LETTER OF INFORMATION FOR CONSENT TO PARTICIPATE IN RESEARCH Title of Study.

Sample letter of informed consent for research participants. Name of the Principal Investigator from the European University Institute EUI in Florence Italy. They are long only because they contain guidance and explanations which are for you and which you will not include in the informed consent forms that you develop and provide to participants in your research. Principle Investigator Affiliation and Contact Information.

Please refer to the document entitled components of informed consent. That is we are interested in studying how motor. The participant letter of invitation participant information sheet signed informed consent declaration and complete questionnaire will be collected and taken to be analysed.

Sample informed consent form for research participant. INFORMED CONSENT FORM Thank you for agreeing to participate in this study which will take place from October 8 2004 to December 8 2004. Do not be concerned by the length of these templates.

Sample Letter Of Informed Consent For Research Participants. Letter of Introduction and Informed Consent Form. All research participants must give their permission to be part of a study and they must be given pertinent information to make an informed consent to participate.

If you have any questions regarding your rights as a participant in this research andor concerns about the study or if you feel under any pressure to enroll or to continue to participate in this study you may contact the University of Missouri Campus Institutional Review Board which is a group of people who review the research studies to protect participants rights at 573 882-9585 or. This statement describes the purpose and procedures of the study. The purpose of this study is.

You are also welcome to contact myself at any stage during the research project with any questions you may have. If your consent letter is more than one page the footer should also include a space for the participants initials eg the footer in this document. This means you have provided your research participants with everything they need to know about the study to make an informed decision about participating in your research.