Clinical Trial Details
— Status: Recruiting
Administrative data
NCT number |
NCT02753335 |
Other study ID # |
2014/1671(REK) |
Secondary ID |
|
Status |
Recruiting |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
September 2016 |
Est. completion date |
December 2024 |
Study information
Verified date |
May 2023 |
Source |
University of Tromso |
Contact |
Gunnvald Kvarstein, PhD |
Email |
gunnvald.kvarstein[@]uit.no |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
The intention of this trial is to investigate whether combined Graded Motor Imagery (GMI) and
Desensitization (D) among patients with CRPS is clinically more effective than only D and to
study changes in connectivity in the Default Mode Network before and after treatment.
Description:
CRPS: Complex regional pain syndrome (CRPS) is characterized by severe and disabling pain
typically in a limb in combination with sensory, autonomic, trophic, and motor abnormalities
like tremor and dystonia. A distinction is made between CRPS-1, usually following an injury
(fracture, surgery) without a nerve lesion, and CRPS-2, in which a distinct nerve lesion can
be identified.
Brain mapping studies have provided increasing evidence that the central nervous system is
playing an important role in the pathogenesis of CRPS. Reorganization of the somatosensory
cortex and motor networks, with altered central processing of tactile and nociceptive stimuli
as well as movement control has been demonstrated.
Functional brain imaging studies suggest that the volume of brain activation differs between
motor execution and motor imagery, but the distribution of cerebral activity tends to be
similar. Under imaginary movement of affected hands Gieteling et al. (2008) observed that
there was reduced activation ipsilaterally in the premotor and adjacent prefrontal cortex,
frontal operculum, anterior part of the insula cortex, and the superior temporal gyrus.
Stimulus-driven, functional magnetic resonance imaging, however, are time-consuming and prone
to possible confounds, especially in clinical populations. In that perspective resting-state
functional magnetic resonance imaging (RS-fMRI), measuring the cerebral networks at rest (in
absence of any task), is probably better suited to clinical examinations and is widely used
to investigate brain networks that exhibit correlated fluctuations. During recent years, a
large number of studies have indicated that RS-fMRI is sufficiently constrained by anatomy to
allow the architecture of distinct brain systems to be characterized.
The default mode network (DMN) is probably the most studied resting state network. It seems
to be involved in several processes and is found negatively modulated by chronic pain. Only
one published study has investigated cerebral networks and cerebral connectivity in CRPS.
Here the default mode network displayed reduced connectivity with the S1 compared to healthy
controls. This indicates that decreased connectivity may be a key feature in cerebral
functioning of CRPS patients. No study, however, has so far investigated if the reduced
connectivity in the DMN is reversed in CRPS patients who experience pain reduction after GMI
or desensitization treatment.
Diffusion tensor imaging (DTI) is another magnetic resonance technique useful for revealing
microstructural properties of tissue, particularly in cerebral white matter.
Chronic pain has also been associated with reduced cognitive functioning. If this is caused
by pain processing demands, competing with working memory and executive functions, the
investigators would expect the cognitive capacity to be improved or restored if the pain is
successfully treated.
Graded Motor Imagery: Graded Motor Imagery (GMI) is a rehabilitation process and has been
used to treat chronic pain conditions and movement problems related to alterations in the
nervous system such as CRPS, postamputation limb pain, and back pain. The patients are
trained in monitored steps which increase in difficulty as progress is made. The three
treatment components include left/right discrimination training, motor imagery exercises and
mirror observations of the unaffected limb, appearing as the affected limb. The components
are performed sequentially, but require a flexible approach to suit the individual patient.
The imagined movements have been demonstrated to activate motor cortical areas similar to
those activated in the actual execution of that movement.
Desensitization: Tactile desensitization (D) is used to decrease hyperalgesia and allodynia
by repeatedly touching the affected area with various materials. This has successfully been
used clinically in the treatment of CRPS.
Hypotheses: The following hypotheses will be investigated:
1. Patients, treated with GMI + D, experience a larger pain reduction compared with those
subjected to D only.
2. Non-responders to D alone experience pain reduction when D is combined with GMI.
3. Patients with CRPS display reduced intra-network connectivity in the DMN compared to
healthy controls.
4. Reduced intra-network connectivity in CRPS is associated with pain intensity.
5. Reduced connectivity in the DMN is reversed in patients who experience pain reduction
after GMI and D treatment. This will be evident in the comparison of fMRI data obtained
before and after treatment.
6. Microstructure of the cerebral white matter is changed during the intervention.
Design:The effects of treatment with Graded Motor Imagery (GMI ) and D versus D alone will be
compared with an open, randomized, semi-cross-over case-control design.
The study patients will be allocated to either GMI+D or D alone. After an initial treatment
period of six weeks responders (R) stay in the same treatment group and continue this
treatment. Non-responders (NR) in the D treatment group will be offered an immediate combined
treatment (GMI+D).
Randomization: The recruited patients will be allocated in a ratio 1:1 by randomization with
a fixed block size of 6.
Analytical models: Self reported symptom burden and functional capacity will be compared
between the two treatment groups and within each treatment group (i.e. comparisons before and
after treatment and with each patient as his/her own control).
The investigators will also compare the two intervention groups (CRPS patients receiving a
GMI+D and D alone) with a non-randomized comparison group of sex- and age-matched healthy
persons.
Continuous, symmetrically distributed variables will be expressed by mean values with 95%
confidence intervals (95% CI) constructed by the Student procedure. Proportions will be
presented using the Binomial model with the exact 95% calculated confidence interval.
Assumed continuously distributed variables will be analyzed by Analysis of Variance (ANOVA)
model with the initial value as covariate while contingency table analysis is used for group
comparisons of categorical and ranked variables.
The sample size calculation is based on distribution of the main variable, self-rated limb
pain measured by Visual Analogue scaling (VAS). Based on the assumption of normality, a
significance level of 5 % (α = 0.05), a power of (β = 0.80) and a clinical relevant
difference of one time Standard Deviation (SD), 21 patients should be included in each of the
two treatment groups. There will also be a sex- and age-matched comparison group of healthy
persons (n:21).
Interventions:
Individually adjusted Graded motor imagery (GMI) and tactile desensitization (D).
Measurements:
MRI-scanning (for analyses of Intra-network connectivity in the DMN and DTI for
microstructural changes in the white matter), Quantitative Sensory Testing (QST) and
Neuropsychological tests are performed before the randomization and 12 months later.
Self reporting questionnaires will be performed at baseline, after the treatment period of
six weeks, and at the 6 and 12 month follow up.
This includes demographic variables, and a comorbidity check list of diseases related to the
major organ systems, pain intensity measured by numerical scales for pain intensity and by
Visual Analogue Scale (VAS), consumption of analgesics and the questionnaires: CRPS Severity
Score, if upper limb affected; Quick DASH (a short form of Disabilities of the Arm, Shoulder
and Hand Outcome Measure), if lower limb affected; Lower extremity functional scale, Impact
of Event Scale-6 if subjected to adverse life events, Insomnia Severity Index, The Hopkins
Symptoms Checklist (HSCL- 25), Pain Catastrophizing Scale, Perceived self efficacy and the
Bath CRPS Body Perception Disturbance Scale