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I consent to participate in the research project and the following has been explained to me: the research may not be of direct benefit to me. my participation is completely voluntary. my right to withdraw from the study at any time without any implications to me.
For an ethically valid consent, information provided to a research subject should include, but not be limited to: information about the health condition for which the research is proposed; details of the nature and purpose of the research; the expected duration of the subject's participation; a detailed description of ...
The consent form must include: A statement that the study involves research. ... Purpose of the research. ... Procedures. ... Risks or discomforts to the subject. ... Benefits of the research to the subject. ... Treatment Alternatives. ... Costs of Participation. ... Confidentiality.
A consent form was presented and signed by the parent. Patients were requested to complete the questionnaire immediately and sign and return the consent form by mail.
Make certain that the formal letter/email has a clear consent heading. Describe the respondents' specifications/requirements (if any). Indicate the length of the program or participation. Ensure that the letter includes relevant names and other facts such as addresses and contact information for the respective parties.