8 results
Search Results
2. A National Collaborative for Building the Field of Childhood Obesity Research.
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Writing Group for the National Collaborative on Childhood Obesity Research (NCCOR). Electronic address: rachel.ballard@nih.gov and Writing Group for the National Collaborative on Childhood Obesity Research (NCCOR)
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PREVENTION of childhood obesity , *COMPARATIVE studies , *ELECTRONIC data interchange , *EPIDEMIOLOGY , *RESEARCH methodology , *MEDICAL cooperation , *MEDICAL research , *CHILDHOOD obesity , *RESEARCH , *EVALUATION research - Abstract
Rising rates of childhood obesity over the past 2 decades have spurred a number of public- and private-sector initiatives aimed at halting or even reversing this trend. Recognizing common interests in this issue, the Centers for Disease Control and Prevention, NIH, and the Robert Wood Johnson Foundation began conversations about creating a formal collaboration aimed at accelerating efforts to address childhood obesity by coordinating research agendas and providing support for evidence-building activities. The National Collaborative on Childhood Obesity Research (NCCOR) was launched in February 2009, and the U.S. Department of Agriculture joined in 2010. Using the model provided by other previously successful collaborations, such as the Youth Tobacco Cessation Collaborative, NCCOR has emphasized several principles suggested by Petrovich as key elements for successful partnerships: (1) delineate a common purpose by identifying key knowledge gaps in the field; (2) create a shared identity around that common purpose; (3) develop structures for democratic and respectful collaboration so as to strategically coordinate efforts for maximum national impact; (4) identify effective leaders capable of articulating challenges in the field and inspiring a commitment of minds and the resolve to address identified needs; (5) facilitate continuous knowledge exchange and synthesis to keep the field informed; and (6) support assessment of progress and feedback loops for ensuring continual progress. This paper examines how NCCOR has used these principles to help build the field of research, evaluation, and surveillance for childhood obesity prevention and management. [ABSTRACT FROM AUTHOR]
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- 2018
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3. Connecting the Dots: Linking the National Program of Cancer Registries and the Needs of Survivors and Clinicians.
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Ryerson, A Blythe, Eheman, Christie, Styles, Timothy, Rycroft, Randi, and Snyder, Claire
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CANCER patients , *PUBLIC health research , *CANCER diagnosis , *ACQUISITION of data , *CANCER , *COMMUNICATION , *MEDICAL protocols , *MEDICAL research , *HEALTH outcome assessment , *PUBLIC health , *RESEARCH funding , *TUMORS , *PATIENT selection - Abstract
Cancer survivors, the medical community, public health professionals, researchers, and policymakers all need information about newly diagnosed cancer cases and deaths to better understand and address the disease burden. CDC collects cancer data on 96% of the U.S. population through the National Program of Cancer Registries. The National Program of Cancer Registries routinely collects data on all cancer occurrences, deaths, and the types of initial treatment received by the patients, and recently CDC has made advances in its cancer surveillance activities that have direct applicability to cancer survivorship research and care. This article examines CDC's innovative uses of the National Program of Cancer Registries infrastructure and data as a recruitment source for survivorship research studies and behavioral interventions; comparative effectiveness and patient-centered outcomes research; and the collection, consolidation, and dissemination of treatment summaries for cancer survivors and their providers. This paper also discusses long-term, idealistic plans for additional data linkages and sharing among public health, providers, and the cancer survivor through innovative concepts such as patient portals and rapid-learning health care. [ABSTRACT FROM AUTHOR]
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- 2015
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4. Assessing the Value of Team Science: A Study Comparing Center- and Investigator-Initiated Grants
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Hall, Kara L., Stokols, Daniel, Stipelman, Brooke A., Vogel, Amanda L., Feng, Annie, Masimore, Beth, Morgan, Glen, Moser, Richard P., Marcus, Stephen E., and Berrigan, David
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RESEARCH grants , *MEDICAL research , *COOPERATIVE research , *RESEARCH institutes , *ACQUISITION of data , *LONGITUDINAL method , *COMPARATIVE studies - Abstract
Background: Large cross-disciplinary scientific teams are becoming increasingly prominent in the conduct of research. Purpose: This paper reports on a quasi-experimental longitudinal study conducted to compare bibliometric indicators of scientific collaboration, productivity, and impact of center-based transdisciplinary team science initiatives and traditional investigator-initiated grants in the same field. Methods: All grants began between 1994 and 2004 and up to 10 years of publication data were collected for each grant. Publication information was compiled and analyzed during the spring and summer of 2010. Results: Following an initial lag period, the transdisciplinary research center grants had higher overall publication rates than the investigator-initiated R01 (NIH Research Project Grant Program) grants. There were relatively uniform publication rates across the research center grants compared to dramatically dispersed publication rates among the R01 grants. On average, publications produced by the research center grants had greater numbers of coauthors but similar journal impact factors compared with publications produced by the R01 grants. Conclusions: The lag in productivity among the transdisciplinary center grants was offset by their overall higher publication rates and average number of coauthors per publication, relative to investigator-initiated grants, over the 10-year comparison period. The findings suggest that transdisciplinary center grants create benefits for both scientific productivity and collaboration. [Copyright &y& Elsevier]
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- 2012
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5. Global Health for Undergraduates: “We Are Not Alone”
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Barbiero, Victor K.
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MEDICAL school curriculum , *MEDICAL education , *PUBLIC health education , *PATHOGENIC microorganisms , *MEDICAL research - Abstract
Abstract: This paper presents a review of an undergraduate global health curriculum implemented at the George Washington University School of Public Health and Health Services. It is in concert with the framework and principles of the Association of American Colleges and Universities and their vision of Shared Futures of Global Learning and Social Responsibility. The rationale for a deep and broad undergraduate public health curriculum, which includes a global health component, is clear. Global health is a necessary and timely pathway for undergraduate liberal arts education. The world has dramatically changed in the past 50 years, and undergraduate education must continue to keep pace with these changes. Pathogens will adapt to changing ecologies, demographics, disease burdens, and population distributions. They are able to cross the world in hours or days. No country is invulnerable to disease importation and consequent indigenous transmission. Broad epidemic preparedness is required across all academic disciplines from epidemiology to sociology, from medicine to economics. Global health is anchored in the complementary application of various disciplines effectively joined to address a particular problem and mitigate potential adverse consequences. Our students recognize the reality of this interconnected world and are eager to take their place as global citizens. Knowledge, understanding, technical acumen, and humility represent the foundation of the global citizenry required to address the changing global pattern of disease worldwide. Undergraduate public health, and particularly undergraduate global health, will enable our undergraduates to embark on a myriad of professional trajectories that include public health, medicine, biomedical research, law, policy, environmental studies, anthropology, economics, sociology and other disciplines. The “Y” Generation in the U.S. (individuals born between 1980 and 2000) is poised for action; we must give them the tools to succeed. [Copyright &y& Elsevier]
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- 2008
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6. Impact of the Cancer Prevention and Control Research Network: Accelerating the Translation of Research Into Practice.
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Ribisl, Kurt M., Fernandez, Maria E., Friedman, Daniela B., Hannon, Peggy A., Leeman, Jennifer, Moore, Alexis, Olson, Lindsay, Ory, Marcia, Risendal, Betsy, Sheble, Laura, Taylor, Vicky M., Williams, Rebecca S., and Weiner, Bryan J.
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CANCER prevention , *COLON cancer , *PAPILLOMAVIRUSES , *MEDICAL cooperation , *MEDICAL research , *PREVENTIVE health services , *RESEARCH ,TUMOR prevention - Abstract
The Cancer Prevention and Control Research Network (CPCRN) is a thematic network dedicated to accelerating the adoption of evidence-based cancer prevention and control practices in communities by advancing dissemination and implementation science. Funded by the Centers for Disease Control and Prevention and National Cancer Institute, CPCRN has operated at two levels: Each participating network center conducts research projects with primarily local partners as well as multicenter collaborative research projects with state and national partners. Through multicenter collaboration, thematic networks leverage the expertise, resources, and partnerships of participating centers to conduct research projects collectively that might not be feasible individually. Although multicenter collaboration is often advocated, it is challenging to promote and assess. Using bibliometric network analysis and other graphical methods, this paper describes CPCRN's multicenter publication progression from 2004 to 2014. Searching PubMed, Scopus, and Web of Science in 2014 identified 249 peer-reviewed CPCRN publications involving two or more centers out of 6,534 total. The research and public health impact of these multicenter collaborative projects initiated by CPCRN during that 10-year period were then examined. CPCRN established numerous workgroups around topics such as: 2-1-1, training and technical assistance, colorectal cancer control, federally qualified health centers, cancer survivorship, and human papillomavirus. This paper discusses the challenges that arise in promoting multicenter collaboration and the strategies that CPCRN uses to address those challenges. The lessons learned should broadly interest those seeking to promote multisite collaboration to address public health problems, such as cancer prevention and control. [ABSTRACT FROM AUTHOR]
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- 2017
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7. Centers for Disease Control and Prevention's Expert Panel on Protective Factors for Youth Violence Perpetration: Background and Overview
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Hall, Jeffrey E., Simon, Thomas R., Mercy, James A., Loeber, Rolf, Farrington, David P., and Lee, Rosalyn D.
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PREVENTIVE medicine , *ETIOLOGY of diseases , *YOUTH violence , *PANEL analysis , *MEDICAL research - Abstract
Abstract: The CDC Expert Panel on Protective Factors for Youth Violence Perpetration was convened to review and advance the status of etiologic and prevention research on direct protective and buffering protective factors for youth violence perpetration. The current paper introduces Phase One of the panel''s work, which focuses on direct protective factors and includes the papers in this supplement to the American Journal of Preventive Medicine. This paper provides the context for the panel''s work, describes its practical and theoretic importance, and summarizes why independently defined direct protective factors and risk factors are important for the advancement of our understanding of youth violence and its prevention. Lastly, this paper briefly describes the organization of the work of the panel as well as the research products that comprise the contents of the supplement. [Copyright &y& Elsevier]
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- 2012
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8. Research Challenges for Electronic Health Records
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Lobach, David F. and Detmer, Don E.
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MEDICAL care , *ONLINE information services , *MEDICAL records , *MEDICAL research - Abstract
Abstract: The availability and use of electronic health records (EHRs) are likely to increase markedly over the next 10 years. This promulgation of EHRs will change dramatically the delivery of healthcare in the United States. Researchers seeking to maximize the impact of EHRs face at least two major and quite different challenges. First, rigorous evaluations of EHR systems are vital but not easily achieved. Second, researchers must determine how to take full advantage of the potential to create and disseminate new knowledge that is possible as a result of the data that are captured by EHRs. This paper reviews critical methodologic issues that need to be considered in the evaluation of EHRs, identifies pivotal policy issues that impact the ability of researchers (and public health professionals) to use the data that will accumulate as a result of EHR diffusion, and recommends actions for those who are interested in changing the landscape of EHR development, research, and implementation. [Copyright &y& Elsevier]
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- 2007
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