Complex Regional Pain Syndrome (CRPS) is a debilitating pain condition that usually develops following trauma. Patients with CRPS experience intense, continuing, disproportionate pain and multiple symptoms such as changes or asymmetry in colour, temperature or oedema, as well as stiffness, tremors or dystonia and body perception disturbances. Body perception disturbances are now recognised as part of the typical presentation of CRPS and have been shown to correlate, in particular, with pain intensity. Managing CRPS is challenging and treatment options are limited. Among these, treatments aimed at cortical reorganisation, such as Graded Motor Imagery (GMI), have shown evidence of efficacy in terms of pain and function. However, with regard to body perception disorders, the evidence is limited and emerging. Our aim is to evaluate the effects of Graded Motor Imagery on body perception disorders in patients with upper limb CRPS. Method: a randomised controlled trial comparing an intervention group - therapeutic exercises plus GMI for 6 weeks (implicit motor imagery, explicit motor imagery followed by mirror therapy) - with a control group - therapeutic exercises plus sham-GMI (non-motor mental imagery) for 6 weeks. Outcome measures: body perception disorders (Bath Scale), pain intensity (Numerical Rating Scale), quality of life (PROMIS 29), catastrophising (PCS), fear of pain, CRPS Severity Score, patient-reported global impression of change, medication use and self-efficacy. Interventions are carried out in private practice by independent physiotherapists. Assessors are blinded for the primary outcome. A qualitative component will explore the experiences and perceptions of patients and therapists regarding body perception disturbances, GMI and participation in a research project. This study aims are to improve treatment options for the management of SDRC and to improve the recognition and treatment of body perception disorders in SDRC.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
80
Functional, mobility, strengthening, and mobilization exercises, both passive and active. The exercises are designed to improve mobility and function in the affected limb. In addition to this standard treatment, the intervention group will receive care using Gradual Motor Imagery. The protocol lasts 6 weeks (3 sessions of 15 minutes per day), divided into 3 phases: implicit motor imagery, explicit motor imagery followed by mirror therapy
Functional, mobility, strengthening, and mobilization exercises, both passive and active. The exercises are designed to improve mobility and function in the affected limb. In addition to this standard treatment, the control group will receive a non-motor mental imagery intervention (visual imagery or sham-GMI), designed not to stimulate the sensorimotor areas of the brain while resembling IMG (3 sessions of 15 minutes per day for 6 weeks).
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Body perception disorders (Bath Scale)
Assessment of body perception disturbances; 7 items
Time frame: End of intervention (Week 6)
Body perception disorders (Bath Scale)
Assessment of body perception disturbances; 7 items
Time frame: 3 months after intervention (M3)
Mean pain intensity (Numeric rating scale)
Mean pain during the last week, mean pain during the last week during movement, mean pain during the last week at rest
Time frame: End of intervention (Week 6), 3 months after intervention (M3)
QuickDash
Self-reported assessment of upper limb function :
Time frame: End of intervention (Week 6), 3 months after intervention (M3)
PROMIS 29
Self-reported assessment of quality of life (7 domains, 29 items)
Time frame: End of intervention (Week 6), 3 months after intervention (M3)
Pain Catastrophizing Scale (PCS)
Self-reported assessment of pain catastrophizing
Time frame: End of intervention (Week 6), 3 months after intervention (M3)
Tampa Scale of Kinesiophobia (short form)
Self-reported assessment of fear of movement (6 items)
Time frame: End of intervention (Week 6), 3 months after intervention (M3)
Pain Self Efficacy Questionnaire (PSEQ)
Self-reported assessment of confidence in performing activities despite ongoing pain
Time frame: End of intervention (Week 6), 3 months after intervention (M3)
Patient Global Impression of Change (PGIC)
Self-administered questions asking respondents to rate how their condition has changed since the intervention
Time frame: End of intervention (Week 6), 3 months after intervention (M3)
Medication Quantification Scale (MQS)
MQS quantifies pain medication use and provides a score.
Time frame: End of intervention (Week 6), 3 months after intervention (M3)
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