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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.
Participate in a research study about how chronic pain can affect the perception of facially expressed emotions. This is an online study that you can take part in from your computer and will take no more than 30 minutes.
Study examining the relationship between parental responses, pain catastrophizing and the coping strategies used by the child with chronic pain, the findings of which will add to the limited literature on childhood chronic pain coping from the perspectives of both parents and children. This study will aim to gather a general overview of the different responses used by parents/carers in the UK in their child’s pain management.
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.
Seeking participants for a survey on employer support for employees with chronic pain. Join the survey to contribute to research shaping better workplace wellness policies and practices.
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.
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