Complex Regional Pain Syndrome (CRPS)
Conditions
Keywords
Transcranial direct current stimulation, Complex Regional Pain Syndrome, pain, quality of life, anxiety, central sensitization
Brief summary
Transcranial direct current stimulation (tDCS) is a non-invasive therapy increasingly used in facilities treating patients with chronic pain. This complementary therapy has the advantage of being non-pharmacological, with transient and mild side effects, an excellent safety profile, and good efficacy in the contexts where it has been the subject of dedicated research: neuropathic pain, fibromyalgia, and visceral pain. Few studies have focused on the application of tDCS in the context of complex regional pain syndrome (CRPS), which is a common condition.
Detailed description
This protocol aims to compare a group receiving a tDCS protocol with a sham control group. The hypothesis of this study is that tDCS is effective in treating CRPS in terms of reducing pain and the functional and emotional consequences of pain. The primary objective of the study is to evaluate the effectiveness of tDCS on pain in patients with CRPS (complex regional pain syndrome), measured by the numerical pain scale (EN), after one month of treatment and one month after the end of treatment, compared to the sham arm. The secondary objectives are: * To assess anxiety and depression symptoms (HAD) * To assess the functional impact of pain (Concise Pain Questionnaire - QCD) * To assess central sensitization (Central Sensitization Inventory - CSI) * To identify adverse effects related to tDCS
Interventions
OTHERtranscranial direct current stimulation
progressive increase in stimulation intensity up to 2 mA, then continuation at a plateau for a total of 20 minutes, then a decrease in stimulation intensity for 30 seconds at the end of the session before an automatic stop.
OTHERPlacebo
The stimulation intensity is gradually increased up to 2 mA for 1 minute, then decreased to zero stimulation. A further increase in stimulation is programmed 10 minutes after the start of stimulation.
Sponsors
Polyclinique de l'Europe
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Major * Clinically active or active complex regional pain syndrome (CRPS) with positive Budapest criteria * Scintigraphy showing signs consistent with CRPS * Being affiliated with or a beneficiary of a social security scheme
Exclusion criteria
* Algodystrophy no longer meeting the Budapest criteria * Relative contraindication to tDCS: psychosis (including treated psychosis), uncontrolled epilepsy, large scalp scar, intracerebral/intracranial metallic body * Pregnant or breastfeeding women * Minors * Persons under legal protection (guardianship, conservatorship, and protective supervision) * Persons deprived of their liberty by judicial or administrative order * Unwilling individuals who cannot give their consent or cannot return for scheduled visits according to the protocol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Analog Visual Scale | one month post treatment |
Countries
France
Contacts
CONTACTValentin Billard
Outcome results
None listed