Recruiting And Retaining Patients With eConsent

Source: CRF Health

The informed consent process intends to ensure trial participants understand the risks and benefits of joining your trial, but a poor experience leads to low recruitment rates and costly drop-outs. Electronic Informed Consent (eConsent) improves recruitment and retention of participants by developing better comprehension of consent materials and improving engagement for the full duration of your study. In this short video, industry expert Sandra "Sam" Sather, reviews the ways that eConsent supports and adds value to the recruitment process.