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INFORMED CONSENT AND HELPFUL INFO Informed consent is important! It means that you have fully understood the psychological services being offered, including its risks and limitations, and have voluntarily
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Ensure the participant understands the purpose of the study
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Informed consent is needed by participants in research studies, medical treatments, clinical trials, and any situation where a person is required to make an informed decision about their participation or treatment.
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Informed consent is a process for ensuring that a patient or research participant understands the risks and benefits of a treatment or study before making a decision.
Healthcare providers, researchers, and institutions conducting studies or providing treatments are required to obtain informed consent.
Informed consent forms are typically filled out by the healthcare provider or researcher, reviewed with the patient or participant, and signed by both parties.
The purpose of informed consent is to respect the autonomy and decision-making of patients or participants, and to ensure they understand the risks and benefits involved.
Informed consent forms must include details about the study or treatment, potential risks and benefits, alternative options, and the patient's right to withdraw consent.
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