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This document provides information regarding the School-based eHealth NCD Prevention Program aimed at enhancing adolescents\' knowledge, attitudes, and practices about non-communicable disease (NCD) prevention, specifically focusing on diet and physical activity. It outlines the consent process for participating in focus group discussions and interviews with students, parents, and teachers, detailing the study\'s purpose, procedures, potential risks, benefits, and confidentiality assurances.

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How to fill out informed consent form

01

Start with the title of the study or procedure.

02

Provide a brief introduction about the purpose of the study or procedure.

03

Outline the risks and benefits associated with participation.

04

Describe the participation requirements and what is expected from the participant.

05

Include information on confidentiality and how the data will be used.

06

Provide contact information for questions or concerns.

07

Include a section for the participant's signature along with the date.

Who needs informed consent form?

01

Participants in clinical trials.

02

Patients undergoing medical procedures.

03

Individuals taking part in psychological research.

04

Subjects in educational studies.

05

Participants in surveys involving personal data.

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What is informed consent form?

An informed consent form is a document that provides potential participants in a study or procedure with information about the research or treatment, ensuring they understand and agree to the participation based on the details provided.

Who is required to file informed consent form?

Researchers, medical professionals, or organizations conducting studies or medical procedures involving human participants are required to file informed consent forms.

How to fill out informed consent form?

To fill out an informed consent form, one must read the document carefully, provide any requested personal information, ensure understanding of the study's purpose, risks, benefits, and sign the form to indicate consent.

What is the purpose of informed consent form?

The purpose of an informed consent form is to protect the rights of participants, ensuring they are fully informed about the nature, risks, and benefits of a study or procedure before agreeing to participate.

What information must be reported on informed consent form?

The informed consent form must report information including the study's purpose, procedures, risks, benefits, confidentiality, voluntary nature of participation, and contact information for questions.

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