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Document type: informed consent form (ICF) Document date: 01/29/2021 Title: Mobile Coping Skills Training to Improve Cardiorespiratory Failure Survivors\' Psychological Distress (Blueprint) Identifier:
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Read the informed consent form thoroughly to understand the purpose of the study.
02
Fill in your personal information accurately, including name, contact information, and any other required details.
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Individuals who are participating in a research study or clinical trial need to fill out an informed consent form.
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Informed Consent Form (ICF) is a document provided to potential participants in a research study that describes the information about the study and its risks and benefits.
Researchers conducting a study are required to file an informed consent form (ICF) with their institutional review board (IRB) or ethics committee.
To fill out an informed consent form (ICF), the researcher must carefully explain the study, its procedures, risks, benefits, and obtain the voluntary agreement of the participant to participate.
The purpose of the informed consent form (ICF) is to ensure that participants are fully informed about the study, its risks and benefits, and voluntarily agree to participate.
The informed consent form (ICF) must include information about the study purpose, procedures, risks, benefits, confidentiality, contact information, and voluntariness of participation.
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