Benefit of Augmented Reality Mirror Therapy in Addition to Conventional Management in Complex Regional Pain Syndrome of the Upper Extremity

Centre Hospitalier Universitaire de Nīmes7 enrolled

Overview

Complex Regional Pain Syndrome (CRPS) is a "polymorphic joint and periarticular pain syndrome associated with various changes in sensitivity, vasomotor, sudomotor, muscular and trophic changes". The diagnostic criteria of the disease follow the Budapest criteria, namely (i) vasomotor disorders (temperature asymmetry, color changes), (ii) sudomotor/oedema (sweating changes, edema), (iii) sensory (hyperesthesia, allodynia, hyperalgesia) and (iv) motor/trophic (reduced joint mobility, weakness, tremor, dystonia, trophic disorders of skin, nails, hair). Of the many treatments, augmented reality mirror therapy (ARMT), is novel in substituting a virtual environment for part of the real environment. This type of device has never been studied from a clinical point of view in the treatment of upper limb CRPS, whereas fMRI and clinical dissertation studies have suggested an improvement in neuroplasticity. The aim of this study is to establish the clinical effects of ARMT on CRPS, and to evaluate its benefit within a conventional rehabilitation treatment (physiotherapy and occupational therapy).

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

OTHER

Masking

SINGLE

Enrollment

Conditions

Complex Regional Pain Syndromes

Interventions

Conventional therapyOTHER

The CT consists of 1 session of 30 minutes of physical therapy (type of re-education established according to the pain at rest and during movement assessed every day) and 1 session of 30 minutes of occupational therapy (type of re-education established according to the pain at rest and during movement assessed every day). CT is performed 5 days a week.

cortical reactivityOTHER

An electroencephalogram was taken at the start and end of the study to study cortical reactivity during the performance of 3 different tasks repeated 30 times: a resting task (consisting of looking at a cross on a screen), a motor imagery task (consisting of imagining performing wrist flexions/extensions) and a motor execution task (consisting of performing wrist flexions/extensions).

Eligibility

Sex: ALLMin age: 18 YearsMax age: 70 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 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 Exclusion Criteria: * 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

Outcomes

Primary Outcomes

Improvement in upper extremity motor function using ARMT versus CT alone

Change in Box and Block Test (BBT) score. The score will be compared between the right and left hand and against reference values according to age and sex.