E-Consent

Purpose

E-Consent is a multipurpose, scalable, electronic informed consent system that can be used in a multitude of settings. The platform allows research staff to easily upload multimedia information about a research protocol together with an approved informed consent. These materials are then delivered to potential study participants electronically, in an easy-to-understand and user-friendly way. The system is compatible with a wide range of devices and display sizes, including tablets, mobile devices, laptops, desktops, and others. Further details are available at https://www.ncbi.nlm.nih.gov/pubmed/31349301.

E-Consent has been developed in collaboration with the Mount Sinai IRB to ensure regulatory compliance: IRB-19-02049 Assessment of Multipurpose Scalable Electronic Informed Consent Platform.

Office

Office of Chief Research Informatics Officer (CRIO)

Access

If you would like to explore and/or use this offering for your research projects, please open a CRIO / e-Consent ticket at http://osticket.mssm.edu/support/. Irena Parvanova, PhD, will respond.

Please be prepared to provide the following documentations to ensure IRB compliance.

• Full IRB-approved protocol
• Letter of approval

If you have additional questions you may email Irena.Parvanova@mountsinai.org.

Cost

Free for all clinical research projects.

Consent Video

Dashboard Video

Participant Video