Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Marjorie J. Good"'
Autor:
Colleen Shannon, Grant D. Huang, Marjorie J. Good, Mary Brophy, Andrea Denicoff, Sara J. Schiller, Sheila A. Prindiville
Publikováno v:
Seminars in Oncology. 46:308-313
Cancer clinical trials represent an important option for patients with a diagnosis of cancer and the clinician-investigators involved in their care who seek options for their disease. For all who are impacted by cancer, these studies offer opportunit
Autor:
Kathleen Castro, Shanda Finnigan, Diane St. Germain, Andrea Denicoff, Linda Parreco, Marjorie J. Good
Publikováno v:
Seminars in oncology nursing. 36(2)
Objectives To describe the evolution and structure of the National Cancer Institute clinical trials programs, their notable accomplishments, nurses’ roles in these accomplishments, and the essential role of nursing today and in the future. Data Sou
Autor:
Matthew J. Boron, Bhanu Ramineni, Marjorie J. Good, Michael Montello, Jeffrey A. Moscow, Grace Mishkin, James H. Doroshow, Margaret M. Mooney, Rodney Howells, Worta McCaskill-Stevens, Gary L. Smith, Martha Kruhm, S. Percy Ivy, Andrea Denicoff, Shanda Finnigan, Sharon Hampp
Publikováno v:
Journal of Clinical Oncology. 39:1562-1562
1562 Background: The National Cancer Institute supports several national trial networks which responded rapidly to the COVID-19 pandemic to overcome operational barriers to clinical cancer research. The National Clinical Trials Network (NCTN) focuses
Autor:
Iman K. Martin, Worta McCaskill-Stevens, Marjorie J. Good, Mary Shaw-Ridley, Brenda A. Adjei, Dudith Pierre-Victor, Bruce D. Rapkin, Bernard W. Parker, Diane St. Germain
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 29:D079-D079
Background Cancer frequently occurs with other chronic diseases, and this poses serious care coordination challenges during patients’ active cancer treatment (ACT) and contributes to disparities in health outcomes. There is limited research address
Autor:
Diane St. Germain, Marjorie J. Good
There are essential elements that need to be in place to conduct a clinical trial successfully. First is a knowledgeable, adequately staffed research team well versed in the conduct of clinical research. Second, a clearly written protocol document th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adc608bbafaea4ff51d3f21372bff080
https://doi.org/10.1016/b978-0-12-849905-4.00030-7
https://doi.org/10.1016/b978-0-12-849905-4.00030-7
Autor:
Paul S. Albert, Elizabeth A. Bartrum, Karen E. Berliner, Juliana Blome, Enriqueta Bond, Valerie H. Bonham, Craig B. Borkowf, John T. Burklow, Robert M. Califf, Leighton Chan, Sue Cheng, James J. Cimino, Janine Clayton, Patricia S. Coffey, Melissa C. Colbert, Josh A. Duberman, Michelle Feige, Cheryl A. Fisher, Molly M. Flannery, Maryrose Franko, Bradley D. Freeman, Elaine K. Gallin, John I. Gallin, Naomi L. Gerber, Bruce Goldstein, Marjorie J. Good, Michael M. Gottesman, Christine Grady, David K. Henderson, Nicholas C. Ide, Jonathan P. Jarow, Laura Lee Johnson, Barbara I. Karp, Phyllis Klein, Laura M. Lee, Juan J.L. Lertora, Diane M. Maloney, Patrick McGarey, Amy E. McKee, Jon W. McKeeby, Theresa Mullin, Charles Natanson, Lynnette Nieman, Robert B. Nussenblatt, Frederick P. Ognibene, Christopher O. Olopade, Olufunmilayo I. Olopade, Valerie L. Prenger, Jillian K. Price, Michael A. Proschan, Jerry Sachs, Joseph A. Sclafani, Joe V. Selby, Pamela A. Shaw, Kelly S. Sherman, Pamela C. Sieving, Amy P.N. Skubitz, Jean R. Slutsky, Julia Slutsman, Diane C. St Germain, Catherine M. Stoney, Stephen E. Straus, Elyse I. Summers, Junfeng Sun, Michelle Tagle, Tony Tse, Konstantina M. Vanevski, Paul G. Wakim, Gwenyth R. Wallen, Evelyn P. Whitlock, Rebecca J. Williams, Deborah A. Zarin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cbfd98a0c929e79f2d1fe59daca5ed0
https://doi.org/10.1016/b978-0-12-849905-4.01002-9
https://doi.org/10.1016/b978-0-12-849905-4.01002-9
Autor:
Patricia Hurley, Marjorie J. Good, Kelly Willenberg, Dax Kurbegov, Casey Dawson, Andrea Denicoff, Connie M. Szczepanek
Publikováno v:
Journal of oncology practice. 13(6)
Purpose: Clinical trial billing compliance is a challenge that is faced by overburdened clinical trials sites. The requirements place institutions and research sites at increased potential for financial risk. To reduce their risk, sites develop a cov
Autor:
Mona N. Fouad, Marjorie J. Good, William J. Hicks, Robert L. Comis, Stephen S. Grubbs, Steven Joffe, Worta McCaskill-Stevens, Steven N. Wolff, Rebecca A. Enos, Afshin Dowlati, Michelle E. Duff, Ellen S. Richmond, Kevin P. Weinfurt, Michael A. Bookman, Patrick J. Loehrer, Robin T. Zon, Neal J. Meropol, Andrea Denicoff, Terrance L. Albrecht, Alan P. Lyss, Margo Michaels, Jean G. Ford, Lidia Schapira, Debra Wujcik, Derek Raghavan, David M. Dilts, Suanna S. Bruinooge, Peggy Devine
Publikováno v:
Journal of Oncology Practice. 9:267-276
Many challenges to clinical trial accrual exist, resulting in studies with inadequate enrollment and potentially delaying answers to important scientific and clinical questions.The National Cancer Institute (NCI) and the American Society of Clinical
Publikováno v:
Contemporary Clinical Trials. 34:320-325
Determining the factors that lead to successful enrollment of patients in cancer control clinical trials is essential as cancer patients are often burdened with side effects such as pain, nausea, and fatigue. One promising intervention for increasing
Autor:
Rogerio Lilenbaum, Kaitlin M. Woo, Connie M. Szczepanek, Patricia Hurley, Mithat Gonen, Nicholas Robert, Marjorie J. Good, Alan Lyss, Teresa L. Stewart
Publikováno v:
Journal of oncology practice. 12(5)
Purpose: Clinical research program managers are regularly faced with the quandary of determining how much of a workload research staff members can manage while they balance clinical practice and still achieve clinical trial accrual goals, maintain da