Clinical Trials – Do patients understand enough to give truly informed consent?
Recent research undertaken by luto for the University of Leeds showed that participants were unable to find or understand key information in clinical trial patient information sheets (PIS).
Working with a representative participant cohort, luto can identify problems with information sheets and consent forms, then using the best practice in information design, refine and test the revised copy.
Working with a representative participant cohort, luto can identify problems with information sheets and consent forms, then using the best practice in information design, refine and test the revised copy.
This allows our clients to apply for research ethics approval demonstrating that the PIS has been tested and that potential trial participants can understand the key points. It also reduces liability as far as trial insurers are concerned, often reducing insurance premiums.
