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1.
Soc Work Public Health ; 24(4): 305-29, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19517298

RESUMO

The Radiation Oncology Community Outreach Group (ROCOG) and the Neighborhood Cancer Care Cooperative (NCCC) were developed to address oncology-related health disparities utilizing a community-based, collaborative organizational design. Funded in 2003 by the National Cancer Institute's Cancer Disparities Research Partnership program, ROCOG/NCCC has focused on reducing barriers to care and enhancing the health care system's responsiveness to minority and indigent populations within Southwestern Pennsylvania. This article will describe the component programs that have been developed under this umbrella, as well as the evolved administrative, governance, and evaluation infrastructure that supports these initiatives.


Assuntos
Institutos de Câncer/organização & administração , Serviços de Saúde Comunitária/organização & administração , Relações Comunidade-Instituição , Neoplasias/terapia , Desenvolvimento de Programas/métodos , Pesquisa sobre Serviços de Saúde , Humanos , Modelos Teóricos , National Cancer Institute (U.S.) , Pennsylvania , Avaliação de Programas e Projetos de Saúde , Garantia da Qualidade dos Cuidados de Saúde , Radioterapia (Especialidade)/organização & administração , Estados Unidos
2.
Soc Work Public Health ; 24(4): 330-54, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19517299

RESUMO

The Radiation Oncology Community Outreach Group (ROCOG) and Neighborhood Cancer Care Cooperative (NCCC) were funded by the National Cancer Institute Radiation Research Program Cancer Disparities Research Partnership program in September 2003. ROCOG/NCCC provides customized, community hospital-based initiatives intended to help close the cancer disparities gap. In our two preceding articles in this issue, we have explored contextual and organizational development, described infrastructure and component programs, and outlined early evaluation strategies. This article will conclude the series of publications describing our early development by evaluating the formative implementation phase of the project. Our first 12 months were initially evaluated through a survey designed to assess staff and key stakeholders' perception of progress. An assessment of the level of completion of key project tasks was conducted 6 months after the survey. This combination has allowed ROCOG/NCCC to determine areas of success and also illustrate those in need of improvement. Our evaluation strategy can also serve as an efficient and inexpensive model for other similar community-based start-up programs to replicate.


Assuntos
Institutos de Câncer/organização & administração , Relações Comunidade-Instituição , Neoplasias/terapia , Desenvolvimento de Programas , Radioterapia (Especialidade)/organização & administração , Pesquisa sobre Serviços de Saúde , Humanos , Entrevistas como Assunto , Participação do Paciente , Serviços Preventivos de Saúde/métodos , Serviços Preventivos de Saúde/normas , Qualidade da Assistência à Saúde , Características de Residência
3.
Infect Agent Cancer ; 4 Suppl 1: S15, 2009 Feb 10.
Artigo em Inglês | MEDLINE | ID: mdl-19208206

RESUMO

BACKGROUND: It has been noted that the African American population in the U.S. bears disproportionately higher cancer morbidity and mortality rates than any racial and ethnic group for most major cancers. Many studies also document that decreased longevity is associated with low educational attainment and other markers of low socioeconomic status (SES), both of which are prevalent in African American communities across the nation. Evidence suggests that this phenomenon may be due to attitudes that reflect a lack of knowledge surrounding facts about cancer awareness and prevention. This study was designed to yield data concerning the general population's attitudes toward cancer, taking into consideration racial and/or socioeconomic differences in the population studied. RESULTS: Two hundred and fifteen subjects participated in the survey, of which 74% (159/215) defined themselves as African-American, 20% were White, and 6% were of other races. While only 38% of the study population was able to identify at least 5 risk factors associated with cancer, a lower proportion of African Americans identified at least 5 risk factors than whites (34% vs. 53%, p = 0.03). In addition, a slightly higher percentage of African Americans (10%) were not aware of the definition of a clinical trial when compared to whites (8%, p > 0.1). Of those aware of the definition of a clinical trial, African Americans were more reluctant to participate in clinical trials, with 53% answering no to participation compared to 15% of whites (p = 0.002). CONCLUSION: When comparing results to a similar study conducted in 1981, a slight increase in cancer knowledge in the African American population was observed. Our results suggest that while knowledge of cancer facts has increased over the years amongst the general population, African Americans and lower income populations are still behind. This may affect their risk profile and cancer early detection.

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