eConsent is one of the newest and most exciting technological advancements in clinical trials, with potential to shape the way clinicians and subjects are able to interact on clinical studies, bringing streamlined workflows and higher patient satisfaction to the entire informed consent process.
Subject recruitment and enrollment remain major challenges in clinical trials. Over 40% of clinical trials struggle to meet minimum enrolment goals, leaving many sponsors struggling to conduct trials. In addition, 85% of clinical trials fail to retain enough patients, with the average dropout rate across all clinical trials as high as 30%.
As a follow-up to our 2017 State of eConsent industry report, CRF Health wanted to gather site staff opinions on the impacts the paper-based informed consent process has on participant understanding, recruitment and retention.
This site-specific survey gathered feedback from 105 respondents in roles including study coordinator, CRA, investigator, and researcher. Whether your organization is just starting to consider eConsent or looking to expand adoption, we hope that these survey findings provide insight and context into the perspectives of site staff.
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