Participant Information Sheet and Consent Form Templates.
Guidance on Completing a Participant Information Sheet Central to human subject research is the informed consent process. This process must ensure that research participants are provided with all the relevant information they need in order to decide if they would like to participate in a study. It is therefore important that information given to participants, before obtaining their written.
The UEC has drafted templates for researchers to use as a starting point when developing a Participant Information Sheet and Consent Form for their projects. It is important that you tailor the Participant Information Sheet and Consent Form for your participant group and project. For example, use appropriate language for the age and understanding of your participant group, remove paragraphs.
While it is sometimes possible to obtain oral consent for research (e.g. where data is collected through audio or video recordings) it is normally most appropriate to obtain consent through provision of a participant information sheet (PIS) and consent form in either written or electronic form.
Participant Information Sheet ABI group age 11-15. Version 6 24.07.14 One of your parents or someone who looks after you will also be asked to fill in a short questionnaire about you, which they can post back to the researcher.
Participant Information Sheet (Title of Project) Please take some time to read this information. and ask. questions if anything is unclear. Contact details can be found at the end of this document.
Write a front page for the Participant Information Sheet like an example below. Involve a family member to help ensure these issues are explained (and understood). Involve the patient’s clinician or patient to help ensure these issues are explained (and understood).
Participants Information Sheet. Study Title: Patient Decision Aid for Type 2 Diabetes. Protocol Ref: ZH25. Version: V2-030809. Part 1. We would like to invite you to take part in an evaluation of the Patient Decision Aid for Type 2 Diabetes (PANDAs) study. The evaluation process involves audiotaping your consultation with the Health Care Professional. It will also include a 30 minute.