Step 6: Obtaining Ethical & Trust Approval

Ethical practice in research is about doing what is possible while protecting stakeholders and research participants. In practical terms this means ensuring your research participants are not exposed to risk as part of your project, protecting their right to anonymity and confidentiality, and that your project has merit. If you’re planning to replicate a previous study, merit relates to whether there is justification in revisiting the research idea, perhaps by applying the research process to a new setting.

Research Governance

Research governance seeks to improve research quality and safeguard the public within the NHS. Research governance involves promoting good practice and enhancing ethical and scientific quality. Whether or not you need to apply for full ethical approval, you’ll need to negotiate with research governance at the NHS sites where you’re conducting the research. More information on NHS research governance and how it might affect your study can be found at:

Research Ethics Frameworks

There are many research ethics frameworks available but for a basic check of the kind of things they cover you can take a look at the Economic and Social Research Council Framework for Research Ethics. In summary, their six key principles of ethical research are:

  • Research should aim to maximise benefit for individuals and society and minimise risk and harm
  • The rights and dignity of individuals and groups should be respected
  • Wherever possible, participation should be voluntary and appropriately informed
  • Research should be conducted with integrity and transparency
  • Lines of responsibility and accountability should be clearly defined
  • Independence of research should be maintained and where conflicts of interest cannot be avoided they should be made explicit

Informed Participants and Seeking Consent

You will need to prepare an information leaflet, sometimes called a participant information sheet, to invite people to take part in your research project. The purpose of the information leaflet is explain what taking part in your research will involve so that people can make an informed decision about whether to contribute to your research.

To ensure your information leaflet is comprehensible you’ll want to check its readability score, a number which tells you how easy it is for someone to read your text. The score is calculated based on the average length of sentences and the length of the words you’ve used. The higher the readability score, the easier your text is to read. It’s generally recommended that information leaflets should aim for a score of 60 or above. If you are using Word to produce your information sheet, you can quickly check the readability score of your text under the Review section’s Check Accessibility.

Informed consent is usually demonstrated by the research participant first reading your information sheet and then either completing and returning your questionnaire, which implies consent, or signing your informed consent form. The following resources will help you prepare your information leaflet and obtain informed consent:

As part of collecting and collating your data (Step 7), signed informed consent forms should be stored in a locked cabinet or on a password protected computer.

Applying for Ethical Approval

Your research proposal (Step 5), including copies of your information sheet and informed consent form, will need to be submitted to your Trust ethics committee for approval. Depending on your study design you may also need to apply for ethical approval at a full regional research ethics council meeting.

The Health Research Authority’s Research Ethics Service (RES) convenes regional Research Ethics Councils (REC), to support and enable ethical research in the NHS. In line with INVOLVE guidance on public involvement, all RECs include five ‘lay’ members who are do not professional interest in research and are not registered healthcare professional. RECs aim to give a decision on research applications within 40 days, though it can sometimes take longer; this time needs to be planned for when you are designing your study (Step 3).

You can get support in ensuring your proposal is ethical from:

You should not begin collecting data until you have received ethical approval.

Suggested Reading

  • Buchanan, E., & Ferguson, S. (2013). Ethics and best practice. In M. J. Grant, B. Sen, & H. Spring (Eds.), Research, evaluation and audit: key steps in demonstrating your value (pp. 65-76). London: Facet Publishing. Provides an overview of why ethics are important, outlining ethical issues in participant selection and consent, anonymity and confidentiality, data storage, informed consent and participant information sheets.
  • Pickard, A. J. (2013). Ethics in research. In A. J. Pickard (Ed.), Research methods in information (2nd ed.). London: Facet Publishing. An accessible account of how to identify potential ethical issues in your research.

Next Steps

Now that you have received ethical approval you can start collecting and collating your data (Step 7).