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Certificate On Campus

Successfully Incorporating Patient-Reported Outcomes (PROs) in Clinical Trials University of Birmingham

Highlights
Tuition fee
295 GBP / full
295 GBP / full
Unknown
Tuition fee
295 GBP / full
295 GBP / full
Unknown
Duration
2 days
Duration
2 days
Apply date
Unknown
Unknown
Apply date
Unknown
Unknown
Start date
Unknown
Start date
Unknown
Campus location
Birmingham, United Kingdom
Campus location
Birmingham, United Kingdom
Taught in
English
Taught in
English

About

The Successfully Incorporating Patient-Reported Outcomes (PROs) in Clinical Trials course from the University of Birmingham will provide a detailed understanding of the importance of PROs in clinical trials and best practices for their selection and successful incorporation into a trial.

Overview

Outcomes assessment is a fundamental aspect of clinical trial design and implementation. 

Patient reported outcomes (PROs) provide unique information on the impact of a medical condition and its treatment from the patient’s perspective and are increasingly recognized by regulators, clinicians, and patients as valuable tools to collect patient-centred data.

PROs should be included as primary or secondary outcomes in clinical trials to ensure the impact of a trial intervention is comprehensively assessed.

Key facts

The Successfully Incorporating Patient-Reported Outcomes (PROs) in Clinical Trials course from the University of Birmingham  will also consider the capture of PROs, their analysis and reporting and how their impact on clinical practice can be maximised.

Programme Structure

Learning outcomes:
  • Identify the different types of Patient-Reported Outcomes (PRO) and when to use them in clinical trials
  • Describe approaches to selecting an appropriate PRO measure for a study
  • Recognise and describe PRO-specific components that should be included in a trial protocol using the SPIRIT-PRO Extension
  • Describe approaches to minimising missing data and enhancing data quality
  • Describe the challenges and potential management strategies for PRO Alerts
  • Recognise basic methods of PRO analysis
  • Critique the reporting of a trial using the CONSORT-PRO extension
  • Evaluate ways to maximise the impact of PRO trial data to inform clinical practice and health-policy

Key information

Duration

  • Full-time
    • 2 days

Start dates & application deadlines

Language

English

Delivered

On Campus

Campus Location

  • Birmingham, United Kingdom

What students do after studying

Join for free or log in to access our complete career info list.

Academic requirements

We are not aware of any specific GRE, GMAT or GPA grading score requirements for this programme.

English requirements

We are not aware of any English requirements for this programme.

Other requirements

General requirements

  • This course is aimed at Chief and Principal Investigators, trial managers, clinical researchers, research nurses, data managers, study co-ordinators and academics working within clinical trials. 

Tuition Fees

Tuition fees are shown in and the most likely applicable fee is shown based on your nationality.
  • International

    Non-residents
    295 GBP / full
    295 GBP / full
  • Domestic

    Citizens or residents
    295 GBP / full
    295 GBP / full

Living costs

Birmingham

United Kingdom
765 - 1134 GBP / month

The living costs include the total expenses per month, covering accommodation, public transportation, utilities (electricity, internet), books and groceries.

Funding

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Successfully Incorporating Patient-Reported Outcomes (PROs) in Clinical Trials
University of Birmingham
Successfully Incorporating Patient-Reported Outcomes (PROs) in Clinical Trials
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University of Birmingham

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