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PREADAPTSepsis ICF Version 1.0 20/07/2018PREADAPTSepsis Informed Consent Form v1.0 IRAS ID: 215810 Title of Project: Process Evaluation of the ADAPTSepsis trial (PREADAPTSepsis): Factors influencing
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Who needs preadapt-sepsis informed consent form?

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Anyone who is participating in the preadapt-sepsis program needs to fill out the informed consent form. This includes individuals who have been diagnosed with sepsis or those at risk of developing sepsis. It is essential to understand the program and its potential risks before participating.
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The preadapt-sepsis informed consent form is a document that explains the research study and its potential risks and benefits to participants.
All participants who are taking part in the preadapt-sepsis research study are required to fill out the informed consent form.
Participants can fill out the preadapt-sepsis informed consent form by carefully reading the information provided, asking questions if needed, and signing the document to indicate their understanding and agreement.
The purpose of the preadapt-sepsis informed consent form is to ensure that participants are fully informed about the research study and voluntarily agree to take part.
The informed consent form must include information about the study procedures, potential risks and benefits, confidentiality, participant rights, and contact information for further questions.
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