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Volumn 120 Suppl 7, Issue , 2014, Pages 1113-1121
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Five National Cancer Institute-designated cancer centers' data collection on racial/ethnic minority participation in therapeutic trials: a current view and opportunities for improvement.
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Author keywords
[No Author keywords available]
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Indexed keywords
ANCESTRY GROUP;
ARTICLE;
CANCER CENTER SUPPORT GRANT;
CANCER REGISTRY;
CATCHMENT AREA;
CLINICAL TRIAL (TOPIC);
DATA DEFINITIONS;
ETHNOLOGY;
FEMALE;
HEALTH CARE DELIVERY;
HEALTH CARE DISPARITY;
HEALTH DISPARITY;
HUMAN;
METHODOLOGY;
MINORITY ENROLLMENT;
MINORITY GROUP;
NATIONAL HEALTH ORGANIZATION;
NEOPLASM;
PATIENT SELECTION;
POVERTY;
QUANTITATIVE DATA;
RESIDENTIAL CARE;
SOCIOECONOMICS;
UNITED STATES;
VULNERABLE POPULATION;
CANCER CENTER SUPPORT GRANT;
CATCHMENT AREA;
CLINICAL TRIALS;
DATA DEFINITIONS;
HEALTH DISPARITIES;
MINORITY ENROLLMENT;
QUANTITATIVE DATA;
CATCHMENT AREA (HEALTH);
CLINICAL TRIALS AS TOPIC;
CONTINENTAL POPULATION GROUPS;
FEMALE;
HEALTH SERVICES ACCESSIBILITY;
HEALTHCARE DISPARITIES;
HUMANS;
MINORITY GROUPS;
NATIONAL CANCER INSTITUTE (U.S.);
NEOPLASMS;
PATIENT SELECTION;
POVERTY;
RESEARCH DESIGN;
SEER PROGRAM;
SOCIOECONOMIC FACTORS;
UNITED STATES;
VULNERABLE POPULATIONS;
WOMEN;
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EID: 84900032336
PISSN: None
EISSN: 10970142
Source Type: Journal
DOI: 10.1002/cncr.28571 Document Type: Article |
Times cited : (33)
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References (0)
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