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INFORMED CONSENT FORM The effect of a topical pain relieving gel vs. a placebo on chronic low back pain walking gait characteristics and pain You have been invited to take part in this study. It is
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The informed consent form is a document that provides potential participants with relevant information about a research study or medical procedure so that they can make an informed decision.
Researchers, healthcare providers, or individuals conducting a study or procedure that involves human subjects are required to file an informed consent form.
To fill out an informed consent form, one must provide detailed information about the study or procedure, risks and benefits involved, confidentiality measures, participant rights, and obtain the signature of the participant.
The purpose of an informed consent form is to ensure that participants are aware of the risks and benefits involved in a study or procedure, understand their rights, and voluntarily agree to participate.
The informed consent form must include information about the study objectives, procedures involved, potential risks and benefits, confidentiality measures, participant rights, and contact information for any questions or concerns.
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