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Insert Trust/APT Service Logo INFORMED CONSENT FORM Full Study Title: Clinical and cost-effectiveness of Alphabetic AID Cranial Electrotherapy Simulations (CES); a naturalistic study in patients with

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How to fill out page 1 informed consent

01

Step 1: Start by reading the instructions carefully.

02

Step 2: Provide your personal details such as name, address, and contact information.

03

Step 3: Clearly state the purpose of the informed consent form.

04

Step 4: List any risks or potential side effects associated with the study or procedure.

05

Step 5: Include a section for the participant to sign and date the form.

06

Step 6: Make sure to provide contact information for any questions or concerns.

07

Step 7: Review the completed form to ensure all necessary information is included.

Who needs page 1 informed consent?

01

Anyone who is participating in a study or medical procedure that requires informed consent should fill out page 1 of the informed consent form.

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What is page 1 informed consent?

Page 1 informed consent is a document that outlines the terms and conditions of a research study or medical procedure, typically signed by the participant or patient.

Who is required to file page 1 informed consent?

Researchers, medical professionals, or institutions conducting the study or procedure are required to file page 1 informed consent.

How to fill out page 1 informed consent?

Page 1 informed consent should be filled out by providing accurate and detailed information about the study or procedure, risks and benefits, and obtaining the signature of the participant or patient.

What is the purpose of page 1 informed consent?

The purpose of page 1 informed consent is to ensure that participants or patients are fully informed about the study or procedure, understand the risks and benefits, and voluntarily agree to participate.

What information must be reported on page 1 informed consent?

Page 1 informed consent must include details about the study or procedure, risks and benefits, confidentiality, participant rights, and contact information for questions or concerns.

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