Abstract
Racial, ethnic and economic disparities in cancer rates, outcomes, and clinical trials participation persist despite significant research. We examined barriers to clinical trials enrollment among Chinese patients, and developed a navigation program for Chinese gynecologic and breast cancer patients. Six bilingual navigators were trained and a navigator assigned to each patient for at least 2 months. All patients received a clinical trials booklet in Chinese and English. Data collection included pre-and post-navigation surveys, intake forms, and documentation of navigation encounters. Between July 2010 and May 31, 2011, we recruited 28 breast and gynecologic cancer patients. Patients averaged 317 min of navigation (range 63–1,852) during 8 sessions (range 3–28). They improved in 4 of 10 true–false knowledge statements about clinical trials. A patient navigation program for Chinese-speaking cancer patients is feasible. It results in high patient satisfaction rates and modest improvements in clinical trials knowledge and participation.
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Acknowledgments
The research team is grateful to the following people: statistical assistance from Huey and Christine Yu; the long volunteering hours from the navigators: Lan Chen, Mei-Lin Cheng, Mei-Ling Li, Grace Yang, Lichen Wan, and Tammy Che; and to staff from Stanford: Maureen Sutton, Holly Gautier and Miriam Bischoff. This research was supported by a “2009 Developmental Cancer Research Award” from the Stanford Cancer Institute to Nelson Teng, and Stanford Hospital’s Guest Services.
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The authors have no conflict of interest.
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E. Clair McClung and Sharon Watkins Davis contributed equally as first authors.
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Clair McClung, E., Davis, S.W., Jeffrey, S.S. et al. Impact of Navigation on Knowledge and Attitudes About Clinical Trials Among Chinese Patients Undergoing Treatment for Breast and Gynecologic Cancers. J Immigrant Minority Health 17, 976–979 (2015). https://doi.org/10.1007/s10903-013-9901-x
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DOI: https://doi.org/10.1007/s10903-013-9901-x