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Get (irb) Sample Informed Consent Letter - Uvu - Uvu
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How to use or fill out the (IRB) Sample Informed Consent Letter - UVU - Uvu online
This guide provides a step-by-step approach to completing the (IRB) Sample Informed Consent Letter for research studies at Utah Valley University (UVU). It is designed to assist users in understanding each component of the form to ensure a clear and comprehensive consent process.
Follow the steps to effectively complete the informed consent letter.
- Click the ‘Get Form’ button to obtain the form and open it in the document editor.
- Begin by inputting the title of the study at the designated section. This title should accurately represent the research proposal.
- Fill in the principal investigator's details, including their name, department, address, phone number, and email. Ensure that all contact information is current and accurate.
- In the background section, explain the invitation for participation and its purpose clearly. This should help potential participants understand the research significance.
- Outline the study procedures, including the expected time commitment from the participants. Be specific about what their involvement entails.
- Detail any risks associated with the study. Clearly represent that risks are minimal and describe what participants might experience.
- Enumerate the potential benefits of participating in the study, even if they may not directly benefit the participants.
- Mention alternative procedures, explaining what participants can do if they choose not to take part.
- Include a confidentiality statement that outlines how participants' data will be protected, including anonymous options if applicable.
- Provide contact information for the researcher and mention the purpose of the Institutional Review Board (IRB). Include a contact number for participant rights inquiries.
- Clarify that participation is voluntary, detailing the rights of participants to withdraw from the study at any time without repercussions.
- Address unforeseen risks, stating that potential unanticipated risks could occur but that measures will be taken to minimize them.
- Confirm that there are no costs or monetary compensations related to participation.
- Conclude the letter with a consent section requiring the participant's signature and date, confirming their understanding of the study.
- After completing the form, users can save their changes, download the document, print it, or share it as needed.
Start completing the informed consent letter online today to ensure a clear communication process for your research study.
It is the PI's responsibility to oversee and ensure proper completion of information to the IRB including the original submission and all revisions requested during IRB review.
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