Basic Clinical Research Tools

Subject CLRS90010 (2010)

Note: This is an archived Handbook entry from 2010.

Credit Points:

12.50

Level:

9 (Graduate/Postgraduate)

Dates & Locations:

This subject has the following teaching availabilities in 2010:

Semester 1, Hawthorn - Taught on campus.

Pre-teaching Period Start	not applicable
Teaching Period	not applicable
Assessment Period End	not applicable
Last date to Self-Enrol	not applicable
Census Date	not applicable
Last date to Withdraw without fail	not applicable

Intensive

Timetable can be viewed here. For information about these dates, click here.

Time Commitment:

Contact Hours: 24 hours of lectures/seminars/workshops
Total Time Commitment: Students should expect to undertake a minimum of 120 hours lectures, research, reading, writing etc to complete this subject successfully.

Prerequisites:

nil

Corequisites:

nil

Recommended Background Knowledge:

nil

Non Allowed Subjects:

nil

Core Participation Requirements:

For the purposes of considering requests for Reasonable Adjustments under the Disability Standards for Education (Cwth 2005), and Students Experiencing Academic Disadvantage Policy, academic requirements for this subject are articulated in the Subject Description, Subject Objectives, Generic Skills and Assessment Requirements of this entry.
The University is dedicated to provide support to those with special requirements. Further details on the disability support scheme can be found at the Disability Liaison Unit website: http://www.services.unimelb.edu.au/disability/

Contact

Melbourne Consulting and Custom Programs

Level 3, 442 Auburn Rd

Hawthorn VIC 3122

Phone: 9810 3300

Email: clinicalresearch@mccp.unimelb.edu.au

Subject Overview:	Topics covered include: Basic descriptive data Probability and inference Analysis of two-way tables Differences of Means Simple correlation Case-series, cross-sectional, cohort, case-control studies and Randomised Clinical Trials (RCTs). Measurement of exposure Measurement of response Bias, random error and individual variation (including response variation) Sample size and power
Objectives:	Students who successfully complete this subject will be able to:  Understand the basic principles in Epidemiology and Biostatistics.  Understand the strengths and weaknesses of different study designs  Understand basic principles of epidemiological and clinical research  Be familiar with terms used in the literature  Understand statistical reasoning, including inference and the need for power and appropriate samples  Perform basic statistical processes  Understand the role, strengths and weaknesses of different study designs
Assessment:	A series of epidemiological and biostatistical exercises equivalent to 2,000 words (50%), and a review of segments of journal articles of 2,000 words (50%).
Prescribed Texts:	nil
Recommended Texts:	Students will be provided with articles and references that support the teaching program as part of their course materials.
Breadth Options:	This subject is not available as a breadth subject.
Fees Information:	Subject EFTSL, Level, Discipline & Census Date
Generic Skills:	Students who successfully complete this subject will be able to: Understand the basic principles in Epidemiology and Biostatistics. Understand the strengths and weaknesses of different study designs Understand basic principles of epidemiological and clinical research Be familiar with terms used in the literature Understand statistical reasoning, including inference and the need for power and appropriate samples Perform basic statistical processes Understand the role, strengths and weaknesses of different study designs
Links to further information:	http://www.mccp.unimelb.edu.au/courses/award-courses/graduate-certificate/clinical-research
Related Course(s):	Graduate Certificate in Clinical Research Graduate Diploma in Clinical Research Master of Clinical Research Professional Certificate in Clinical Research

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