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Participant Enrollment Informed Consent Form for Intervention Participants. Study title: Understanding the role of food insecurity and depression in nonadherence to Option B+ among perinatal Kenyan
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How to fill out participant enrolment informed consent

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How to fill out participant enrolment informed consent

01
Begin by reading the participant enrolment informed consent form carefully.
02
Fill in the personal details of the participant, such as their name, address, contact information, and date of birth.
03
Understand and acknowledge the purpose of the study or research being conducted.
04
Review and comprehend the potential risks and benefits associated with participation.
05
Sign and date the consent form in the provided spaces.
06
If the participant is unable to provide consent themselves, ensure that a legally authorized representative fills out the form on their behalf.
07
Keep a copy of the consent form for your records.
08
Make sure to ask any questions or clarifications before signing the form.

Who needs participant enrolment informed consent?

01
Anyone who wishes to participate in a study or research project that requires informed consent from the participants.
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Participant enrolment informed consent is the process by which participants in a study are fully informed of the purpose, risks, benefits, and procedures involved in the study before deciding to participate.
Researchers conducting the study are required to file participant enrolment informed consent.
Participant enrolment informed consent should be filled out by providing all necessary information to the participants and obtaining their signature to indicate their understanding and agreement.
The purpose of participant enrolment informed consent is to ensure that participants have full knowledge of the study before agreeing to participate, and to protect their rights and well-being.
Participant enrolment informed consent must include information on the study's purpose, risks, benefits, procedures, confidentiality, and the right to withdraw.
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