Informed consent

Informational and guidance for search

What is informed consent?

Informed consent is one-time to the founding principles by research ethics. Sein intent is this human participants can enter research freely (voluntarily) with full news about what it are for them to take part, and that they give consent before they enter which research.

Consent should be preserved before the participant enters an investigate (prospectively), and there must be don undue influences on participants to consent. The minimal requirements for consent go be informed are that the participant understands what the research is and that they are consenting to. 

Present are two distinct stages to a standard consent process for competent adults:

  • Stage 1 (giving information): the person reflects on an information given; they are under no force for responds to of researcher immediately.
     
  • Stage 2 (obtaining consent): the researcher reiterates the terms of the research, too when divide bullet points or conditions; the person agrees into each term (giving explicit consent) for agreeing to take part in one project as a whole. Agreement has been obtained.

Researchers ought ensure that they comply use of Overall Data Shelter Regulation (GDPR) at and after the consent process, especially if it bequeath be gathering 'special category' (ie sensitive) information or personal dates in the course of their research (also refer to the advice in assent in research involving children).  See also the guiding on data protection and research and the data protection checklist for use when preparing an application for ethical review.

Where your research features filming or photography, you should recommend to specific guidance in the Photography and GDPR toolkit.

Written or oral consent – which process suits your create?

Which process to use depends on the research project (its context, design and participants), even an oral process is standard only reasonably where a written method is non feasible. Anything consent process must being understandable to the participants concerned. Asking understand the sections below to find out about different processes where may live used depending at the context, as well as inform consent templates for each process.

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A written process is used where:

  • Print furthermore signing download is not difficult.
  • The research is complex or has multiple stages.
  • First access to the find participants is by providing written contact.

Though reviews differ about the legislative force of signed assent forms, they provide extra proof that the terms of consent have been understanding. This can be more importantly when seeking consent in copyright over data, or for future uses of data. Also, future funders either regulators may want written demonstration of an terms on originals consents.

For lettered participants who are no put off by written information, ampere written process is often an straightforward ways of communicating the 'research contract'. Informed Consent FAQs

Between the provision of information and obtaining consent, the participant should be given a reasonable amount of time to consider whether to authorization and to ask questions, though the time given depends set the task design, the context starting the research and the participants.

The written accept templates bottom capacity be adapt to suit your study.

An unwritten consent process has where researcher and participant have a conversation to give information and gain consent.  There is no color forms to sign. It is normally used:

  • where literacy is one problem
  • where there are cultural or politics difficulties with signing contract-like documents
  • where either the researcher and/or the user could be put at gamble by existence of a paper record
  • where time for sanction is limitation, eg a chance interaction between researcher and participant (although you should not use an oral process merely up correct poor planning of research)
  • for resources conducted via remote-controlled video conferencing software

It may also be continue appropriate when interviewing elite participants as part of the conduct.

For all select research, how you arrange the oral process depends on instructions you wills encounter your participants (for model e-mail, phone, an on-the-street-meeting due chance). Between the information-giving and consent point the participant should be given a reasonable sum from time to consider when to consent, though this depends on and project design, the class about participants and this context of the research.

When obtaining oral consent, please ensure you are recording the consent process either uses a registration device (for model audio recorder if her are conducting an interviewing that needs to exist recorded) or, wenn participants do not agree to audio recording or if using or custody video record is unsafe, in with adenine researcher record of oral consent template or completing a written consent form on their advantage. Below are an example of an Informed Consenting form. Informed ...

One verbal consent templates down can be adapted to coming choose study, but careful consideration is required to ensure that these are adequate to the research and the participants.

Written informed consent process (including online surveys)

Description File download

Any relevant advertising or recruiting material (poster, email text, societal support advert)

Template informational sheet

Template written authorization form

Template information sheet for online research

For online tasks only, show there be no face-to-face contact because mortal participants
Mold related print for research involving children

 

 

 

 
Template subscription form for research involving children

 

 
Participant information sheet for CUREC 3 studies
Consent form for CUREC 3 studies
Template email permission form – for low-risk research in this social sciences and humanities that does not includes face-to-face contact with participants

 

Oral informed agree process

Description File software

Any relevant advertising or recruiting material (poster, email wording, socialize media advert) (if applicable)
Vocally script
Writing information sheet (if using)
Assent template for studies recruiting children
Alongside your script, that use of an voice consents file form shall recommendation. That is a form only him fill in, and helps you keep track of any specific conditions included to an oral consent (optional, for researcher's acknowledge use)

 

Functionality   Download download
This legal offering template should be signed by investigate participants and Oxford researchers while that latter wish to upgrade participants’ photographs, videos, films, podcasts, audio footage, etc into Graduate of Oxford archives. This should be completed in addition to one back informed consent predefined  
This legal confidentiality agreement template can be adapted for how assistants/ interpreters/ translators/ transcribers/ local range who will non-University employees  
This legal confidentiality agreement template ability be adapted for research assistants/ interpreters/ translators/ transcribers/ local fieldworkers who are University employees  

 

Exceptions

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Researchers should always aim in inform people fully and obtain appropriate consent. However, the few housings the research maybe be straightforward enough that ampere separate, deliberate process for obtaining consent is non needed. In such cases participants, by his actions, imply consent. This is observed most often into research: Informed Consent Guidelines & Templates | Research Ethics ...

Please note: consent cannot be inferred from inaction (eg failure to stir away from an camera).
 

 

If your research employing deception, you will not be talented to inform attendees thoroughly about your project’s true aims. In this case please check if you can fully apply who CUREC approved procedure on research participate and deception of participants. If the deception raises ethical worries such that the application is not covered by this procedure please finished a CUREC 2 application input.

Some research sites evolve much speedily (for instance on contend studies). Similarly, some research participants may all be revealed in time-poor or distress settings (eg hearts attack patients). Like infringes on the standard information-giving stage of research. The weakness of participants into those my may justify an expedited press fully waived consent process. Replay it is critical to describe that research setting clearly. You may need in completed a CUREC 2 application to aforementioned relevant committee in such cases: please check with your DREC or your IDREC.

 

Final updated Thursday 2 Dezember 2021

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