Mini-course – Information & consent in trials

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Introduction

This EUPATI Mini-course starter kit is designed for patient involvement in product information, informed consent and patient information to trial participants.

EUPATI Mini-course starter kits have been derived from content found in the EUPATI toolbox and EUPATI Patient Expert Training Course. The starter kits are thought to address roles that patients play in medicines development for example those shown in the figure below.

The starter kits provide you with links to relevant background reading in the toolbox and associated PowerPoint slide decks and media in order to prepare a single or multi-day training on the subject. Each of the starter kits contains a selection of PPT slides which you may use to educate patients/advocates about the “basics” in that area, e.g. in a two-hour to one-day seminar.

The starter kits are based on existing content from the EUPATI Toolbox, plus additional links to add-on Toolbox material. None of the “starter kits” are “ready-made course” modules – they are a ready-to-reuse resource for an experienced trainer to prepare and execute a course. You will need to edit them and put them into context.

Before you begin please download and review the ‘Manual for Trainers’.

Product information, informed consent and patient information to trial participants

This starter kit provides background reading, slides, a video, and quizzes to create training for patients who intend to become involved in product information, informed consent and patient information to trial participants.

Core reading

Risk communication in medicines

Information on medicinal products

Participants rights responsibilities organisations

Recording and reporting of clinical trial results

Clinical study results publication and application

Optional

There is no optional content in the setting research priorities starter kit.

Presentations

Quizzes

Quizzes will be provided for each presentation in the future on:

Risk communication in medicines

Information on medicinal products

Participants rights responsibilities organisations

Recording and reporting of clinical trial results

Clinical study results publication and application

Videos

Informed consent for vulnerable populations (Webinar)

Terms of use - Creative Commons

Remember that all educational content provided by EUPATI is released under a Creative Commons License, which also applies to all derivatives of it! You can read more about the use of EUPATI content on the Creative Commons page.

Use of the EUPATI logo

The EUPATI logo is protected by trademark and owned by the European Patients Forum.

Except for the limited purpose of indicating that work is created or licensed by EUPATI (European Patients Academy for Therapeutic Innovation), or collaboration with EUPATI, the European Patients Forum (EPF) does not authorise the use, by any party, of the trademark "EUPATI" or any related trademark or logo of EUPATI without the prior written consent of EPF. Any permitted use will be in compliance with EUPATI's then-current trademark usage guidelines, as may be published on its website or otherwise made available upon request from time to time.

A2-SK-product-information-informed-consent-patient-information-to-trial-participants-V1.0

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