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Recruiting NCT05199896

Touching the World With a Cane: Cognitive and Neural Processes

No phase Interventional Visual Impairment Healthy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Behavioral protocol, EEG protocol, fMRI protocol.
Who it may be relevant to
Registry conditions: Visual Impairment, Healthy. Basic parameters: 18 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Touching the World With a (Blind) Cane: Cognitive and Neural Processes

Overview

The use of tools is ubiquitous in our lives and allows us to expand the sensorimotor capacities of our body. Much research has been done on the subject in sighted people over the past decades. This work has mainly focused on the motor aspect of using the tool, neglecting the sensory aspect. However, any action involving a tool carries sensory information, for example in the use of the white cane by blind people. 26% (\> 200,000) of blind people in France use a white cane to get around. By sweeping the cane on the ground, they use it as a sensorimotor extension of their body to extract information from the environment in order to locate a pedestrian crossing or possible obstacles. While it is well established that the tools increase the user's motor skills, we have only just begun to clarify how they also function as sensory extensions of the user's body and how this phenomenon is potentially dependent on constant use of the tool to compensate for a missing sense, as is the case with blind people using a cane. The aim of this study is to fill this important gap in our knowledge.

Interventions

  • Behavioral Behavioral protocol
    A touch sensitive computer screen either displaying a downscaled (45cm long) image of the rod (for the sighted), or supporting a same sized wooden rod (for the blind), will be placed on the table in front of the participant to record their localization performance. They will be instructed to use their left index fingertip to indicate on the image of the screen (for sighted) or on the wooden rod (for the blind) the position where they have felt the touch provided to the 90 cm long they held in th
  • Device EEG protocol
    The EEG protocol will be similar as the behavioral one described above, with the distinction of taking place in two separate sessions: one where the rod are touched, and one where their hand is touched. The participant will hold a rod in each hand and he will have to indicate on which rod he felt the touch. Additionally electrophysiological responses will be continuously recorded using a 65 channel ActiCap system (Brain Products).
  • Device fMRI protocol
    The same behavioral task and procedures of the behavioral protocol described above will be applied, adapted to take into account the constraints posed by the magnetic environment of the MR scanner. The participant will be placed on the scanner bed and provided with earphones that will both protect against the noise of the machine (80dB) and ensure a continuous communication with the participant. During the fMRI sessions, the participant will solve the same rod localization behavioral task while

Primary outcome measures

  • Perceived location [Time frame: 90 minutes]
Secondary outcome measures (2)
  • Brain activity [Time frame: 6 hours]
  • Brain activity [Time frame: 3 hours]

Eligibility criteria

Inclusion criteria

  • Man or woman, aged 18 to 60 years old
  • Give an informed consent by signature
  • Be part of the national health security system (registered to the Securité Sociale)
  • do not confuse his right and his left

Specific of the non-sighted participants:

  • Loss of vision happened at birth or 3-to 5 years later minimum in life
  • Must have a visual acuity inferior or equal to 4/10
  • Be with a close relation for read information letter and sign the consent form if needed

Exclusion criteria

  • A person presenting an history of neurological, psychiatric or linguistic problems cannot be admitted
  • Assumption of psychotropic drugs
  • Pregnancy or breast-feeding woman
  • A person under legal tutoring
  • A person under care in other medical structure for reasons different from those of this research
  • A person under administrative or judiciary contention
  • A person who is not eligible to a MRI-exam according to the following criteria cannot be admitted to the experiments including MR acquisitions :
  • Have a neurological, cardiac (battery) or defibrillator pacemaker
  • Have a cardiac prosthesis (valve, stent...) or vascular prosthesis
  • Have intracranial clips or clamps
  • Carry a bypass of the cerebrospinal fluid
  • Having metallic splinters in the eyes
  • Wear metal prostheses (teeth, knees)
  • Wear an infusion pump or system
  • Be claustrophobic or have respiratory problems
  • Have metal tattoos close to the head
  • Have permanent make-up

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Basic science

Study locations

France · 1 center
  • Equipe IMPACT du CRNL, Bâtiment INSERM — Bron

Identifiers

NCT: NCT05199896 · 69HCL21_0882

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗