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REC Reference Number: 20/SC/0208 Patient Identification Number for this trial: ___ Patient Initials:INFORMED CONSENT Forested Title: Prospective longitudinal assessment in a COVID-19 infected cohort
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How to fill out informed consent and trial

01
Provide detailed information about the study including purpose, procedures, risks, and benefits.
02
Explain the voluntary nature of participation and the right to withdraw at any time.
03
Ensure that the participant understands the information provided and can make an informed decision.
04
Have the participant sign the consent form to indicate their agreement to participate.

Who needs informed consent and trial?

01
Informed consent and trial are required for all participants involved in research studies, clinical trials, medical procedures, and experiments.

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Informed consent and trial is a process where participants are given all the necessary information about a clinical trial before deciding to participate.
Researchers conducting the clinical trial are required to file the informed consent and trial.
Informed consent and trial forms are typically filled out by the research team and signed by the participant.
The purpose of informed consent and trial is to ensure that participants are fully informed about the risks and benefits of participating in a clinical trial.
The informed consent and trial form must include details about the study objectives, procedures, risks, benefits, and participant rights.
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