies active in the past five years.
  • Case studies of eight research projects illustrating different ways communities can be engaged in research. Projects will be identified through the on-line survey, an OSUToday announcement, and word of mouth. To recommend a project, please e-mail Nancy Hood, nhood@cph.osu.edu.

Please check back for assessment results in Spring 2009!

Do you need training or tools for conducting community-engaged research? There are many high-quality, user-friendly resources for researchers and community partners interested in this type of research. Browse the links below for training, education and advocacy organizations, community assessment tools, and evidence-based interventions.

Training in Community-engaged Research

A Skill-Building Curriculum for Community-based Participatory Research Partnerships


Research Ethics Training Curriculum for Community Representatives


Education and Advocacy for Engaging Communities in Research

Community-Campus Partnerships for Health


Education Network to Advance Cancer Clinical Trials (ENACCT)


Community Assessment

Appalachian Rural Health Institute


Central Ohio Data Access Tools


The Community Toolbox


Health Landscape


OASIS (Online Analysis and Statistical Information System)


Ohio Family Health Survey


Evidence-based Interventions

Guide to Community Preventive Services


Guide to Clinical Preventive Services