H01 PIS Workshop How To Design Clear & Accessible Patient Information Sheets 080725Info Location Attendee Categories Contact More Info Event Information
DescriptionPatient Information Sheets (PIS) are a key document for potential participants to make an informed decision about whether to take part in a clinical study. While there is clear guidance from the Health Research Authority (HRA) on content and regulatory requirements, PIS are customised for each clinical trial and the specific patient population. Choosing the right language and format for patient facing materials for research studies and clinical trials still greatly varies and depends on the skills and experience of the team putting them together.
Course tutors: Linda Von Neree, Patient and Public Involvement and Engagement (PPIE) Lead, BRTU PPI.
Event Location
Attendee CategoriesAttendees From Non-Profit Organisations.
Additional ItemsContactFor all queries in regards to this Course please contact the following :-
PLEASE ONLY CONTACT THE ONLINE STORE DIRECTLY IF YOU ARE EXPERIENCING PROBLEMS WITH YOUR DEBIT/CREDIT CARD PAYMENT, FOR ALL OTHER QUERIES RELATING TO THIS COURSE, INCLUDING CANCELLATIONS THESE SHOULD BE DIRECTED TO THE CONTACT DETAILS ABOVE. More InformationIn this workshop attendees will gain useful insights on how to work on the format, language and delivery of the PIS thanks to the participation of patient representatives with experience in clinical trials of different phases and with different clinical interventions. The session includes an initial overview of the HRA guidance on the PIS design, an introduction to writing in plain English and a patient’s perspective in providing consent to a clinical study, followed by group work where research staff will go into virtual breakout rooms with Patient and Public representatives to review together a PIS that will be provided to the attendees a week prior to the course. Most importantly, at the end of the course, participants will be provided with a “PIS Checklist”: a memorandum of the considerations to take into account when designing (or reviewing) a Patient Information Sheet.
Fees are based on the attendee's organisation as follows:
£0 free for attendees from units within the Institute of Clinical Trials and Methodology (ICTM) which are: • Cancer Research UK & UCL Cancer Trials Centre • Comprehensive Clinical Trials Unit at UCL • Medical Research Council Clinical Trials Unit at UCL • PRIMENT Clinical Trials Unit
The free places require a password to book, if you work within the ICTM please email [email protected] to request this. Emails must be sent from your UCL account and include your name, job title, and the department which you are working in.
Other UCL attendees who are required to pay the course fee can do this by reserving a free place on the online store and then paying by IDT, please email [email protected] who can assist you with this.
£50 for attendees from non-profit organisations
£100 for attendees from for-profit organisations | ||||||||||||||||
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