Perceptions Community Residents Have about Partner Institutions and Clinical Research
Version of Record online: 18 OCT 2013
© 2013 Wiley Periodicals, Inc.
Clinical and Translational Science
Volume 6, Issue 6, pages 469–473, December 2013
How to Cite
Kennedy, B. M., Katzmarzyk, P. T., Johnson, W. D., Griffin, W. P., Kennedy, K. B., Cefalu, W. T. and Ryan, D. H. (2013), Perceptions Community Residents Have about Partner Institutions and Clinical Research. Clinical and Translational Science, 6: 469–473. doi: 10.1111/cts.12120
- Issue online: 13 DEC 2013
- Version of Record online: 18 OCT 2013
- National Institute of General Medical Sciences
- National Institutes of Health
Engaging community residents to obtain their feedback in conducting clinical research, and including them as leaders in implementing applicable health advances is crucial for success and sustaining large center awards.
Forty-four adult men and women participated in one of four focus groups. Two groups each (one African American and one Caucasian) were conducted in Baton Rouge and in New Orleans.
In an effort to determine the knowledge, attitudes, and beliefs Louisiana residents have about the Louisiana Clinical and Translational Science (LA CaTS) Center concept, four main themes emerged from focus group participants concerning the state's research institutions, and what it means to have these institutions operating under one umbrella to improve the quality of health of its people: (1) academic/research institutions of the State are uniformly widely recognized and held in high regard; (2) increasing awareness of clinical research is a necessity; (3) establishing the LA CaTS Center is an excellent idea; and (4) effective communication including delivery style is crucial to partnerships and especially to the community.
Focus group discussions can provide insight into community residents’ perceptions, beliefs, motivations, and patterns of behavior for strategically planning for large center awards.