Get Uhn Reb Consent Form Guidance Document ... - Uhnresearch.ca - Uhnresearch

This guide provides clear, step-by-step instructions on how to successfully complete the UHN REB Consent Form Guidance Document. Whether you are new to this process or have experience, this guide aims to streamline your form-filling experience with helpful tips and insights.

Follow the steps to fill out the UHN REB Consent Form effectively.

1. Press the ‘Get Form’ button to obtain the form and open it for editing.
2. In the first section, enter the document title, ensuring to specify any subgroups within your study for clarity.
3. Next, input the full study title as it appears in your protocol, and include the protocol number if applicable. Adding a simplified lay term title is advisable if the official title is complex.
4. Provide the name, title, and telephone number of the Principal Investigator. Only use 'Dr.' for licensed medical doctors and 'Nurse' for licensed nurses in Canada. Other investigators should be referenced by their credentials and country of practice.
5. If applicable, list the Co-Investigators. Remember that revisions must be made if there are changes in co-investigators.
6. Include the 24-hour contact information for clinical trials. This may be a pager number and must provide clear instructions for contacting the relevant on-call physician, if necessary.
7. Document the full name of all sponsors and funding sources, ensuring not to list UHN as a sponsor.
8. Complete the introduction section using language compliant with the UHN Consent Form Template.
9. In the background/purpose section, detail the study's background, purpose, reasons for participation, usual treatment, investigational interventions, number of participants, and study duration.
10. Whenever relevant, describe the study design, including any necessary definitions and methodologies utilized during the study.
11. List study procedures clearly including visit types, participant requirements, and any biological sample quantities.
12. Reiterate participants’ voluntary participation rights and withdrawal procedures to ensure they are fully informed.
13. Identify any potential risks involved with the study and opt for lay language to describe them clearly.
14. Outline any possible benefits to the participant or contributions to medical knowledge resulting from the study.
15. Conclude by highlighting participants’ rights, ensuring transparency regarding costs, confidentiality and any conflicts of interest.
16. Before submission, ensure all sections are correctly filled, and remember to proofread the document for clarity and correctness.
17. Once completed, users can save their changes, download, print, or share the form as necessary.

Complete your UHN REB Consent Form online today to ensure your participation in vital research.