Few studies have gathered systematic information from either patient or non-patient populations on functioning and well-being within specific ethnic groups, leaving us with inadequate information on the adequacy and appropriateness of available measurement tools in minority groups. Appropriate assessment of functional status and other health constructs are essential in development of strategies to address racial disparities in chronic diseases. We hypothesize that ethnic groups (focusing here on black and white) will differ: On the criteria members use to define functional limitation On the importance ascribed to criteria such as physical activity or role functioning. On the criteria used to define """"""""well-being"""""""" and the value placed on specific behavioral, cognitive, and other characteristics. We propose to use previously collected data from a qualitative study: """"""""Ethnicity and Functioning in Boston Communities."""""""" We will focus on the relationships and significance from qualitative data for a commonly used measure of function: the SF-36. The 2-3 hour, taped interviews with 65 adults from different ethnic groups, many with chronic diseases, will be analyzed using qualitative and quantitative methods. These community-based individuals received the SF-36, measures of ethnic identification, and a measure of sense of control, as well as a detailed discussion of the meaning of the concepts assessed within these measures to them. We will use QSR*-NUDIST-4 (a text analysis computer software program) to organize the interview data text for subsequent interpretation. We will use the results from this detailed qualitative analysis to inform a quantitative analysis of the Medical Expenditure Panel Survey (MEPS), examining racial importance of ethnicity in defining functional health status and sense of well being; examine how these might importance of ethnicity and defining functional health status and sense of well being; examine how these might vary by social class and gender; and explore the need for more accurate representation of ethnicity in research.

Agency
National Institute of Health (NIH)
Institute
Agency for Healthcare Research and Quality (AHRQ)
Type
Research Program Projects (P01)
Project #
5P01HS010861-02
Application #
6492335
Study Section
Special Emphasis Panel (ZHS1)
Project Start
2001-09-01
Project End
2002-08-31
Budget Start
Budget End
Support Year
2
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Torrone, Elizabeth A; Levandowski, Brooke A; Thomas, James C et al. (2010) Identifying gaps in HIV prevention services. Soc Work Public Health 25:327-40
Do, Young Kyung; Carpenter, William R; Spain, Pamela et al. (2010) Race, healthcare access and physician trust among prostate cancer patients. Cancer Causes Control 21:31-40
Spain, Pamela; Carpenter, William R; Talcott, James A et al. (2008) Perceived family history risk and symptomatic diagnosis of prostate cancer: the North Carolina Prostate Cancer Outcomes study. Cancer 113:2180-7
Talcott, James A; Spain, Pamela; Clark, Jack A et al. (2007) Hidden barriers between knowledge and behavior: the North Carolina prostate cancer screening and treatment experience. Cancer 109:1599-606
Carey, Timothy S; Howard, Daniel L; Goldmon, Moses et al. (2005) Developing effective interuniversity partnerships and community-based research to address health disparities. Acad Med 80:1039-45
Chen, Ian; Kurz, James; Pasanen, Mark et al. (2005) Racial differences in opioid use for chronic nonmalignant pain. J Gen Intern Med 20:593-8