IRB Minimal Risk Study Application

1. Study Title and Investigator Information

Study Title Principal Investigator Name Institution/Department Contact Email

2. Study Summary

Brief Description of the Study

3. Study Purpose and Hypothesis

Purpose of the Study Hypothesis or Research Questions

4. Study Participants

Description of Participant Population Inclusion and Exclusion Criteria Recruitment Methods

5. Study Procedures

Procedures and Data Collection Methods

6. Data Management

How will data be kept confidential? Data Storage and Security Duration of Data Retention

7. Risks and Benefits

Describe Potential Risks to Participants Describe Potential Benefits

8. Informed Consent Process

Describe Process for Obtaining Informed Consent

9. Additional Information

Additional Relevant Information