Informed Consent Form/information Letter

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TEMPLATE – INFORMED CONSENT FORM/INFORMATION LETTER
Include or exclude information as applicable.
Item #s are highlighted to reference the CREO guidelines. You should not include these
highlighted item numbers in your form/letter.
“INFORMED CONSENT FORM/INFORMATION LETTER”
1. Title of project
3. “You are invited to participate in a research study”. 3a. “The purpose of this study is …”
2. “This research project is being conducted by …” (describe the researcher(s) and their
affiliation).
INFORMATION
3d. Describe all procedures, preferably in chronological order, which will be employed in
the project.
3e. State the amount of time required of the participant per session and for the total
duration of the study.
If applicable to your study, describe:
3b. Description of the participants
3c. Selection of participants
12. The number of participants that will be participating in the research.
13. Information concerning taping or filming.
14. A disclaimer for the use of deception.
3f, 3g, 3h, & 15. RISKS
List the foreseeable risks or discomforts, if any, of each of the procedures to be used in the
study, and any measures which will be used to minimize the risks.
3i. BENEFITS
List the benefits you anticipate will be achieved from this research, either to the
participants, others, communities or the body of knowledge.
4. CONFIDENTIALITY
Describe how the confidentiality and anonymity of participants will be ensured. Describe
who has access to the data, where the data will be kept, and what will happen to the data
when the project is finished. Describe the extent, if any, to which confidentiality of records
identifying the participant will be maintained. OR, explain when and how confidentiality
will be broken. Provide a statement about the ways in which the research results will be
published or distributed. Participants must be told if quotations will be used in any write-
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