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Participant Information Sheet Title: Opioid Prescriptions and usage After Surgery (OPERAS): Protocol for a prospective multigenre observational cohort study of the prescription and usage of opioids

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How to fill out participant information and consent

01

To fill out participant information and consent, follow these steps:

02

Start by gathering all the necessary information about the participant, such as their full name, contact details, date of birth, and any other relevant personal information required.

03

Prepare a consent form that outlines the purpose of collecting the participant information, how it will be used, and any potential risks or benefits associated with it.

04

Clearly explain the consent form to the participant, ensuring they understand all the terms and conditions.

05

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

06

Ask the participant to sign and date the consent form, indicating their willingness to share their information.

07

If the participant is a minor or lacks the legal capacity to provide consent, make sure to obtain informed consent from their legal guardian or parent.

08

Safely store the participant information and consent forms in a secure location, ensuring confidentiality and compliance with data protection laws.

09

Regularly review and update the participant information and consent as necessary, maintaining accurate records throughout the process.

Who needs participant information and consent?

01

Any organization or individual conducting research, surveys, clinical trials, or any activity that involves collecting personal information from participants requires participant information and consent.

02

Examples of entities that may need participant information and consent include academic institutions, medical facilities, market research companies, and government agencies.

03

It is essential to obtain participant information and consent to protect the rights and privacy of individuals, ensure ethical practices, and comply with legal and regulatory requirements.

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What is participant information and consent?

Participant information and consent refers to the details and permission obtained from individuals who are participating in a study, experiment, or research project.

Who is required to file participant information and consent?

Researchers, scientists, or any organization conducting a study that involves human participants are required to file participant information and consent.

How to fill out participant information and consent?

Participant information and consent forms are typically filled out by providing details about the study, potential risks, benefits, and obtaining the participant's signature indicating their consent to participate.

What is the purpose of participant information and consent?

The purpose of participant information and consent is to ensure that individuals are fully informed about the study they are participating in, including any potential risks, and to obtain their voluntary agreement to take part.

What information must be reported on participant information and consent?

Participant information and consent forms typically include details about the study objectives, procedures, risks, benefits, confidentiality, and how data will be used.

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