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pro vyhledávání: '"Kimberley N. Chapman"'
Autor:
Stefan V. Goldberg, Emily J. Hecker, Patricia A. Bessler, Kimberley N Chapman Hedges, Antonio Moreno-Martinez, Jussi J. Saukkonen, Amy Kerrigan, Bert Arevalo, Nigel A. Scott, Carol Dukes Hamilton, Lorna Bozeman, Andrey S. Borisov
Publikováno v:
Clin Trials
Background/aimsEfficient recruitment of eligible participants, optimizing time and sample size, is a crucial component in conducting a successful clinical trial. Inefficient participant recruitment can impede study progress, consume staff time and re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e5ad08cd16e3ca9d9e1eabd5b30b169
https://doi.org/10.1177/1740774519885380
https://doi.org/10.1177/1740774519885380
Autor:
Kuo Wei Chiu, Kathleen Robergeau-Hunt, Pamela Fedrick, Anne E. Purfield, Mascha Elskamp, Yan Yuan, Nicole E Brown, Kim Narunsky, William C. Whitworth, Kimberley N Chapman Hedges, Ekaterina V. Kurbatova, Melissa Fagley, Erin Sizemore, Melissa Engle, Joanita Nassali, Cynthia Allen-Blige, Kumar Batra, Jessica N Ricaldi, Howard Davis, Kia E Bryant, Ha Phan, Mimi Phan
Publikováno v:
Contemp Clin Trials
Introduction With the growing use of online study management systems and rapid availability of data, timely data review and quality assessments are necessary to ensure proper clinical trial implementation. In this report we describe central monitorin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffebd0194dfb50408522d91d1abf0c15
https://pubmed.ncbi.nlm.nih.gov/33713841
https://pubmed.ncbi.nlm.nih.gov/33713841
Akademický článek
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Autor:
Hedges, Kimberley N Chapman, Borisov, Andrey S, Saukkonen, Jussi J, Scott, Nigel A, Hecker, Emily J, Bozeman, Lorna, Hamilton, Carol Dukes, Kerrigan, Amy, Bessler, Patricia, Moreno-Martinez, Antonio, Arevalo, Bert, Goldberg, Stefan V
Supplemental material, TBTC_S26_Nonparticipation_ClinicalTrials_Online_Supplement for Nonparticipation reasons in a randomized international trial of a new latent tuberculosis infection regimen by Kimberley N Chapman Hedges, Andrey S Borisov, Jussi J
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f11b9dc068e7c39fd7229291dd66307
Autor:
Kimberley N. Chapman, Joseph G. Nakibali, Peter Breese, Stefan V. Goldberg, Eric Pevzner, Robin Shrestha-Kuwahara, Dorcas Lamunu, Joan M. Mangan
Publikováno v:
AJOB empirical bioethics. 6(4)
Ethical principles obligate researchers to maximize study participants' comprehension during the informed consent process for clinical trials. A pilot evaluation of the consent process was conducted during an international clinical trial of treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eb8e87da2a5ce656a90e731e4ca1066
https://pubmed.ncbi.nlm.nih.gov/28317002
https://pubmed.ncbi.nlm.nih.gov/28317002