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International Journal of Telemedicine and Applications
Volume 2012, Article ID 715194, 9 pages
http://dx.doi.org/10.1155/2012/715194
Research Article

How Do Low-Income Urban African Americans and Latinos Feel about Telemedicine? A Diffusion of Innovation Analysis

1Center for Biomedical Informatics, Charles R. Drew University of Medicine and Science, 2594 Industry Way, Lynwood, CA 90262, USA
2Department of Psychiatry, UCLA and VA Greater Los Angeles Healthcare System, 11301 Wilshire Boulevard, Los Angeles, CA 90073, USA
3College of Medicine, Charles R. Drew University of Medicine and Science, 1731 E. 120th Street, Los Angeles, CA 90059, USA

Received 13 January 2012; Accepted 31 July 2012

Academic Editor: Yunan Chen

Copyright © 2012 Sheba George et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. T. Greenhalgh, G. Robert, F. Macfarlane, P. Bate, and O. Kyriakidou, “Diffusion of innovations in service organizations: systematic review and recommendations,” Milbank Quarterly, vol. 82, no. 4, pp. 581–629, 2004. View at Publisher · View at Google Scholar · View at Scopus
  2. B. L. Chang, S. Bakken, S. S. Brown et al., “Bridging the digital divide: reaching vulnerable populations,” Journal of the American Medical Informatics Association, vol. 11, no. 6, pp. 448–457, 2004. View at Publisher · View at Google Scholar · View at Scopus
  3. A. Nelson, “Unequal treatment: confronting racial and ethnic disparities in health care,” Journal of the National Medical Association, vol. 94, no. 8, pp. 666–668, 2002. View at Google Scholar · View at Scopus
  4. K. A. Phillips, M. L. Mayer, and L. A. Aday, “Barriers to care among racial/ethnic groups under managed care,” Health Affairs, vol. 19, no. 4, pp. 65–75, 2000. View at Google Scholar · View at Scopus
  5. S. Shea, J. Starren, R. S. Weinstock et al., “Columbia University's Informatics for Diabetes Education and Telemedicine (IDEATel) Project: rationale and design,” Journal of the American Medical Informatics Association, vol. 9, no. 1, pp. 49–62, 2002. View at Google Scholar · View at Scopus
  6. D. R. Williams, “Race, socioeconomic status, and health the added effects of racism and discrimination,” Annals of the New York Academy of Sciences, vol. 896, pp. 173–188, 1999. View at Google Scholar · View at Scopus
  7. D. S. Puskin, “Opportunities and challenges to telemedicine in rural America,” Journal of Medical Systems, vol. 19, no. 1, pp. 59–67, 1995. View at Publisher · View at Google Scholar · View at Scopus
  8. W. C. Richardson, Crossing the Quality Chasm: A New Health System for the 21st Century, Institute of Medicine, Washington, DC, USA, 2001.
  9. P. S. Whitten, F. S. Mair, A. Haycox, C. R. May, T. L. Williams, and S. Hellmich, “Systematic review of cost effectiveness studies of telemedicine interventions,” British Medical Journal, vol. 324, no. 7351, pp. 1434–1437, 2002. View at Google Scholar · View at Scopus
  10. W. R. Hersh et al., Telemedicine for the Medicare Population: Update, Agency for Healthcare Research and Quality, Rockville, Md, USA, 2006.
  11. R. S. Baker, N. L. Watkins, M. R. Wilson, M. Bazargan, and C. W. Flowers, “Demographic and clinical characteristics of patients with diabetes presenting to an urban public hospital ophthalmology clinic,” Ophthalmology, vol. 105, no. 8, pp. 1373–1379, 1998. View at Publisher · View at Google Scholar · View at Scopus
  12. T. S. Nesbitt, D. M. Hilty, C. A. Kuenneth, and A. Siefkin, “Development of a telemedicine program,” Western Journal of Medicine, vol. 173, no. 3, pp. 169–174, 2000. View at Publisher · View at Google Scholar · View at Scopus
  13. E. L. Carter, G. Nunlee-Bland, and C. Callender, “A patient-centric, provider-assisted diabetes telehealth self-management intervention for urban minorities,” Perspectives in Health Information Management/AHIMA, American Health Information Management Association, 2011.
  14. K. Shahid, A. M. Kolomeyer, N. V. Nayak et al., “Ocular telehealth screenings in an urban community,” Telemedicine and e-Health, vol. 18, no. 2, pp. 95–100, 2012. View at Google Scholar
  15. N. Scheinfeld, M. Fisher, P. Genis, and H. Long, “Evaluating patient acceptance of a teledermatology link of an urban urgent-care dermatology clinic run by residents with board certified dermatologists,” SKINmed Journal, vol. 2, no. 3, pp. 159–162, 2003. View at Google Scholar
  16. P. M. Trief, R. Izquierdo, J. P. Eimicke et al., “Adherence to diabetes self care for white, African-American and Hispanic American telemedicine participants: 5 year results from the IDEATel project,” Ethnicity & Health. In press.
  17. R. S. Weinstock, J. A. Teresi, R. Goland et al., “Glycemic control and health disparities in older ethnically diverse underserved adults with diabetes: five-year results from the Informatics for Diabetes Education and Telemedicine (IDEATel) study,” Diabetes Care, vol. 34, no. 2, pp. 274–279, 2011. View at Publisher · View at Google Scholar · View at Scopus
  18. E. M. Rogers, Diffusion of Innovations, Free Press, 1995.
  19. A. Allen and J. Hayes, “Patient satisfaction with teleoncology: a pilot study,” Telemedicine Journal, vol. 1, no. 1, pp. 41–46, 1995. View at Google Scholar · View at Scopus
  20. H. Mekhjian, J. W. Turner, M. Gailiun, and T. A. McCain, “Patient satisfaction with telemedicine in a prison environment,” Journal of Telemedicine and Telecare, vol. 5, no. 1, pp. 55–61, 1999. View at Google Scholar · View at Scopus
  21. J. W. Turner, R. J. Thomas, and N. L. Reinsch Jr., “Willingness to try a new communication technology: perceptual factors and task situations in a health care context,” Journal of Business Communication, vol. 41, no. 1, pp. 5–26, 2004. View at Publisher · View at Google Scholar · View at Scopus
  22. R. L. Bashshur, “Public acceptance of telemedicine in a rural community,” Bioscience Communications, vol. 4, pp. 17–38, 1978. View at Google Scholar
  23. J. E. Brick, R. L. Bashshur, J. F. Brick, and R. M. D'Alessandri, “Public knowledge, perception, and expressed choice of telemedicine in rural West Virginia,” Telemedicine Journal, vol. 3, no. 2, pp. 159–171, 1997. View at Publisher · View at Google Scholar
  24. Department of Health Services, L.A.C., The Health of the Residents in South Service Planning Area of Los Angeles County, Los Angeles County Department of Health Services, 2007.
  25. Department of Health, Los Angeles County Health Survey, Department of Health, Los Angeles, Calif, USA, 2005.
  26. M. Agar and J. MacDonald, “Focus Groups and ethnography,” Human Organization, vol. 54, no. 1, pp. 78–86, 1995. View at Google Scholar
  27. R. A. Krueger and M. A. Casey, Focus Groups: A Practical Guide for Applied Research, Sage Publications, 2000.
  28. D. L. Morgan, Focus Groups as Qualitative Research, Sage Publications, 1997.
  29. D. W. Stewart, P. N. Shamdasani, and D. W. Rook, Focus Groups: Theory and Practice, Sage, 2007.
  30. A. L. Strauss, Qualitative Analysis for Social Scientists, Cambridge University Press, 1987.
  31. D. C. Alverson, B. Holtz, J. D'Iorio, M. Devany, S. Simmons, and R. K. Poropatich, “One size doesn't fit all: bringing telehealth services to special populations,” Telemedicine and e-Health, vol. 14, no. 9, pp. 957–963, 2008. View at Publisher · View at Google Scholar · View at Scopus
  32. M. Lillie-Blanton, M. Brodie, D. Rowland, D. Altman, and M. McIntosh, “Race, ethnicity, and the health care system: public perceptions and experiences,” Medical Care Research and Review, vol. 57, no. 1, pp. 218–235, 2000. View at Google Scholar · View at Scopus
  33. W. D. King, “Examining African Americans' mistrust of the health care system: expanding the research question,” Public Health Reports, vol. 118, no. 4, pp. 366–367, 2003. View at Google Scholar · View at Scopus
  34. T. A. LaVeist, K. J. Nickerson, and J. V. Bowie, “Attitudes about racism, medical mistrust, and satisfaction with care among African American and white cardiac patients,” Medical Care Research and Review, vol. 57, no. 1, pp. 146–161, 2000. View at Google Scholar · View at Scopus
  35. L. E. Boulware, L. A. Cooper, L. E. Ratner, T. A. LaVeist, and N. R. Powe, “Race and trust in the health care system,” Public Health Reports, vol. 118, no. 4, pp. 358–365, 2003. View at Google Scholar · View at Scopus
  36. V. N. Gamble, “Under the Shadow of Tuskegee: African Americans and Health Care,” American Journal of Public Health, vol. 87, no. 11, pp. 1773–1778, 1997. View at Google Scholar · View at Scopus
  37. S. B. Thomas and S. C. Quinn, “Public health then and now: the Tuskegee Syphilis Study, 1932 to 1972: implications for HIV education and AIDS risk education programs in the black community,” American Journal of Public Health, vol. 81, no. 11, pp. 1498–1504, 1991. View at Google Scholar · View at Scopus
  38. D. P. Scharf, K. J. Mathews, P. Jackson, J. Hofsuemmer, E. Martin, and D. Edwards, “More than Tuskegee: understanding mistrust about research participation,” Journal of Health Care for the Poor and Underserved, vol. 21, no. 3, pp. 879–897, 2010. View at Publisher · View at Google Scholar · View at Scopus
  39. R. BeLue, K. D. Taylor-Richardson, J. Lin, A. T. Rivera, and D. Grandison, “African Americans and participation in clinical trials: differences in beliefs and attitudes by gender,” Contemporary Clinical Trials, vol. 27, no. 6, pp. 498–505, 2006. View at Publisher · View at Google Scholar · View at Scopus
  40. D. F. Farmer, S. A. Jackson, F. Camacho, and M. A. Hall, “Attitudes of African American and low socioeconomic status white women toward medical research,” Journal of Health Care for the Poor and Underserved, vol. 18, no. 1, pp. 85–99, 2007. View at Publisher · View at Google Scholar · View at Scopus
  41. C. A. Gadegbeku, P. K. Stillman, M. D. Huffman, J. S. Jackson, J. W. Kusek, and K. A. Jamerson, “Factors associated with enrollment of African Americans into a clinical trial: results from the African American study of kidney disease and hypertension,” Contemporary Clinical Trials, vol. 29, no. 6, pp. 837–842, 2008. View at Publisher · View at Google Scholar · View at Scopus
  42. P. Herring, S. Montgomery, A. K. Yancey, D. Williams, and G. Fraser, “Understanding the challenges in recruiting blacks to a longitudinal cohort study: the adventist health study,” Ethnicity and Disease, vol. 14, no. 3, pp. 423–430, 2004. View at Google Scholar · View at Scopus
  43. V. A. Johnson, K. A. Edwards, S. L. Sherman et al., “Decisions to participate in fragile X and other genomics-related research: native American and African American voices,” Journal of Cultural Diversity, vol. 16, no. 3, pp. 127–135, 2009. View at Google Scholar · View at Scopus
  44. H. M. Linden, L. M. Reisch, A. Hart et al., “Attitudes toward participation in breast cancer randomized clinical trials in the African American community: a focus group study,” Cancer Nursing, vol. 30, no. 4, pp. 261–269, 2007. View at Publisher · View at Google Scholar · View at Scopus
  45. Y. R. Smith, A. M. Johnson, L. A. Newman, A. Greene, T. R. B. Johnson, and J. L. Rogers, “Perceptions of clinical research participation among African American women,” Journal of Women's Health, vol. 16, no. 3, pp. 423–428, 2007. View at Publisher · View at Google Scholar · View at Scopus
  46. S. B. Wyatt, N. Diekelmann, F. Henderson et al., “A community-driven model of research participation: the Jackson Hearth Study participant recruitment and retention study,” Ethnicity and Disease, vol. 13, no. 4, pp. 438–455, 2003. View at Google Scholar · View at Scopus
  47. M. P. Doescher, B. G. Saver, P. Franks, and K. Fiscella, “Racial and ethnic disparities in perceptions of physician style and trust,” Archives of Family Medicine, vol. 9, no. 10, pp. 1156–1163, 2000. View at Google Scholar · View at Scopus
  48. R. L. Johnson, S. Saha, J. J. Arbelaez, M. C. Beach, and L. A. Cooper, “Racial and ethnic differences in patient perceptions of bias and cultural competence in health care,” Journal of General Internal Medicine, vol. 19, no. 2, pp. 101–110, 2004. View at Publisher · View at Google Scholar · View at Scopus
  49. S. Saha, J. J. Arbelaez, and L. A. Cooper, “Patient-physician relationships and racial disparities in the quality of health care,” American Journal of Public Health, vol. 93, no. 10, pp. 1713–1719, 2003. View at Google Scholar · View at Scopus