Module 1
- Overview
- Introduction
- Process
- Basic Principles
- Brief History
- What Research Must be Reviewed
- IRB Review Criteria
Module 2
- Overview
- Introduction
- Selecting Participants
- Describing Research
- Discussing Participation
- Ensuring Readability
- Assessing Understanding
Module 3
- Overview
- Continuing Review
- Unanticipated
Developments

- Adverse Events
- Consent Doc. Revisions
Module 4
- Student Test
- Faculty/Staff Test
Helpful Links
- NIH Protecting Human
Participants

- Office for Protection


JMU OSP

Module 2
Discussing Participation

Informed consent involves educating prospective participants, not merely disclosing information. Providing information is part of the process. The essential elements to be conveyed are discussed in the previous section, "Describing the Research." Discussions with prospective participants should take place with sufficient time for them to consider participation. Approaching them on the same day as the study would take place may not be sufficient. Participants may need time to think about their decision or to discuss their involvement with family, friends, or religious advisors. For best results, participants should be approached when they are willing to listen, and are open and ready to consider consenting.

The process of obtaining consent should include time for both discussion and reflection, as shown in the following steps:

Continue to Ensuring Readability -->

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Last Modified July 3, 2008

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