JSM Activity #CE2003_20CThis is the preliminary program for the 2003 Joint Statistical Meetings in San Francisco, California. Currently included in this program is the "technical" program, schedule of invited, topic contributed, regular contributed and poster sessions; Continuing Education courses (August 2-5, 2003); and Committee and Business Meetings. This on-line program will be updated frequently to reflect the most current revisions. To View the Program: You may choose to view all activities of the program or just parts of it at any one time. All activities are arranged by date and time. |
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Legend: = Applied Session,
= Theme Session,
= Presenter Hotels: H = Hilton San Francisco, R = Reniassance Parc Hotel 55, N = Nikko San Francisco |
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CE2003_20C | Tue, 8/5/03, 8:15 AM - 4:15 PM | N-Carmel Room I |
Design Monitoring, and Analysis of Group Sequential Clinical Trials - Continuing Ed | ||
ASA, Biometrics Section | ||
Instructor(s): Scott S. Emerson, University of Washington | ||
Increasingly, clinical trials are conducted using group sequential methods in order to address the ethical and efficiency issues that arise when performing experiments with human volunteers. The design, conduct, and analysis of a sequential clinical trial is necessarily more involved than that for a clinical trial in which the data would only be analyzed at the end of the study. In this one day short course I present the additional issues that must be considered when designing, monitoring, and reporting the results of a group sequential trial. The morning session will be a qualitative presentation of the issues that arise in the conduct of clinical trials, especially as it pertains to the monitoring of such trials. The intended audience is researchers who want to understand the basic principles that should be used to assess whether the monitoring plan for a particular clinical trial is appropriate. No knowledge of statistics is presumed.The afternoon session will be a more quantitative presentation of the statistical design of clinical trials. The intended audience is researchers active in designing clinical trials or in evaluating the statistical operating characteristics of such designs. Knowledge of hypothesis testing and clinical trial design for comparing means or binomial proportions in nonsequential studies is presumed. Fees: M- $325 ($430 after July 18), NM- $415 ($520 after July 18), SM- $200 ($325 after July 18) | ||
JSM 2003
For information, contact meetings@amstat.org
or phone (703) 684-1221. If you have questions about the Continuing Education program,
please contact the Education Department. |