We have a system in the U.S. that is designed to make sure that research involving people is held to high ethical standards. Researchers that propose to conduct studies involving people must have their studies reviewed and approved by a research ethics board before a study may begin. These boards, known as Institutional Review Boards (IRBs) are usually based at universities and other research institutions, and usually look at the risks and benefits to individuals participating in research. They are not designed to look at the risks and benefits to the communities involved. As more communities and community-based organizations get involved in research ? either as partners with academic researchers or as researchers themselves ? they are establishing their own IRBs and research review committees to make sure that the research is ethical and takes into account the risks and benefits to both individuals and communities. As documented in recent studies, these community IRBs and research review committees hold great promise for promoting ethical research and ensuring that the concerns of communities are adequately addressed by research. To support this emerging field of practice and research, a community-based organization in Los Angeles that manages its own IRB and a national organization in Raleigh that builds community capacity for research are jointly proposing a conference to convene community IRBs and research review committees from across the country to learn from one another; review the research about them that does exist; and identify priorities for research, practice and policy.

Public Health Relevance

Community-engaged research is recognized by the National Institutes of Health, researchers and community groups as being critical to achieving health equity across diverse communities in the United States. Because it involves community members and community-based organizations in research, community-engaged research is not only concerned about the risks and benefits to individual study participants, but to the involved communities as well. By convening community groups from across the country that operate boards that examine the risks and benefits of research and whether studies are feasible, community-responsive and culturally appropriate, the proposed conference helps to ensure that community-engaged research in the future can reach its full potential to improve the public's health.

Agency
National Institute of Health (NIH)
Institute
National Institute on Minority Health and Health Disparities (NIMHD)
Type
Conference (R13)
Project #
2R13MD008673-03
Application #
9332053
Study Section
Special Emphasis Panel (ZMD1)
Program Officer
Jones, Nancy Lynne
Project Start
2017-08-11
Project End
2019-01-31
Budget Start
2017-08-11
Budget End
2019-01-31
Support Year
3
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Community-Campus Partnerships/Health
Department
Type
DUNS #
167028559
City
Seattle
State
WA
Country
United States
Zip Code
98105