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Confidential upon completionTrial Number:Insert Trust logoADEPP TRIAL CONSENT FORM Antidepressant for the prevention of Depression following first episode Psychosis trialPlease initial each box to indicate
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Informed consent is required for any individual who is participating in a research study, clinical trial, medical procedure, or any other situation where their participation involves potential risks or benefits.
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Informed consent is a process for getting permission before conducting a healthcare intervention on a person. It requires the healthcare provider to explain the risks, benefits, and alternatives to the patient.
Healthcare providers are required to obtain informed consent from patients before performing any medical procedures.
Informed consent forms are typically filled out by the patient or their legal guardian, after the healthcare provider has explained the procedure and risks involved.
The purpose of informed consent is to ensure that patients are fully informed about the medical procedures they are undergoing, and to respect their autonomy in making decisions about their own health care.
Informed consent forms typically include information about the procedure being performed, potential risks and benefits, alternatives, and confirmation that the patient understands and consents to the treatment.
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