5 frequently asked questions (FAQs) on Informed Consent
Many doubts arise when taking part on a clinical study. More than a mere disclaimer, informed consent processes exist to tackle them. Based on frequent Google searches, i-CONSENT has selected 5 frequently asked questions on Informed Consent that you might have come...
i-CONSENT involves children in the project through Design Thinking
i-CONSENT team organised last week a workshop with children to assess their knowledge on clinical studies and develop strategies to better communicate with them Participation of children in clinical studies is essential but still minoritary. How to communicate with...
Gaps and challenges to the Informed Consent Process by i-CONSENT
It is generally agreed that informed consent is a process whose effectiveness is a factor of a few core criteria. These criteria are typically held to include concepts such as disclosure, understanding, capacity, and voluntariness. Though guidelines differ somewhat in...
i-CONSENT brings project conclusions before the Spanish Research Ethic Committees
The VI ANCEI Congress was celebrated on May 30 and 31 in Tarragona For second year in a row, the i-CONSENT project participated in the ANCEI Congress in its VI edition, taking the first project results before the Spanish Research Ethic Committees. i-CONSENT...
Next steps for i-CONSENT
From WP2 and WP3 to the elaboration of the guidelines With approximately one year of project left, i-CONSENT is starting to translate the findings into a set of guidelines to improve Informed Consent. The conclusions of i-CONSENT WP1 (Work package 1, A...i-CONSENTFollow
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