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Community and Provider driven Social Accountability Intervention (CaPSAI) Project Informed consent and assent forms: GHANA Contents Prospective Cohort Followup of New Contraceptive Users..............................................................
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How to fill out informed consent and assent

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How to fill out informed consent and assent

01
Provide a brief explanation of the research study, including its purpose and procedures.
02
Clearly outline the risks and benefits involved in participating in the study.
03
Explain the participant's rights, including the right to withdraw from the study at any time.
04
Ensure that the participant understands the information provided and has the opportunity to ask any questions.
05
Have the participant sign the consent form (or assent form for minors) to indicate their willingness to participate.

Who needs informed consent and assent?

01
Informed consent is required for all participants in a research study, regardless of age or background.
02
Assent is needed for minors, usually those under the age of 18, in addition to parental or guardian consent.
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Informed consent is a process by which a participant voluntarily confirms their willingness to participate in a research study, after being informed of all relevant aspects that may affect their decision. Assent is similar but refers specifically to the agreement of minors or individuals who are not fully able to provide informed consent themselves, indicating that they understand the research and agree to participate.
Researchers and institutions conducting studies involving human subjects are required to file informed consent and assent to ensure ethical standards and the protection of participants.
To fill out informed consent and assent, researchers should provide a clear, comprehensive document outlining the study's purpose, procedures, risks, benefits, and the rights of participants. Participants or their guardians should then read, understand, and sign the documents to indicate their agreement.
The purpose of informed consent and assent is to ensure that participants are fully aware of the nature of the study, understand their rights, and willingly participate in the research without coercion.
Informed consent and assent must report information such as the study's purpose, procedures, potential risks and benefits, confidentiality measures, the right to withdraw, and contact information for questions.
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