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INFORMED CONSENT Forested Number: FIS202002 Protocol version: 1.0 Date: 08.07.2020 Research title: Using the App as a guide to lumbopelvic stability exercises in patients with chronic stroke: a pilot
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Read the form carefully to understand the purpose and implications of providing consent.
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The informed consent form PGina is a document that provides information about a research study, allowing participants to understand the purpose, procedures, risks, and benefits, ensuring they can make an informed decision regarding their participation.
Researchers conducting studies that involve human participants are required to file an informed consent form PGina to ensure ethical compliance and participant protection.
To fill out the informed consent form PGina, researchers should provide clear and comprehensive information about the study, including the research purpose, procedures, risks, benefits, confidentiality assurance, and the participant’s right to withdraw consent at any time.
The purpose of the informed consent form PGina is to ensure that participants are fully aware of what the study entails and to obtain their voluntary agreement to participate in the research.
The informed consent form PGina must report information such as study objectives, procedures, potential risks and benefits, data confidentiality measures, and contact information for questions or concerns.
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