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  2. Learn how to write a clear and simple information sheet and consent form for research participants, with examples and guidance from UCL Research Ethics. Find out what to include, how to present it, and what to avoid in your recruitment documents.

  3. The information provided to participants is crucial for a number of reasons: It explains to individuals everything that will happen to them, should they consent to participate; it allows them to weigh up the risks and benefits of taking part; and it ensures that the information provided to them is fully documented from a legal perspective.

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  4. Aug 21, 2023 · Participant Information Design and Review Principles. Last updated on 21 Aug 2023. The Design and Review Principles have been created to show researchers and Research Ethics Committees (REC) what the important ethical considerations are for participant information.

  5. Participant Information Sheets. The Participant Information Sheet (PIS) should be a clear and simple document, on headed paper with the University Crest (or equivalent for other institutions), that would be easily understood by those to whom it is aimed; for example, it should be age-appropriate.

  6. Informing participants and seeking consent. Last updated on 25 Mar 2024. With the Medical Research Council (MRC) we provide an online tool that gives guidance on consent and the preparation of information for participants.

  7. The guidance covers consent in adults, children, young people and adults not able to consent for themselves (in both emergency and non-emergency situations) and takes into account UK-wide requirements.

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