Lead Sponsor

Centre Hospitalier Universitaire de Nīmes

Age

18 - 70 years

Sex

ALL

Healthy Volunteers

No

•The patient must have given their free and informed consent and signed the consent form
•The patient must be a member or beneficiary of a health insurance plan
•Patient with CRPS of the upper limb according to the Budapest criteria.
•Patient newly treated at the Centre d'Evaluation et de Traitement de la Douleur of the CHU of Nîmes.
•Patient with a diagnosis of CRPS for more than 3 months

•The subject is participating in a therapeutic study, or is in a period of exclusion determined by a previous study
•The subject unable to express consent
•It is impossible to give the subject informed information
•The patient is under safeguard of justice or state guardianship
•Patient is pregnant, parturient or breastfeeding
•Patient with medically significant visual impairment that is incompatible with the practice of ARMT
•Patient with CRPS secondary to a stroke
•Patient with cognitive disorders (Montreal Cognitive Assessment scale less than 26)
•Patient with Unilateral Spatial Negligence according to the Bell's test
•Patient with arthrodesis of one of the joints of the upper limbs.
•Patient with an unhealed fracture of one of the upper limbs