Get Informed Consent Instructions And Template - Regis College - Regiscollege

Filling out the Informed Consent Instructions And Template is a crucial part of conducting ethical research. This guide provides a clear and supportive roadmap for completing each section of the form, ensuring that users feel confident and informed throughout the process.

Follow the steps to accurately complete the informed consent form.

1. Click the ‘Get Form’ button to download the informed consent template and open it in your preferred editing tool.
2. Begin by entering the title of your research project in the designated field. Providing a clear and concise title helps participants understand the focus of your study.
3. Fill in the name of the principal investigator (PI) along with their phone number and email. Ensure the contact information is accurate for participants to reach out with any queries.
4. If applicable, list any co-principal investigators (Co-PIs) and student investigators involved in the study. This transparency builds trust with participants.
5. In the introduction section, provide a clear statement about the research study, outlining who is selected for participation, including the eligibility criteria.
6. State the purpose of the study briefly, explaining what the research aims to achieve.
7. In the procedures section, detail what participants will be asked to do and the expected duration of their involvement. Include specifics about the frequency and length of any sessions.
8. Outline the potential benefits of the research, highlighting how the findings may positively impact participants or society.
9. Discuss any potential risks associated with participation, ensuring clarity about how risks will be minimized.
10. If compensation is offered, explain the payment structure, including the amount and timing of disbursements.
11. Indicate that participation in the study entails no cost to the participants.
12. Insert a statement regarding the right to refuse or withdraw participation and clarify that such actions will not affect academic or employment standing.
13. Explain the measures taken to ensure privacy and confidentiality of participant information throughout the research process.
14. Provide additional contact information for the researcher and the chairperson of the Regis College Institutional Review Board for participants to voice any concerns.
15. In the contact information section, fill in the necessary details for the PI and the IRB chairperson.
16. Ensure all signatory sections are completed, collecting necessary signatures from participants and the researcher.
17. Finally, save your changes, download, print, or share the completed form as required to finalize the consent process.

Complete your informed consent documents online to ensure ethical and organized research.