Informed consent
Chapter 4.2 in the National Statement on Ethical Conduct in Human Research (2023) outlines the ethical concerns for children and young people in research. In most instances, the parent/guardian and the child should provide consent to participate. The HREC will consider and may approve research to which only the young person consents, if it is satisfied that the research is low risk, aims to benefit the participant group, and involves only young people who are able to provide informed consent.
Research with children and young people under 18 years of age raises particular issues around informed consent. Usually, you need to get consent from:
- the child or young person and
- the parent or guardian.
When you are seeking consent from a child or young person, you need to think about:
- their capacity to understand what the research involves and
- the complexity of the research, and its potential risks and benefit.
You should respect the developing capacity of children and young people to be involved in decisions about their participation in research - see Chapter 4.2 in the National Statement on Ethical Conduct in Human Research (2023). In some cases, parental consent may not be necessary. For example, a 17 year-old with good literacy skills may be able to consent to low-risk research.
Justification should be provided to the HREC for the use of young person's consent and which addresses each of the following points:
- (a) Outline how the researchers would make the determination that the young person is mature enough to understand the relevant information and to give consent, although vulnerable because of relative immaturity in other respects;
- (b) whether the research involves no more than low risk (see Chapter 2.1);
- (c) how the research aims to benefit the category of children or young people to which this participant belongs; AND
- (d) either
- 1. the young person is estranged or separated from parents or guardian, and provision is made to protect the young person's safety, security and wellbeing in the conduct of the research (see 4.2.5). (In this case, although the child's circumstances may mean he or she is at some risk, for example because of being homeless, the research itself must still be no more than low risk); or
- 2. it would be contrary to the best interests of the young person to seek consent from the parents, and provision is made to protect the young person's safety, security and wellbeing in the conduct of the research (see 4.2.5)
- 3. If the child cannot consent, you should still involve them in appropriate discussions about the research. Please refer to our Easy read and Parent and Guardian PICFs for guidance.
Name |
Purpose |
Format |
Link |
Participant Information Letter and Consent Form (Parents and Guardians) |
Use this PICF for parents and guardians |
.docx |
Download |
Participant Information Letter (Easy read) |
This is a simple language PIL that can be adapted to suit your audience e.g., for children, or people with an intellectual disability, English as a second language or CALD background. |
.docx |
Download |
Learn more about informed consent