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STUDY CONSENT FORM Title of Project Evidence-based chiropractic a prospective survey of interventions in a sample of UK chiropractors. Name of Researcher Keith Walker Please initial each box I confirm that I have read and understand the information sheet dated 18/01/2016 version 2 for the above study. I understand that my participation is voluntary and that I am free to withdraw at any time without giving any reason without any consequence to myself. I agree to my anonymised data being used...
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Study consent form is a document that explains the purpose, procedures, risks, and benefits of a research study to potential participants in order to obtain their voluntary agreement to participate.
Researchers conducting a study are required to file a study consent form with their institutional review board (IRB) or ethics committee.
Study consent forms typically include sections for the researchers to provide information about the study, the procedures involved, potential risks and benefits, confidentiality measures, and participant rights. Participants then read and sign the form to indicate their informed consent.
The purpose of study consent form is to ensure that participants are fully informed about the research study, its risks and benefits, and their rights before deciding to participate.
Information that must be reported on a study consent form includes the study's objectives, procedures, risks, benefits, confidentiality measures, contact information for the researchers, and participant rights.
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