Un progetto per il miglioramento del processo del consenso informato
i-CONSENT, finanziato dal programma Horizon 2020 dell’Unione Europea, ha lo scopo di migliorare il modo in cui i pazienti ricevono le informazioni dagli studi clinici. All’interno del progetto, verranno create una serie di linee guida per il miglioramento del processo del consenso informato, con particolare riguardo ai gruppi vulnerabili, secondo una prospettiva di genere e basandosi sulle tecnologie ICT.
Has paper-based Informed Consent era come to an end?
eConsent is consolidating itself as benchmark in the development of health-related studies Although there has been a change since those everlasting 15-20 page long Informed Consent (IC) documents, when participating in clinical studies potential participants still...
leggi tutto5 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...
leggi tuttoi-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...
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@ICONSENTEU
What are the 4 pillars of medical #ethics? @BiobancoLaFe explains them here 👇
🗯#iCONSENT #H2020 #ResearchEU
🔗https://t.co/S45Imy8ePp
👩🔬👩⚖️👥 Hoy recordamos los 4️⃣ #PrincipiosBioética (Tom Beauchamp&James Franklin Childress, 1979):
👁️🗨️#Autonomía: capacidad de decisión.
🤲#Beneficiencia: beneficio > riesgo.
❌#NoMaleficencia: no hacer daño.
⚖️#Justicia: igualdad oportunidades.
@FECYT_Ciencia @WHO @aecc_es