Get the free Study Information and Consent Form - Calgary Board of Education

Study Title: A University-Community Partnership to Implement and Evaluate a Whole School Health Promotion Pilot Project in Calgary Schools Principal Investigator: Dr. Penelope Have Population Health

How to fill out study information and consent

Steps to fill out study information and consent:

1. Obtain the necessary forms: Contact the relevant study coordinator or research team to request the study information and consent forms. They can provide you with the required documents.
2. Read and understand the study information: Carefully review the study information provided in the form. It will typically include details about the purpose of the study, the procedures involved, potential risks and benefits, confidentiality, and any compensation or incentives. Take the time to understand the information thoroughly.
3. Seek clarification if needed: If you have any doubts or concerns about the study, reach out to the study coordinator or research team. They are there to address your questions and provide clarification.
4. Provide accurate personal information: Start by entering your personal information accurately. This may include your full name, contact information, date of birth, and any other required details. Make sure to double-check the information for accuracy.
5. Give informed consent: Carefully read the informed consent section of the form. This section explains your rights as a participant in the study, including your ability to withdraw at any time. If you agree to participate, you will need to sign the consent form. By signing, you are confirming that you understand the study and agree to be a part of it voluntarily.
6. Submit the completed forms: After filling out the study information and consent forms, make sure to review them again to ensure all sections are complete and accurate. If any optional sections are included, decide whether you want to provide the requested information.

Who needs study information and consent?

1. Individuals considering participation in a research study
2. Potential participants who want to learn about the study's purpose, procedures, risks, and benefits
3. Researchers conducting the study to fulfill ethical and legal requirements
4. Institutional review boards or ethics committees responsible for ensuring participant safety and informed consent compliance

For pdfFiller’s FAQs

What is study information and consent?

Study information and consent refers to providing detailed information about a research study and obtaining consent from participants before they can participate.

Who is required to file study information and consent?

Researchers or organizations conducting the study are required to file study information and consent.

How to fill out study information and consent?

Study information and consent forms can be filled out by providing accurate details about the study purpose, procedures, risks, benefits, and obtaining participant consent.

What is the purpose of study information and consent?

The purpose of study information and consent is to ensure that participants are fully informed about the study they are participating in, including potential risks and benefits, and to obtain their voluntary consent.

What information must be reported on study information and consent?

Study information and consent forms must include details about the study purpose, procedures, risks, benefits, confidentiality, and contact information for the researchers.

How can I send study information and consent for eSignature?

When you're ready to share your study information and consent, you can swiftly email it to others and receive the eSigned document back. You may send your PDF through email, fax, text message, or USPS mail, or you can notarize it online. All of this may be done without ever leaving your account.

Where do I find study information and consent?

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