Rehabilitation Protocol for Disorders on Hand Sensitivity in Multiple Sclerosis Patients.
NCT ID: NCT01866878
Last Updated: 2025-12-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
10 participants
INTERVENTIONAL
2013-07-30
2015-07-28
Brief Summary
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A functional impairment based on sensory disorders of the hand. The hand is a sensory organ that transmits the cerebral cortex protopathic sensitive information, proprioceptive or epicritiques. The view-hand association plays an important role in the understanding of the environment. Its exploratory use remains an essential and voluntary basis. The process of recognition of the object passes through manipulation, but operates instantaneously. The brain is able to do a quick summary of the information it receives to determine the nature of the manipulated object. The exploration takes a posteriori, the brain can then determine the details component object (texture, shape, composition, temperature and weight).
Neurophysiological mechanisms that would explain the analgesic effects of transcutaneous electrical nerve stimulation (TENS) are not fully understood. Several theories underlying its use as a neuromodulator of pain. The gate control theory has led to the development of TENS devices. Recruitment of myelinated, large caliber, by the TENS electrodes afferent fibers increases the control exerted on spinal level, thereby inhibiting the action of afferent fibers of small caliber related to nociception. This stimulation strengthens the blocking of "gate" at the corresponding cell bodies of spinothalamic tract and reduces the transmission of nociceptive impulses to the spinal cord dorsal horn. This is segmental presynaptic inhibition depends on the area and stimulated.
The objective of this study is to improve the quality of life through improved sensitivity disorders of the hand in patients with MS, thanks to reeducation of the hand.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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A group enjoying a corrective touch
At first, the patient is asked to gradually define the different types of touch that is applied to the hyposensitive area (fixed or mobile touches) with different textures and then compare them with the healthy side. In a second step, the patient is asked to associate multiple items sensation shape and texture, shape and weight. In a third step is used everyday objects.
Desensitisation techniques find their interest mainly when symptoms or dysesthetic hyperesthésique. The objective is to increase the threshold of sensitivity to textures and particles eventually reduce dysaesthetic sensations.
The patient class in order of increasing tolerance 10 textures. Dysesthetic area is stimulated 5 to 10 minutes by the first texture to numb the area by saturation of the action potential. This helps promote functional work and recognition of objects. As soon as the texture causes more trouble we go to the next texture by applying the same job.
equipment rehabilitation stereognosis
A group receiving TENS (TENS)
Well known in the management of neuropathic pain based on the gate control theory, the application of TENS in the rehabilitation of touch remains to be demonstrated. A recent study applied to the September highlighted the long-term interest of the transcutaneous electrical nerve stimulation (TENS) to improve sensitivity tact arguing possible action on brain plasticity.
TENS
A control group
No interventions assigned to this group
Interventions
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equipment rehabilitation stereognosis
TENS
Eligibility Criteria
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Inclusion Criteria
* Age ≥ 18 years, male or female sex
* Patients with sensory disorders interesting hands, evidenced by clinical examination objective.
* Patients with an EDSS between 2 and 4 with functional sensitivity parameter ≥ 2.
* Patients affiliated to a social security scheme.
* Patients signed informed consent for the study.
Exclusion Criteria
* Patients with allodynia in the study area
* Patients with a motor and / or deficit cerebellar ataxia of the upper limbs.
* Patients treated with psychotropic or antiepileptic drugs.
* Patients for whom a flare occurred affecting the sensitivity of the hand, within 30 days before enrollment.
* Patients holders of an active implantable medical device.
* Pregnant women and vulnerable patient population.
18 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de Nice
OTHER
Responsible Party
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Principal Investigators
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Mikael COHEN, Medical Doctor
Role: STUDY_DIRECTOR
Centre Hospitalier Universitaire de Nice
Locations
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Hôpital Pasteur
Nice, , France
Countries
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Other Identifiers
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12-PP-13
Identifier Type: -
Identifier Source: org_study_id
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