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Supporting file _Section 1. Appendixes Three: Information sheet, Consent and Questionnaire for Research (Indepthinterview for the service provider)Information Sheet and Consent to Participate in ResearchGate: How
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Start by reading the informed consent form thoroughly to understand its contents and purpose.
02
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Who needs example this informed consent?

01
Anyone participating in a study or procedure that requires informed consent.

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An informed consent document is a form that outlines the details of a study or treatment, ensuring that participants understand the risks, benefits, and procedures involved before agreeing to participate.
Researchers or institutions conducting studies involving human subjects are required to file informed consent forms to ensure ethical standards are met.
To fill out an informed consent form, participants should read the document carefully, provide any required personal information, and sign to acknowledge their understanding and agreement.
The purpose of informed consent is to protect participants' rights and ensure they have a full understanding of what they are agreeing to, promoting ethical research practices.
The information reported should include the study's purpose, procedures, risks, benefits, confidentiality measures, and the right to withdraw at any time.
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