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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.
Research exploring what it is like to use antidepressants for managing your pain.
This research is looking at opioid information, and opioid decision making in those with CRPS. Since April 2021, guidelines around opioid use have changed, but how are individuals with CRPS navigating and understanding the information? And are they able to make fully informed decisions about their opioid use? If you have experience in this area and meet the participant criteria, please get in contact.
Respondents are being asked to participate in a research study evaluating the effectiveness of various treatments on chronic pain due to complex regional pain syndrome (CRPS). The short survey is anonymous and confidential, and should take approximately five minutes to complete. The questions will focus on the modalities used to manage chronic pain due to CRPS and will include a Likert scale to rate pain levels after using these interventions.
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.
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.
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