Event Location

Attendee Categories

Early Bird - LMIC

Cost

£325.00

Description

Person residing in a low and middle income country, as defined by DAC list (https://www.oecd.org/dac/financing-sustainable-development/development-finance-standards/daclist.htm), at the time of registration. Access to all 5 days of the course.  All course materials will be provided in a large delegate folder, provided to you at the start of the course.  Light refreshments will be provided in the morning before the course begins and for the morning and afternoon breaks.  A buffet lunch will also be provided.  Free parking is available on-site.

Additional Items

Contact

[email protected]

0115 8231600

More Information

The course introduces the key considerations when designing and conducting a randomised clinical trial.

Throughout the five-day course, delegates will learn why clinical trials are necessary, how different kinds of trials are designed and how bias can be minimised, how trials are managed and then analysed, interpreted and reported.

The course will not consider non-randomised trials or other observational designs, or trials evaluating diagnostic tests.  We will primarily focus on large multi-centre trials, considering both drug and complex intervention trials.

 By the end of the course, participants should:

• understand when and why randomised controlled trials are necessary
• understand and evaluate methods to minimise bias in the design and conduct of randomised controlled trials
• be aware of different designs for randomised trials and their use
• be aware what information is required to estimate the size of a trial
• be able to participate in the design of a randomised clinical trial
• understand how an economic evaluation can be embedded into a clinical trial

• understand how using qualitative methodologies can complement a clinical trial
• understand the importance of Patient and Public Involvement (PPI) throughout the lifecycle of a trial
• understand when and which approvals and regulations are needed in clinical trials
• have an understanding of a clinical trial protocol and other trial documentation
• have an understanding of factors to consider when undertaking a multi-centre clinical trial
• be aware of trial safety and requirements for clinical trials involving medicinal products
• have an understanding of risk assessment, data collection and monitoring of trial data
• know how to report and interpret results from a randomised clinical trial

The course will comprise of lectures, workshops and discussion.
 

Who the course is intended for?

The course is intended for anyone seeking an introductory course on randomised controlled trials, and who is likely to be involved in the design, conduct and management, analysis, reporting or review of clinical trials.

 
Course tutors

All sessions on the course will be led by experienced trialists and staff from Nottingham Clinical Trials Unit.

If you are no longer available to attend

You can postpone your place to the next available course. Please note this may be up to 12 months in the future.

If you do not want to postpone your place, you should cancel at your earliest convenience. If you cancel more than 14 calendar days before the start of the course, you are eligible for a full refund for course fees. Refunds after this time are not possible.

Course Cancellations

In the unlikely event that a course has to be cancelled, we will make a decision 4 weeks before the start of the course.  In this instance you will be contacted by email.  Participants will be offered transfer of their course fees to the next available course, which could be up to 12 months in the future, or a full refund.  Our liability is limited to course fees only - we will not refund any travel or accommodation expenses incurred.  We recommend participants have adequate cover to reclaim any travel or accommodation expenses.

For further information please contact [email protected]