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STUDY INFORMATION AND CONSENT FORM (EXPERIMENT GROUP) INVITATION TO PARTICIPANTS TO PARTICIPATE IN THE RESEARCH STUDY DATE: Dear Sir/Madam, My name is AHMED Usman Abbey, a physiotherapist and a PhD
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Step 1: Start by gathering all necessary study information, such as the purpose of the study, any specific instructions or requirements, and any additional materials or documents that may be needed.
02
Step 2: Begin filling out the study information form by providing accurate and complete details. This may include personal information, contact information, demographic information, medical history, and any other relevant details.
03
Step 3: Review the consent form carefully. Make sure you understand the rights and responsibilities associated with participating in the study. If you have any questions or concerns, seek clarification from the study coordinator or researcher.
04
Step 4: Sign the consent form if you agree to participate in the study. Ensure that your signature is clear and legible. If you are under 18 or legally unable to provide consent, make sure a parent or guardian signs on your behalf.
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Step 5: Submit the completed study information form and consent form to the appropriate person or entity, as instructed. Make sure to retain a copy for your records.

Who needs study information and consent?

01
Anyone who wants to participate in a study or research project needs to provide study information and consent. This includes individuals of all ages and backgrounds, as long as they meet the specified eligibility criteria. In some cases, parental or guardian consent may be required for minors or individuals who are unable to provide consent themselves.
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Study information and consent is a document that outlines the details of a research study, including its purpose, procedures, risks, and benefits, and obtains participant's consent to participate.
Researchers conducting a study are required to submit study information and consent to the relevant ethics committee.
Study information and consent forms can be filled out by providing accurate and complete information about the study, its procedures, risks, benefits, and obtaining participant's signatures.
The purpose of study information and consent is to ensure that participants are fully informed about the research study, its procedures, risks, and benefits, and voluntarily consent to participate.
Study information and consent must include details of the study, its purpose, procedures, risks, benefits, confidentiality, participant's rights, and contact information for researchers.
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