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NCT06218563Completed

Study of Cerebral Activation by fNIRS During Vibration-induced Illusion of Movement in Healthy and Stroke Participants.

Vibration-induced Movement Illusion Causes Cerebral Haemodynamic Changes: A fNIRS Study.

Source: ClinicalTrials.gov · Last updated 8 Jul 2025

Brief summary (registry, in English)

The purpose of this study is to investigate the cerebral activation of healthy and stroke participants in 4 or 2 different conditions (repeated 2 times) of vibration-induced illusion of movement respectively, resulting in 8 or 4 vibration blocks with 3 vibrations per block. The frequency of the vibration being 80 Hz. Healthy participants: * Right arm, eyes opened * Right arm, eyes closed * Left arm, eyes opened * Left arm, eyes closed Stroke participants: * Deficient side, eyes opened * Deficient side, eyes closed The aim is to compare the subjective sensation of movement score and cerebral activations of healthy/stroke participants depending on the condition.

Status (registry)
Completed
Study type
Interventional
Enrollment
90 (actual)
First submitted
12 Jan 2024
Start date
10 Jan 2024
Primary completion date
25 Jun 2025
Lead sponsor
Centre Hospitalier Régional d'Orléans
Diseases
Stroke
NCT number
NCT06218563

What you commit to

  • Study type: Interventional
  • Participants enrolled: 90
  • From 10 Jan 2024 to the primary completion date, 25 Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Vigilance-modifying drugs (high-dose psychotropics, antispastic drugs)

Other illness

  • Known allergy to of the fNIRS cap components: neoprene

Other

  • Person under tutorship or curatorship
  • No vibrations feeling on the deficient side

Who the study is looking for

  • 18-85 years old
  • Able to sign a consent form
  • Sufficient command of the French language to understand instructions
  • Affiliated to a social security scheme
    • Healthy participants:
  • Right handed
  • No neurological disease or motor deficit
    • Stroke participants:
  • Stroke volunteers in acute phase (before day 14 post-stroke)
  • Not aphasic
  • Able to maintain sitting position without difficulty
  • Deficit moteur
  • Able to sign a consent form

Age in the registry: 18 years to 85 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU d'Orléans
Coordinator of this site? Confirm its status
OrléansFranceUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.