“Welcome to
the i-CONSENT project.

PROJECT AIMS:

Improve information received by participants involved in clinical research.

Create innovative, personalised Informed Consent processes.

Consider gender, age and vulnerable population groups, using both digital and non-digital tools for presenting information.

The main objective of ‘i-CONSENT’ is

Develop better guidelines for Informed Consent documents

1

We aim to make Informed Consent documents more understandable, and participation in research easier, thereby improving patient information, decision-making and autonomy.
2

The materials you will see here have been created following these guidelines with the contribution of other people like you.
3

By taking part in this study, you can help us further improve our i-CONSENT guidelines.
4

This way, we will be able to create improved research projects, in which patient and volunteer participation will be better and safer.
5

We will be using both digital and non-digital tools to present all the necessary information.
6

This new approach will improve participant information, decision-making and autonomy, allowing them to feel safer if they decide to participate in clinical research.

Thank you

for agreeing to take part in this project!

If you are between 9 and 14 years old

Youth Group

If you are expecting

Pregnant Women’s Group

If you are over 18 years old

Adult Group

i-consentproject.eu
@ICONSENTEU
iconsent.project@gmail.com
This project has received funding from the European Union’s Horizon 2020 research and innovation programme under Grant Agreement No 741856