This page lists research studies that are currently looking for participants from our community. We update it as new opportunities come to our attention, so it’s worth checking back regularly. We also share new studies via our newsletter and social media.
If you have any questions about a study listed here, please contact the research team directly using the details provided — we are not able to answer questions about individual studies on their behalf.
You can find out more about how we support research on our Research page below
Research studies come in many different forms. Some simply ask you to complete a survey or answer questions in an interview about your experience. Others might involve trying a treatment or attending clinic appointments over a longer period. Whatever the study, there are some things you should always expect.
You will be given full information first. Before you agree to take part, the research team should give you a clear explanation of what is involved, usually in the form of a participant information leaflet. Take time to read it and ask any questions you have. You should never feel rushed into a decision.
You will need to give your consent. Consent means actively agreeing to take part, having understood what is involved. For most studies this will be in writing, though some use verbal consent. Consent must be given freely, without pressure from anyone, and you must have the information and capacity to make the decision yourself.
You can withdraw at any time. Taking part in research is always voluntary. If you change your mind before, during or after a study you have the right to withdraw without giving a reason and without it affecting your care in any way.
Your information will be kept private. Research teams are required to handle your personal information securely and in accordance with data protection law. The participant information leaflet for each study should explain how your data will be stored and used.
All research is ethically reviewed. Studies involving people must be approved by a Research Ethics Committee before they can go ahead. This process checks that the research is safe, that the risks are proportionate to the benefits, and that participants will be treated with respect.
For more detail on any of these areas, the NIHR’s Be Part of Research website is a helpful resource.
University of Plymouth
This study is trying to understand why it can be hard for people with PGP to take part in research, and what would make it easier. Researchers want to hear from anyone who has experienced pregnancy-related pelvic pain whether recently or in the past.
Taking part involves a single conversation of around 30 to 45 minutes with researcher Jasmine Darley, by phone, video call or in person. You will be asked about what might make you want to join a research study, what might put you off, and what researchers could do to make participation work better for people with PGP. The conversation is recorded and your information will be kept anonymous.
To take part you need to be 18 or over, living in the UK, and to have experienced pregnancy-related pelvic pain at any point.
Find out more and register your interest
University of Hertfordshire
This study is looking at the relationship between hypermobility and musculoskeletal conditions during and after pregnancy.
For more information or to take part, contact researcher Elizabeth Watson-Rose at e.watson5@herts.ac.uk
