RecruitingNot ApplicableNCT05483816

MultiSENSory Stimulation to TArgeT Sensory Loss and ChronIc Pain in NeurOpathic PatieNts


Sponsor

ETH Zurich

Enrollment

40 participants

Start Date

Jun 30, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Neuropathy is a costly and disabling health issue, which consists of a degeneration of the peripheral nerves. Even though the causes may be different, such as diabetes or amputation, the consequences for neuropathic patients are multiple and extremely debilitating. Among the alarming symptoms it implicates, chronic pain and sensory loss are among the most severe ones. Because of the loss of sensations, patients are forced to have an altered gait strategy, an impaired balance and a fivefold increased risk of falling. Furthermore, since they lose sensations and feel numbness in their extremity, they are discouraged in walking, hence leading to a sedentary lifestyle. All of this is worsened by the development of neuropathic pain, which has a high comorbidity with psychological issues, such as depression and anxiety. 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.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria7

  • for healthy:
  • Age 18-80
  • Visual acuity\>6 on Snellen visual acuity chart
  • 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 Criteria26

  • 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:
  • 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

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Interventions

COMBINATION_PRODUCTVR+TENS

The subjects will receive a therapy that combines electrical pleasant stimulation of the nerves, synchronised with event in virtual reality


Locations(1)

ETH Zurich

Zurich, Canton of Zurich, Switzerland

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NCT05483816


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