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This form is used to obtain consent from relatives for a patient to participate in the STICH II clinical study on brain haemorrhage treatment. It includes a confirmation of understanding and discussion

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How to fill out stich ii relative assent

How to fill out STICH II Relative Assent Form

01

Read the instructions carefully.

02

Provide the date at the top of the form.

03

Fill in the participant's initials and last name.

04

Include the relationship of the individual filling out the form to the participant.

05

Indicate your understanding of the study's purpose.

06

Sign and date the form at the designated areas.

Who needs STICH II Relative Assent Form?

01

Family members or guardians of participants in the STICH II study.

02

Individuals who are providing consent on behalf of a participant unable to provide assent.

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What is STICH II Relative Assent Form?

The STICH II Relative Assent Form is a document used in research studies to obtain consent from relatives of participants regarding the involvement of their loved ones in a study.

Who is required to file STICH II Relative Assent Form?

The STICH II Relative Assent Form is required to be filed by researchers or institutions conducting studies that involve individuals unable to provide informed consent due to medical conditions, where a relative gives assent on their behalf.

How to fill out STICH II Relative Assent Form?

To fill out the STICH II Relative Assent Form, one must provide the necessary personal information about the participant and the relative, explain the study details, confirm understanding and agreement, and ensure that the form is signed and dated by the relative.

What is the purpose of STICH II Relative Assent Form?

The purpose of the STICH II Relative Assent Form is to ensure ethical compliance in research by obtaining agreement from family members for the participation of individuals who are unable to consent for themselves.

What information must be reported on STICH II Relative Assent Form?

The STICH II Relative Assent Form must report information including the participant's details, the relative's information, a description of the study, potential risks and benefits, and a declaration of the relative's understanding and consent.

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