Status:
COMPLETED
The Complex Regional Pain Syndrome (CRPS) is a Chronic Pain Condition. This is a Preliminary Study to Explore and Test Clinical Hypothesis. They Suppose That CRPS Patients Have Impairment in Their Mental or Motor Imagery Abilities.
Lead Sponsor:
Centre Hospitalier Universitaire de Nīmes
Conditions:
Complex Regional Pain Syndromes
Musculoskeletal Pain Disorder
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Medical functional imagery seems to demonstrate that patients suffering from complex regional pain syndrome (CRPS) have cortical modifications that alter their motor (or mental) imagery capacities. No...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- Patient with French healthcare affiliation
- Adult patient (\> 18 years old)
- Patient with bachelor degree minimum
- Patient practicing less than 150 minutes of moderate to intense physical activity per week
- Specific Inclusion Criteria for CRPS group :
- Patient followed in the Evaluation and Treatment pain center (University Hospital of Nimes)
- Patient with secondary CRPS due to a traumatism or a surgery
- Specific Inclusion Criteria for Musculoskeletal group :
- Patient with musculoskelettal disorder on a limb (upper or lower)
- Patient followed in the University Hospital of Nimes
- Non inclusion Criteria :
- Patient who participates in another category 1 research
- Patient in a exclusion period in another study
- Patient under legal protection, under guardianship or under curatorship
- Patient for whom it is impossible to give clear information.
- Pregnant, parturient or breastfeeding patient.
- Patient with amputation on one of his limb
- Patient with visual cecity
- Patient who has already practiced mental imagery
- Patient with neurological impairment
- Patient with chronic low back pain and fibromyalgia
- Specific non inclusion criteria for Musculoskeletal group and healthy group :
- Patient with CRPS
- Specific non inclusion Criteria for CRPS group :
- Secondary CRPS to CVA (cerebrovascular accident)
- Patient receiving lymph node block treatment between the inclusion visit and the follow-up visit
- Specific non inclusion Criteria for Musculoskeletal Disorder group :
- Patient with secondary musculoskeletal disorder to a CVA
- Exclusion criteria :
- Questionnaire MIQ-RS not completed or non respect with the research protocol
- pathology discovered incompatible with the study criteria
Exclusion
Key Trial Info
Start Date :
January 12 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 30 2022
Estimated Enrollment :
129 Patients enrolled
Trial Details
Trial ID
NCT04703348
Start Date
January 12 2021
End Date
October 30 2022
Last Update
December 4 2025
Active Locations (1)
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1
CHU de Nimes
Nîmes, Gard, France, 30029 NIMES Cedex 9