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This Informed Consent Form provides information about a research study that aims to learn more about physical activity behavior intervention as part of physical rehabilitation after total knee arthroplasty (TKA). Participants will undergo various tests and interventions over a study period of approximately 39 months and are informed of the procedures, potential risks, benefits, and confidentiality measures related to their participation.
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How to fill out informed consent form

01
Read the informed consent form carefully to understand its purpose.
02
Provide personal information as required, such as your name and contact details.
03
Review the details of the study or procedure being proposed, including its risks and benefits.
04
Ensure that all questions related to the study or procedure are answered to your satisfaction.
05
Indicate your willingness to participate by signing and dating the form.
06
Keep a copy of the signed consent form for your records.

Who needs informed consent form?

01
Participants in clinical trials or medical research.
02
Patients undergoing medical procedures or treatments.
03
Individuals involved in psychological studies or surveys.
04
Parents or guardians consenting on behalf of minors.
05
Any person participating in educational or behavioral research.
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An informed consent form is a document that provides potential participants in a study with detailed information about the research, including its purpose, procedures, risks, benefits, and the right to withdraw, enabling them to make an informed decision about their participation.
Researchers conducting studies involving human subjects are required to file informed consent forms to ensure that participants are fully informed and agree to take part in the research.
To fill out an informed consent form, provide clear and concise information about the study, including the purpose, procedures, risks, benefits, confidentiality, and contact information. Ensure that participants are given adequate time to read the form and ask questions before signing.
The purpose of an informed consent form is to protect the rights and welfare of research participants by ensuring they understand what they are engaging in and the implications of their participation in the study.
An informed consent form must report information including the study's purpose, procedures, potential risks and benefits, confidentiality measures, voluntary participation, and contact information for questions or concerns.
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