MultiSENSory Stimulation to TArgeT Sensory Loss and ChronIc Pain in NeurOpathic PatieNts
NCT ID: NCT05483816
Last Updated: 2024-11-18
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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RECRUITING
NA
40 participants
INTERVENTIONAL
2022-06-30
2028-02-28
Brief Summary
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Today, proper treatments for neuropathic pain that exclude pharmacological solutions are still missing. This is due to the complexity of the neurobiological mechanisms underlying the origin of neuropathy, the multifaceted physical and psychological nature of pain and the lack of reliable biomarkers.
The aim of this project is to tackle the major problems connected to neuropathy thanks to non-invasive stimulation of the peripheral nervous system. The system is composed of an insole with pressure sensors that captures in real time the force exerted by the subject on the foot and couples this information with parameters of electrical stimulation. Thanks to optimal electrode placement and intensity modulation, subjects are able to perceive in real-time in a somatotopic manner (i.e., under their foot) how they are walking. The aim now is twofold: first the investigators want to couple this stimulation with Virtual Reality (VR) to develop a neuroadaptive non-invasive brain computer interface (BCI) to treat pain and secondly the investigators want to measure through fMRI scans whether the use of the sensory feedback system allows any beneficial plastic changes in the brain. Finally, the investigators want to measure through fMRI scans whether the use of the sensory feedback system allows any beneficial plastic changes in the brain.
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Detailed Description
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The reasons of such lack of efficacy can be attributed to different factors, among which the lack of therapies addressing the multidimensions of pain, as pain is not a unitary phenomenon, rather a multidimensional outcome of sensory-discriminative and motivational-affective components, that should be synergistically accounted for, and the lack of reliable biomarkers: objective indicators of pain are needed to demonstrate therapeutic target engagement, to stratify patients and to predict disease progression or therapeutic responses.
These factors are the main focuses of this study, whose aim is to develop a multisensory platform for pain, detecting pain through physiological recordings and delivering a therapy when such physiological biomarkers are detected. First the detection of pain is exploited through electrophysiology and then the therapy is delivered by means of Virtual Reality (VR) and Transcutaneous Electrical Nerve Stimulation (TENS), in order to target both physiological and affective/cognitive components of neuropathic pain. VR and TENS have already singularly produced encouraging results in literature\[26-29\]. However, these results are conflicting and not conclusive. The investigators believe that the combination of these technologies, which targets all the different aspects of pain, will really provide a successful and lasting benefit to the patients chronic pain.
Furthermore, the nature of the platform, which includes the use of non-invasive electrical stimulation, allows to recreate sensations in parts of the body where the subjects don't feel sensations anymore. Indeed, thanks to years of research, the Neuro-engineering laboratory found optimal stimulation parameters and electrode placement which are able to elicit sensations far from the electrodes placement. Electrodes are indeed placed on healthy parts of the nerves, but the perceived sensation is in the extremities. This allows to target also another extremely common consequence of neuropathy: sensory loss. This symptom forces patients to have an altered gait strategy, impaired balance and a five-fold increased risk of falling. Therefore, in this study the investigators will monitor also the potential benefits of the platform on these aspects.
As for the imaging sessions, before starting the imaging sessions, patients will be assessed to obtain potential information that might impact on the results.
Healthy participants and patients will be asked to participate in two-three fMRI sessions. Prior to the scanning, a calibration procedure will take place, to understand the subject's stimulation parameters and characterize the location and type of sensations elicited.
During the fMRI sessions, the investigators will examine the neural correlates of the referred perceptions and any pain relief induced using the non-invasive TENS stimulation approach. During these sessions different types of stimulations will be performed (with the TENS stimulation system, with vibrotactile stimulators, and with visual stimulations). Resting state fMRI will be used to examine functional connectivity between different regions of interest. Each fMRI session will last \~70-80 minutes.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Virtual Reality and Transcutaneous Electrical Nerve Stimulation
for healthy subjects: painful stimulus induction (electrical stimulation) for patients: focus/non focus on pain
Therapy is released in presence of pain
VR+TENS
The subjects will receive a therapy that combines electrical pleasant stimulation of the nerves, synchronised with event in virtual reality
Virtual Reality only
only VR delivers therapy
VR+TENS
The subjects will receive a therapy that combines electrical pleasant stimulation of the nerves, synchronised with event in virtual reality
Interventions
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VR+TENS
The subjects will receive a therapy that combines electrical pleasant stimulation of the nerves, synchronised with event in virtual reality
Eligibility Criteria
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Inclusion Criteria
* Visual acuity\>6 on Snellen visual acuity chart
* Exclusion:
* Pregnancy
* Cognitive deficits (Mini Mental State Examination\<23)
* Cyber-sickness
* Prior or current psychological diseases
* Pacemakers
* Epilepsy
* Claustrophobia
* Other MRI contraindications
* Unhealed fractures
* Unhealed wounds
* Cancerous growth in proximity to feet
* Swollen, infected or inflamed areas on feet or skin eruptions on feet such as phlebitis, thrombophlebitis or varicose veins
for patients:
* Inclusion:
* Age 18-80
* Visual acuity\>6 on Snellen visual acuity chart
* Diagnosis of peripheral neuropathy
* Pain in lower limbs\>=3 cm on VAS scale
* Exclusion:
* Pregnancy
* Relevant comorbidities that would affect the outcomes of the study (by judgement of physicians)
* Ulcers
* Cognitive deficits (Mini Mental State Examination\<23)
* Cyber-sickness
* Prior or current psychological diseases
* Pacemakers
* Epilepsy
* Claustrophobia
* Other MRI contraindications
* Unhealed fractures
* Unhealed wounds
* Cancerous growth in proximity to feet
18 Years
80 Years
ALL
Yes
Sponsors
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Neural Control of Movement laboratory ETH Zurich
UNKNOWN
ETH Zurich
OTHER
Responsible Party
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Stanisa Raspopovic
Prof. Dr. Stanisa Raspopovic
Principal Investigators
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Stanisa Raspopovic, Prof. Dr.
Role: PRINCIPAL_INVESTIGATOR
ETH Zurich
Locations
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ETH Zurich
Zurich, Canton of Zurich, Switzerland
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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NeuroengLab
Identifier Type: -
Identifier Source: org_study_id
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