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INFORMED CONSENT FORM STUDY: Sweat, Grit, and Emotions: Understanding the TugofWar Between Mental Health Benefits and Drawbacks in UltraEndurance Sports There are two sections in this form. Section

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How to fill out informed consent form

01

Read the informed consent form carefully to understand its purpose.

02

Fill in personal information such as name, date of birth, and contact information where required.

03

Review the details of the study or treatment you are consenting to, including risks and benefits.

04

Indicate your understanding by signing and dating the form in the designated areas.

05

Ask any questions you may have regarding the form or the study before submitting.

06

Keep a copy of the signed informed consent form for your records.

Who needs informed consent form?

01

Individuals participating in clinical trials or research studies.

02

Patients undergoing medical procedures or treatments.

03

Participants in surveys or behavioral research.

04

Any situation where personal data is collected for research or evaluation purposes.

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What is informed consent form?

An informed consent form is a document that outlines the details of a study or treatment, ensures that participants understand the risks and benefits, and confirms their agreement to participate.

Who is required to file informed consent form?

Researchers or organizations conducting studies involving human participants are required to file an informed consent form.

How to fill out informed consent form?

To fill out an informed consent form, provide clear information about the study or treatment, include details about risks, benefits, and participant rights, and ensure that participants sign the document voluntarily.

What is the purpose of informed consent form?

The purpose of an informed consent form is to protect participants by ensuring they are aware of what they are consenting to and to provide legal documentation of their agreement.

What information must be reported on informed consent form?

An informed consent form must report information such as the purpose of the study, procedures involved, potential risks and benefits, confidentiality assurances, and participants' rights.

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