EPI 205 Winter 2019 (1.5 units)
The objectives of this course are to provide a detailed understanding of experimental study design options; methods of randomization; blinding; developing interventions and comparators; measuring outcomes and adverse effects; follow-up; compliance and postrandomization problems.
Designing Clinical Research (EPI 202). Exceptions to this prerequisite may be made with the consent of the Course Director, space permitting.
Course content will be delivered through lectures and small group sections.
All course materials and handouts will be posted on the course's online syllabus.
Designing Clinical Research by Stephen B. Hulley, et al. Lippincott Williams & Wilkins. 4th Edition. 2013.
Books may be purchase either through the publisher or a variety of commercial venues (e.g., Amazon.com).
Grades will be based on total points achieved on homework (~25%), protocol development and critiquing (~50%), and the final exam (~25%). Late assignments are not accepted.
Homework is due by 5 PM on the Monday following the lecture when the homework is assigned. Homework assignments will be discussed in the Small Group Sections.
Protocol Assignment: Email a copy of your cumulative protocol to your section leader by noon the Monday before each Small Group Section.
Students not in full-year TICR Programs who satisfactorily pass all course requirements will, upon request, receive a Certificate of Course Completion.
This course is sponsored by the Training in Clinical Research (TICR) Program, and space is limited. Preference is given to UCSF-affiliated personnel. We regret that auditing is not permitted.
To apply for this course, please fill out and submit the application below. Please see our fees page for cost information. The deadline for application is December 21, 2018. Only one application needs to be completed for all courses desired during the quarter.
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