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PATIENT INFORMATION SHEET AND INFORMED CONSENT FORM (for adult subjects and interventional studies) 1. Title of study: Effectiveness of Group Cognitive Behavioral Therapy on Pain, Functional Disability
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How to fill out consent form for non-interventional

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Step 1: Start by reading the consent form thoroughly to understand its purpose and the information it requires.
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Step 2: Provide your personal details, such as your name, contact information, and date of birth, in the designated sections of the form.
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Step 3: Review the study or research details mentioned on the consent form. Make sure you understand the objectives, procedures, potential risks, benefits, and confidentiality aspects.
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Step 4: If you have any questions or concerns, reach out to the researcher or study team before proceeding further.
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Step 5: If you are satisfied and agree to participate, sign and date the consent form at the appropriate place.
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Step 6: In case you are unable to sign the form yourself due to any reason, you may provide a thumbprint or an alternative method of indicating your consent.
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Step 7: Keep a copy of the signed consent form for your records.
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Step 8: If you change your mind later and no longer wish to participate, notify the researcher or study team immediately.
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Step 9: Remember that your participation is completely voluntary, and you have the right to withdraw at any point without any penalty or obligation.

Who needs consent form for non-interventional?

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Anyone who wishes to participate in a non-interventional study or research project will need to fill out a consent form. This includes individuals who meet the study's eligibility criteria and voluntarily choose to participate. Consent forms ensure that participants are fully informed about the study and its implications before agreeing to take part.
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A consent form for non-interventional studies is a document that outlines the nature of the study, the procedures involved, and the rights of participants, ensuring that they are fully informed before agreeing to participate.
Researchers or sponsors conducting non-interventional studies involving human participants are required to file a consent form.
To fill out a consent form, provide clear and concise information about the study, including its purpose, procedures, risks, and benefits, and ensure participants can ask questions before signing.
The purpose of the consent form for non-interventional studies is to protect the rights of participants by ensuring they are adequately informed about the study and consent voluntarily.
The information that must be reported includes the study's purpose, procedures, potential risks and benefits, confidentiality assurances, and the right to withdraw at any time.
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