Postgraduate Course: Introduction to Clinical Trials (MCLM11002)
Course Outline
School | School of Molecular, Genetic and Population Health Sciences |
College | College of Medicine and Veterinary Medicine |
Credit level (Normal year taken) | SCQF Level 11 (Postgraduate) |
Course type | Online Distance Learning |
Availability | Not available to visiting students |
SCQF Credits | 20 |
ECTS Credits | 10 |
Summary | This compulsory course forms the foundation for many of the subsequent courses on the MSc in Clinical Trials programme. A detailed understanding of the clinical trial process is essential for all members of the trial team.
Course participants will learn how research hypotheses are formulated and tested and will follow the process from initial concept through to the development of a clinical trial protocol and then on to the execution of the study and ultimately the dissemination of research findings.
The focus of the course will be threefold:
¿ The design of clinical trials
¿ The principles of their analysis
¿ The interpretation of their findings
Course participants will learn about different design elements of clinical trials. The concepts of randomisation, blinding, bias, internal and external validity, the definition of study endpoints and the choice of appropriate outcome measures will be thoroughly explored as will the need for the selection of appropriate populations and power calculations.
Protocol design will be examined in detail and use will be made of clinical trial case studies including those testing both pharmacologic and non-pharmacologic interventions.
Successful participants will gain a firm understanding and practical knowledge of the key elements and principles of clinical trial design, delivery and analysis.
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Course description |
Not entered
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Entry Requirements (not applicable to Visiting Students)
Pre-requisites |
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Co-requisites | |
Prohibited Combinations | |
Other requirements | None |
Course Delivery Information
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Academic year 2014/15, Not available to visiting students (SS1)
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Quota: None |
Course Start |
Semester 1 |
Timetable |
Timetable |
Learning and Teaching activities (Further Info) |
Total Hours:
200
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Seminar/Tutorial Hours 5,
Online Activities 100,
Feedback/Feedforward Hours 40,
Formative Assessment Hours 12,
Summative Assessment Hours 10,
Revision Session Hours 8,
Programme Level Learning and Teaching Hours 4,
Directed Learning and Independent Learning Hours
21 )
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Assessment (Further Info) |
Written Exam
0 %,
Coursework
100 %,
Practical Exam
0 %
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Additional Information (Assessment) |
5000 word essay - 50%
Discussion Board - 25%
MCQ - 25% |
Feedback |
Not entered |
No Exam Information |
Learning Outcomes
On completion of this course, the student will be able to:
- Critically assess the factors that contribute to suitable trial design for a research question including selection of appropriate endpoints, choice of sample size, data analysis, presentation of results and implementation in routine clinical practice
- Engage and contribute to current and emerging debate around clinical trial transparency, registration and disclosure
- Contribute to the design, authoring and evaluation of a clinical trials protocol; critically discuss the challenges of clinical trial delivery including study design, trial set up, recruitment, follow up and data collection
- Apply the principles of data analysis, dissemination of results and implementation of key findings
- Critically appraise the methods by which procedural and epidemiological data underpin the development of clinical trials
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Additional Information
Graduate Attributes and Skills |
Not entered |
Keywords | Clinical research, Trial management |
Contacts
Course organiser | Miss Michelle Evans
Tel: 0131 537 3326
Email: michelle.evans@ed.ac.uk |
Course secretary | Mrs Danielle Marlow
Tel: 0131 537 3798
Email: Danielle.Wilson@ed.ac.uk |
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© Copyright 2014 The University of Edinburgh - 12 January 2015 4:23 am
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