Efficacy and Safety of a Learning Program of Self- Rehabilitation Exercises by Mirror Therapy
- Conditions
- Reflex Sympathetic DystrophyCausalgia
- Interventions
- Behavioral: Mirror therapyBehavioral: Usual care
- Registration Number
- NCT02667717
- Brief Summary
AlgoMIR project born thanks to a meeting between pain professionals and re-education staff. The goal of this project is to develop and evaluate a program of learning with exercises by mirror therapy, that could be easily shared with paramedic teams and easily adapted to different handicaps.
Researchers have chosen to select patients with re-education of the upper extremity to benefit from rehabilitation sessions either from physiotherapists present in their city, or of functional rehabilitation hospital units.
- Detailed Description
The Complex Regional Painful Syndromes (CRPS) called in the past aglodystrophia, are characterized by the apparition of pain abnormally spread and intensive compared to the initial causal factor. They are usually associated to negligence of the painful limb, and avoidance movements that require care in rehabilitation that it is carried out in the physiotherapist center or functional rehabilitation unit at hospital.
Recently, mirror therapy has been proposed to correct dysfunctions : patients have to realize a movement with their two hands, observing the reflect of their healthy hand in a mirror, while their painful hand is hidden behind the mirror. After a learning phase, patients have to continue this kind of therapy independently.
AlgoMIR project born thanks to a meeting between pain professionals and re-education staff. The goal of this project is to develop and evaluate a program of learning with exercises by mirror therapy, that could be easily shared with paramedic teams and easily adapted to different handicaps.
Researchers have chosen to select patients with re-education of the upper extremity to benefit from rehabilitation sessions either from physiotherapists present in their city, or of functional rehabilitation hospital units.
The primary outcome of this project is to compare analgesic effect at 8 and 16 weeks of a therapy mirror re-education program associated to a usual care (M+R), and of a usual care program (R).
A second goal is to understand eventual difficulties met by the patients and improve efficacy of the autonomous becoming of patients using mirror therapy.
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 34
- Affiliation to Social Security
- CRPS (complex regional pain syndrome) type I or II defined by the criteria of Bruehl (Table 1)
- CRPS of the upper limb including the wrist and / or hand
- CRPS post-surgical or post-traumatic
- Average pain in the last 24 hours of intensity > = 30/100 on EVA (0 no pain, 100: worst pain imaginable )
- Evolution for over 3 months and less than 2 years
- Patients taking a stable background therapy for 15 days and not having received the following treatments in the previous months : bisphosphonate cure, infiltration, Qutenza, ketamine infusions
- Patients accepting a rehabilitation (physiotherapists or hospital units for patients included on Saint-Etienne and hospital units for patients included in Lyon and Saint- Vallier)
- CRPS post stroke or drug
- Adhesive capsulitis isolated
- Cognitive or language difficulties preventing understanding instructions and / or a correct clinical evaluation
- Patient who already received a rehabilitation program with the use of mirror therapy or other virtual reality technology
- CRPS in connection with an accident caused by a third party for which a legal procedure is underway
- Major Depressive Episode
- Dissociative Disorders
- Visually impaired patients
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Experimental group : Mirror Therapy Usual care Experimental group will perform mirror therapies during 16 weeks, added to the usual care. Therapy mirror sessions will take place at hospital units but also at home. Experimental group : Mirror Therapy Mirror therapy Experimental group will perform mirror therapies during 16 weeks, added to the usual care. Therapy mirror sessions will take place at hospital units but also at home. Control group : Usual care Usual care The control group will benefit from the usual care during 16 weeks. No mirror therapies will be performed to this group.
- Primary Outcome Measures
Name Time Method Compare the Visual Analogue Scale (EVA) of pain Week 8 Compare after 8 weeks the score of EVA of pain in the last 24 hours for patients who performed during 8 weeks :
* a program of mirror therapy associated with the usual care (M+R) or
* the usual care without mirror therapy
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (5)
MPR des Massues
🇫🇷Lyon, France
MPR de l'Hôpital Drôme Nord
🇫🇷Saint Vallier, France
Centre médical de l'Argentière
🇫🇷St Etienne, France
Consultation Douleur de la Mutualité de la Loire
🇫🇷Saint Etienne, France
Chu Saint Etienne
🇫🇷St Etienne, France