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This Informed Consent Form outlines the details regarding participation in a research study aimed at testing a new self-management treatment for low back pain in individuals aged 50 and over. It includes information about the study\'s purpose, procedures, possible benefits and risks, and the handling of protected health information.

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What is informed consent form?

An informed consent form is a document that outlines the details of a medical procedure or research study, ensuring that participants understand the risks, benefits, and their rights before agreeing to participate.

Who is required to file informed consent form?

Researchers and healthcare providers who conduct clinical trials or medical procedures 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, the participant must read the document carefully, ask questions if needed, and then sign it to indicate their understanding and agreement to participate.

What is the purpose of informed consent form?

The purpose of an informed consent form is to ensure that individuals make informed decisions about their participation in research or medical treatments, while protecting their autonomy and rights.

What information must be reported on informed consent form?

The informed consent form must include information about the study or procedure, its purpose, potential risks and benefits, the right to withdraw, confidentiality, and contact information for questions.

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