£
We use cookies to improve your experience. By accepting you agree to our cookie policy
The Complex Regional Pain Syndrome (CRPS) and Chronic Pain Research Study Trials Tracker was designed to bring together details of any CRPS and chronic pain trials currently recruiting in the UK. This will enable you to find RCT clinical trials and research studies that you might be eligible to take part, both local to you or further afield.
If you have any questions about taking part in research studies or clinical trials, you can contact us or get in touch with the clinical trial or research study team directly (contact details are included in the opportunity's listing).
If you are a researcher and you would like to include your research study or clinical trial, please send the details by email.
Study recruiting UK-based participants to complete a short survey (5 mins) about things that might make it harder, and things that might make it easier, to take part in chronic pain research.
This study aims to develop clinical recommendations that will expecite patient access to therapy-led treatment across the CRPS care pathway. Participation will involve an online workshop to discuss experiences of therapies received and any changes noticed as a result of receiving this care.
Are you a parent, whose child has been living with Complex Regional Pain Syndrome (CRPS) for more than twelve months? Are you available for a maximum of 1 hour to take part in an online interview? If you can answer yes to these questions, you are invited to take part in a research project to find out if having a child with CRPS impacts the occupational balance of their parents.
Researchers are looking for adults with chronic pain to participate in the study and complete an Internet-based psychological intervention. Participants get permanent access to the intervention.
We want to understand what it is like to live with CRPS. This study will look specifically at how sleep, pain, and doing the activities that are important to a person can impact living with CRPS. There is not much research on sleep in CRPS. We think sleep, pain, and activity levels might work together to make things better or worse. If we can show the importance of sleep to understand the overall life experience of people with CRPS, doctors and therapists may ask about sleep more. It may also help us to develop new ways of improving sleep in people with CRPS.
We use cookies to improve your experience. By accepting you agree to our cookie policy