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PARTICIPANT INFORMATION SHEET & CONSENT FORM (PICK) PROJECT TITLE: Effect of Nutritional Interventions on Autopay (The NINA study) HUMAN RESEARCH ETHICS COMMITTEE APPROVAL NUMBER: H2021154 PRINCIPAL

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How to fill out participant information sheet consent

01

Provide the participant with the information sheet consent form.

02

Explain to the participant the purpose of the study and what their involvement entails.

03

Have the participant read through the information sheet carefully.

04

Answer any questions or concerns the participant may have about the study.

05

Ask the participant to sign and date the consent form if they agree to participate.

06

Provide a copy of the signed consent form to the participant for their records.

Who needs participant information sheet consent?

01

Any individual who is invited to participate in a research study or clinical trial will need to fill out a participant information sheet consent.

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What is participant information sheet consent?

Participant information sheet consent is a document that explains the purpose and details of a research study to potential participants, allowing them to make an informed decision about participating.

Who is required to file participant information sheet consent?

Researchers conducting a study involving human subjects are required to provide and file participant information sheet consent.

How to fill out participant information sheet consent?

Participant information sheet consent should be filled out by including all relevant study details such as purpose, risks, benefits, procedures, confidentiality, and contact information for questions or concerns.

What is the purpose of participant information sheet consent?

The purpose of participant information sheet consent is to ensure that potential participants understand the research study, their rights as participants, and can make an informed decision about whether or not to participate.

What information must be reported on participant information sheet consent?

Participant information sheet consent must include details about the study's purpose, procedures, risks, benefits, confidentiality measures, contact information, rights of participants, and how to withdraw.

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