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You should state how long the participant will be involved in the research, how long the research will last (if this is different), how often they will need to participate and for how long each time. You should detail whether travel expenses will be reimbursed.
The consent form is the document on which participants give their written consent to take part in the research. Consent may also be provided verbally or implied, in which case a written consent form will not be needed, but a participant information sheet will be required.
You should state how long the participant will be involved in the research, how long the research will last (if this is different), how often they will need to participate and for how long each time. You should detail whether travel expenses will be reimbursed.
Any signed consent forms will need to be retained for 3 years after the conclusion of your study. Forms that are not signed are considered information sheets and do not need to be archived, although one copy should be saved for your records for 3 years.
Use patient friendly text personal pronouns such as we and you. If it is difficult to avoid using medical terminology such as nuclear medicine, explain what each term means. Information should be complementary to other information ie letters and leaflets and be relevant to individuals.
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The participant information sheet is used to explain the purpose of the research and what participants will be required to do /how participants will be involved. It should be in plain English, using language appropriate to the target audience.

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