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.

Launched by CENTRE HOSPITALIER UNIVERSITAIRE DE NĪMES · Jan 7, 2021

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Gender

ALL

Eligibility criteria

• 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