Improving the guidelines for Informed Consent

i-CONSENT, funded by the European Union H2020 programme, aims to improve the information that patients receive from clinical studies. Within the project, a series of guidelines to improve Informed Consent process will be created, including vulnerable populations, under a gender perspective and relying on ICT tools.

The Project

F2F Meeting in Rome: Finalising the guidelines

Nov 7, 2019

The i-CONSENT Consortium met in Rome to give the final touches to the project's guidelines Consortium representatives sat the past November 4-6 around the table to give the final push the project's product. The i-CONSENT guidelines, with an innovative format, are...

i-CONSENT at the 25th Congress of Spanish Association of Bioethics

Oct 31, 2019

i-CONSENT participated the past October 25-26th in the 25th National Congress of the Spanish Association of Bioethics and Medical Ethics (AEBI ) held in Valencia. Topics such as human dignity, the ethics of the end of life, the ethics in assisted reproduction were...

i-CONSENT with Health Literacy Month 2019

Oct 28, 2019

6 reasons to participate in clinical trials October is #HealthLiteracyMonth and #iCONSENT is joining the celebration! For this purpose we explored 6 reasons why someone should participate in a #clinicaltrial. Before a treatment is commercialized it must undergo a...

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H2020 project aimed to improve #informedconsent by focusing on gender, age and vulnerable populations to promote patient autonomy and empowerment through TIC.

i-CONSENT @ICONSENTEU·

12 Nov

#DesignThinking | We are in Elche today holding a Design Thinking session with pregnant women and midwives, working on the inclusion of #gender perspective in our guidelines. Very interesting points where raised!
🗯️ #iCONSENT #H2020 #ResearchEU
🔗 http://www.i-consentproject.eu

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i-CONSENT in Numbers

From 2017 to 2020

Partners

Million EU Funding

Countries

Years Duration

Multimedia

i-CONSENT falls under the ‘Science with and for Society’ (SWAFS) programme, which means that finding ways of connecting science to society is one of its main goals. Well aware of this, i-CONSENT is committed to citizens’ health literacy not only as a solution to make science more attractive to them but also as a way of empowering them leading to a true autonomy and self-government when deciding to participate in health-related studies. This section will offer visitors and stakeholders information on the project, in particular, and knowledge on clinical trials, research and ethics, in general.