Postgraduate Course: Clinical Trials (PUHR11021)
Course Outline
| School | School of Molecular, Genetic and Population Health Sciences |
College | College of Medicine and Veterinary Medicine |
| Course type | Standard |
Availability | Available to all students |
| Credit level (Normal year taken) | SCQF Level 11 (Postgraduate) |
Credits | 10 |
| Home subject area | Public Health Research |
Other subject area | None |
| Course website |
http://www.chs.med.ed.ac.uk/education/mph/ |
Taught in Gaelic? | No |
| Course description | Design of clinical trials, principles of analysis, and interpretation of findings. |
Entry Requirements (not applicable to Visiting Students)
| Pre-requisites |
|
Co-requisites | |
| Prohibited Combinations | |
Other requirements | None |
| Additional Costs | None |
Information for Visiting Students
| Pre-requisites | None |
| Displayed in Visiting Students Prospectus? | Yes |
Course Delivery Information
|
| Delivery period: 2014/15 Semester 2, Available to all students (SV1)
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Learn enabled: Yes |
Quota: None |
|
Web Timetable |
Web Timetable |
| Course Start Date |
12/01/2015 |
| Breakdown of Learning and Teaching activities (Further Info) |
Total Hours:
100
(
Lecture Hours 10,
Seminar/Tutorial Hours 2,
Supervised Practical/Workshop/Studio Hours 4,
Other Study Hours 2,
Programme Level Learning and Teaching Hours 2,
Directed Learning and Independent Learning Hours
80 )
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| Additional Notes |
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| Breakdown of Assessment Methods (Further Info) |
Written Exam
0 %,
Coursework
100 %,
Practical Exam
0 %
|
| No Exam Information |
Summary of Intended Learning Outcomes
On completion of the course, the student will be able to:
&·Understand the role of the randomised controlled trial in a range of areas of application.
&·Identify appropriate populations for different types of analysis.
&·Understand the principles of analysis.
&·Contribute to the design of clinical trial protocols.
Areas to be covered include:
&·Basics of clinical trial design
&·Randomisation, avoidance of bias, ethical issues
&·Types of trial design
&·Parallel groups, cross-over trials, sequential methods
&·Sample size
&·Explanatory vs pragmatic trials
&·Regulatory/organisational aspects
&·Analysis of parallel group studies
&·Cross-over trials design and analysis aspects,
&·Two period trials, multi-period trials N-of-1 trials
&·Trials for equivalence
&·Use of baseline values
&·Interpretation of results multiple testing, subgroup analysis published papers
&·Introduction to unusual and advanced methods of design and analysis |
Assessment Information
| Design of a clinical trial protocol |
Special Arrangements
| None |
Additional Information
| Academic description |
Not entered |
| Syllabus |
Not entered |
| Transferable skills |
Not entered |
| Reading list |
Not entered |
| Study Abroad |
Not entered |
| Study Pattern |
Not entered |
| Keywords | Not entered |
Contacts
| Course organiser | Mrs Gillian Mchugh
Tel:
Email: |
Course secretary | Mr Stuart Mallen
Tel: (0131 6)50 3227
Email: |
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