“Welcome to
the i-CONSENT project.

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


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

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

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

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

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

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

This project has received funding from the European Union’s Horizon 2020 research and innovation programme under Grant Agreement No 741856