If you are ever considering taking part in a clinical trial, always make sure:
- you understand what the trial is about, why you are being asked to take part and what you will need to do if you do consent to take part;
- you have been informed of and considered the risks and benefits of taking part, and how your rights, data and identity will be protected;
- you are able to comply with the tasks required of you, and can make the time commitment to attend all visits;
- that the study has been approved by a recognised research ethics committee, and you know how to contact them if you have questions or problems with the research/research team (this information should be available in the participant information provided to you prior to consent);
- you know that it is OK to say no to taking part, and that you must consent before a researcher conducts any tests;
- that you can ask questions at any time if you have them ;
- you don’t assume that you will always do better by participating in the clinical trial;
- that if you agree to take part, you can withdraw at any time, without consequence to your relationship with the research team or ongoing care;
- that you know what will happen at the end of the trial with your ongoing care, and whether you will receive a summary of the trial findings or data;
- you know who to contact if you have questions or need help.
If you are ever unsure about anything clinical trial related, and the knowledge base doesn’t help you, please get in touch.