Skip to Main Content

Institutional Review Board (IRB)

Informed Consent

When you’re doing human subject-based research, you are required to obtain informed consent from your participants before you begin collecting their information. 

How do informed consent statements benefit your project?

  • They help the people who might participate in your study make a clear-headed decision about taking on any of the risks that might come with it 
  • They help you, the researcher, reduce the chance of participants underestimating or misinterpreting those risks

Two Parts to Informed Consent

Information
You, the researcher, need to clearly and plainly state what your project is about.

  • What are you studying?
  • Why do you need human subjects to participate, and
  • What are they expected to do?
  • What risks do those participants face?
  • What benefits might they gain?

Consent

Your human subjects need to agree to participate in your study. What that agreement looks like depends on how much risk is involved. 

  • Is your study completely anonymous? If you will collect no information from participants that could identify them, you can simply provide them with your project overview and a statement letting them know that their participation is proof of their consent.
  • If your study is not anonymous – if it is somehow possible to connect your participants’ identities to what they’ve shared with you – you will need to obtain documentation of their consent. But how?
    • You can collect signed paper or fax agreements.
    • You can collect electronic signature agreements.
    • You can record agreements that you receive during a telephone or video call.

What is Privacy?

It’s important to keep your participants’ information private.

But what is privacy? In research, privacy means having control over when, how, and how much personal information human subjects share with others. 

What is Confidentiality?

Confidentiality is an important aspect of human subject-based research.

While privacy, and the risks associated with it, can be discussed with your participants before you begin your project, confidentiality is up to you, the researcher, to maintain after that private data has been collected. 

Remember:
There is always risk involved when you’re doing research with human subjects! Including your plans to maintain confidentiality in your consent statement will help your participants feel reassured about their safety.